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The Big Physical: Where to Go, What to Get | Departures

October 9th, 2015 6:45 am

While getting old may beat the alternative, living in denial is a comfortable choiceand a lot more pleasant than your first colonoscopy. The annual checkup at your doctors office covers the basics, but a truly thorough medical exam will involve trips to several offices, with the usual long waits and patients stacked up like planes over Chicagos OHare. Two years ago one of my closest friends died from a coronary that absolutely could have been prevented had he only taken the time from his crazy work schedule and family obligations for a checkup.

With baby boomers starting to age, there has been a proliferation of facilities offering comprehensive "executive" physicals. Having just turned 50 myself, I figured this might be a good time to see how the examsand my bodyhave evolved. Among the best-known options, the Mayo and Cleveland clinics, along with the Johns Hopkins, Duke, UCLA, and Stanford units, are all associated with major hospitalswhich is useful should serious complications be found or immediate treatment be recommended. According to the Mayo Clinic, less than 5 percent of its exams revealed potentially life-threatening conditions and almost half exposed risk factors for serious illness. These centers draw patients from all over the world and focus not just on medical needs but a lifestyle approach as well. The Cleveland Clinic even offers programs through the Canyon Ranch spa resorts. Also available are a number of private diagnostic centers that only perform physical exams, such as the Princeton Longevity Center in New Jersey and Texass Cooper Clinics. I chose the PLC strictly for its convenience, but some might be more comfortable going to a hospital. Others prefer to go the true luxury route and turn their physical into a spa holiday or fit it into a resort vacation. To me, though, the chance of getting some bad medical news before my kelp facial could be a real buzz kill.

As at most centers, the day in the PLC started at the scanning facility, replete with state-of-the-art, 64-slice CT machines. I was then shuttled around the main office, given every sort of workup imaginable, and promised a full report on my mortality within hours. Some centers recommend full-body CT scans for patients over 45. While they can be lifesavers, they are also controversial. Dr. Reginald Munden, interim chair of the department of Diagnostic Radiology at the University of Texas M. D. Anderson Cancer Center, says, "Im not comfortable with a shotgun approach to screening," citing the limited sensitivity of scans to common cancer lesions and the small but significant increase in cancer risk from more radiation exposure. There is also the issue of false positives: Up to 80 percent of such tests may find something that can lead to what Munden calls a spiral of expensive and anxiety-provoking follow-up scans with few meaningful results. Interestingly, just as risky can be false negativesbeing told the scan shows no problems to be concerned about. This can lead some people to continue damaging behavior, such as smoking, or to ignore new symptoms.

Of course, there are many stories of serious problems being caught. Doctors at the clinics have received numerous e-mails from patients whose renal cancer or developing aneurysm was detected early, possibly saving their lives. In fact, the day I was at the PLC an exinvestment banker discovered, after 53 years, that he was born with only one kidney. Balancing the risks against the benefits of a scan is a personal decision, and any clinic should provide you with plenty of information to allow you to make an educated evaluation. Dr. Richard S. Lang, who heads the section of preventive medicine at the Cleveland Clinic, explained that while "the scans may not be for everyone," they certainly "offer additional information to a patients profile" and, so long as the findings are managed properly, can be of great valueeven if just as a baseline for future exams.

After the CTs and blood tests are completed, you can expect a very detailed and unrushed physical from a senior staffer instead of the usual Cliffs Notes version offered by your GP. Every aspect of your medical history will be checkedyou will be asked to send copies of all available reports in advanceand any issues, aches, or pains considered. I then had a challenging cardiovascular stress test and gym session with senior exercise physiologist Chris Volgraf. A highly educated trainer and professional strength coach, he completely changed my perspective on my own workout regimen and showed me a series of warm-ups and exercises designed to make my gym time safer, more efficient, and more effective.

Lunch was followed by a vision and hearing test, a bone density and body composition scan, and a meeting with a nutritionist, who evaluated the three-day food log I had been asked to keep.

When all the tests were done, the biggest difference between a full day at one of the clinics and a quick routine maintenance check became clear: A senior doctor sits down with you and reviews the results of every test in detail and their implications. Seeing rotating, 3-D, full-color computer images of your internal organs can be disquieting. Dr. David Fein, medical director and founder of the PLC, told me that one of the most effective tools in convincing patients to modify their unhealthy lifestyle is showing them their blocked arteries or the vascular fat wrapped around their vital organs in high-definition splendor. "You can point to it and say Thats a picture of your heart attack, or your type 2 diabetes diagnosis in five years. " Pushing the predictive envelope, the Duke Executive Health Program will soon offer a cutting-edge genomic DNAbased assessment that screens for certain genetic risks.

I left the PLC with a hefty binder, complete with test results and a disc containing copies of my scans, to give to my personal physician. In my opinion anyone who can afford it, or whose employer or insurer will pay, should immediately sign up for a visit to one of the top clinics and return at reasonable intervals. The Mayo Clinic quotes studies showing that companies can save as much as 20 percent in additional medical claims and 45 percent in extra sick days taken by executives who have regularly undergone thorough physicals. Its unlikely you have ever gotten so complete and detailed a review of not just the results but also the meaning of routine medical tests, as well as specific and practical advice on diet and exercise. While affiliation with a hospital or a major medical clinic is obviously a plus, the most important thing a diagnostic center can do for you is get you in the door. So if traveling makes you less likely to go, pick a center nearby.

centerforpartnershipmedicine.com Location: Chicago, IL Program:1 day Approx. Cost: $3,000$6,000

clevelandclinic.org; executivehealthprogram.com Location: Cleveland, OH; Weston, FL; Toronto; Canyon Ranch (AZ, MA) Program:13 days Approx. Cost: from $3,000

cooperaerobics.com/clinic Location: Dallas and McKinney, TX Program:1 day Approx. Cost: $1,800$4,000

dukeexechealth.org Location: Durham, NC Program:1 day Approx. Cost: $2,800

execmd.com Location: Menlo Park, CA Program:1/2 day Approx. Cost: $2,000$2,600

hopkinsmedicine.org/gim/clinical/executive_health Location: Baltimore, MD Program:1 day Approx. Cost: $1,800$2,200

mayoclinic.org/executive-health Location: Rochester, MN; Scottsdale, AZ; Jacksonville, FL Program:12 days Approx. Cost: $1,500$6,000

theplc.net Location: Princeton, NJ Program:1 day Approx. Cost: $3,250

exechealth.ucla.edu Location: Los Angeles, CA Program:1 day Approx. Cost: from $2,400

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Virginia Diabetes and Endocrinology

October 9th, 2015 6:43 am

Welcome

Our group'smission is to provide personal servicefor patients who have a variety of medical concerns, with an emphasis on Diabetes, Endocrinology, and Internal Medicine. The Physicians withVirginia Diabetes & Endocrinology,P.C.have proudly served the greater Richmond area for over 20 years.

Ourhealth care teamincludes board certified Endocrinologists, Internists, and Nurse Practitioners, as well asa friendly, compassionatesupport staff.Pleaseexplore our website to learn more about Virginia Diabetes & Endocrinology, P.C., our health care providers, and the care and services we offer.

As part of our ongoing effort to provide the highest quality of care, we are proud to introduce our web-based patient portal. This gives patients the opportunity to use the power of the "Web" to track your health care progress in our medical office. We encourage you to take advantage of this new opportunity to play an active role in managing your healthcare.

Visit the portal at health.eclinicalworks.com/vadiabetes To pay your bill on line please click the following link or paste it in your browser https://www.medfusion.net/secure/portal/index.cfm?fuseaction=home.login&dest=paymybill&gid=4116

For patients interested in obtaining individual health and nutrition goals, Specialty Nutrition and Health is arewardingoption. Their Dietitians are available in our Midlothian office. Visit http://www.specialtynutritionandhealth.comto find out more about the practice, their staff and additional locations.

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Arthritis – NHS Choices

October 9th, 2015 6:42 am

Introduction

Arthritis is a common condition that causes pain and inflammation in ajoint.

In the UK, around 10 million people have arthritis. It affects peopleof all ages, including children (see below).

The two most common types of arthritis are osteoarthritis and rheumatoid arthritis.

Osteoarthritis is the most common type of arthritis in the UK, affecting around 8 million people.

It often develops in people who are over 50 years of age. However, it can occur at any age as a result of an injury or another joint-related condition.

Osteoarthritis initially affects the smooth cartilage lining of the joint. This makes movement more difficult than usual, leading to pain and stiffness.

The cartilage lining of the joint can then thin and tissues within the joint can become more active. This can then lead to swelling and the formation of bony spurs, called osteophytes.

In osteoarthritis, the cartilage (connective tissue) between the bones gradually erodes, causing bone in the joints to rub together. The joints that are most commonly affected are those in the hands, spine, knees and hips.

Read more aboutosteoarthritis.

In the UK, rheumatoid arthritis affects more than 400,000 people. It often starts when a person is between 40 and 50 years old. Women are three times more likely to be affected than men.

Rheumatoid and osteoarthritis are two different conditions. Rheumatoidarthritis occurs when the body's immune system targets affected joints, which leads to pain and swelling.

The outer covering (synovium) of the joint is the first place affected. This can then spread across the joint, leading to further swelling and a change in the joint's shape. This can cause thebone and cartilage to break down.

People with rheumatoid arthritis can also develop problems with other tissues and organs in their body.

Read more about rheumatoid arthritis.

Thesymptoms of arthritis you experience will vary depending on the type you have.

This is why it's important to have an accurate diagnosis if you have:

Arthritis is often associated with older people, butit can alsoaffect children. In the UK, about 15,000 children and young people are affected by arthritis.

Most types of childhood arthritis are known as juvenile idiopathic arthritis (JIA). JIA causes pain andinflammation in one or more joints for at least six weeks.

Although the exact cause of JIA isunknown, the symptoms often improve as a child gets older, meaning they can lead a normal life.

The main types of JIA are discussed below. You can also readmore about the different types of juvenile idiopathic arthritis on the Arthritis Research UK website.

Oligo-articular JIA is the most common type of JIA. It affects fewer than five joints in the bodymost commonly in the knees, ankles and wrists.

Oligo-articular JIA has good recovery rates and long-term effects are rare. However, there's a risk that childrenwith the condition may develop eye problems, so regulareyetests with an ophthalmologist (eye care specialist) are recommended.

Polyarticular JIA, or polyarthritis, affects five or more joints. It can develop at any age during childhood.

The symptoms of polyarticular JIA are similar to the symptoms of adult rheumatoid arthritis. The condition is often accompanied by a rash and a high temperature of 38C (100.4F) or above.

Systemic onset JIA begins with symptoms such as a fever, rash, lethargy (a lack of energy) and enlarged glands. Later on, joints canbecome swollen and inflamed.

Like polyarticular JIA, systemic onset JIA can affect children of any age.

Enthesitis-related arthritis is a type of juvenile arthritis that affects older boys or teenagers. It can cause pain in the soles of the feet and around the knee and hip joints, where the ligaments attach to the bone.

There's no cure for arthritis, but there are many treatments that can help slow down the condition.

For osteoarthritis, painkillers,non-steroidal anti-inflammatory drugs (NSAIDs) andcorticosteroids are often prescribed.

In severe cases, the following surgical procedures may be recommended:

Read moreabouthow osteoarthritis is treated.

In treating rheumatoid arthritis, the aimis to slow down the condition's progress and minimise damage to the joints. Recommended treatments include:

Read moreabouthow rheumatoid arthritisis treated.

Arthritis Research UK and Arthritis Careprovide moreinformation about arthritis, as well as advice and support for people living witharthritis.

You can also use the NHS post code search tofind arthritis services in your area.

Page last reviewed: 21/02/2014

Next review due: 21/02/2016

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Graduate Program in Genetic Counseling : Center for …

October 8th, 2015 7:45 am

Northwestern University provides a strong foundation in core genetic counseling skills and identifies each students strengths in order to ignite the passion and lifelong commitment to learning that is critical to professional development. Graduates not only feel extremely capable in multiple clinical settings and specialties, but also recognize how valuable their training has been in preparing them for expanded genetic counseling careers.

Since the inception of the Northwestern University Graduate Program in Genetic Counseling in 1990, the leaders of the program have strived to look to the future of the genetic counseling profession to help guide the overall administration and curriculum. The field of genetics has evolved rapidly over time, and graduate programs need to be aware of the changes that will continue to shape and influence the profession. Northwestern has continued to successfully evolve to meet these changing needs. There are several strengths that allow Northwestern to maintain this cutting edge:

This unique combination, along with the personalized attention a student receives during their training, creates an exciting learning environment and is one of the major strengths of the Northwestern program. We believe our students deserve a strong science, research and psychosocial curriculum.

In addition, Northwestern is proud to offer one of the only dual degree programs available in Genetic Counseling and Medical Humanities and Bioethics.

The combination of the programs nationally recognized faculty, the diversity of clinical and patient experiences, and the cultural excitement of its location in Chicago makes this program unique, exciting and visionary!

Learn more about the program via the links below.

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Graduate Program in Genetic Counseling : Center for ...

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Welcome to the Indiana Institute for Personalized Medicine

October 7th, 2015 6:47 am

Dr. Lang Li, Associate Director of the IIPM, namedDirector ofIU Center for Computational Biology and Bioinformatics. Read more...

IIPM Member Dr. Janet Carpenter named Indiana University Distinguished Professor.Read more...

Posted on August 12, 2014 IIPM Member receives Conquer Cancer Foundation grant Dr. Costantine Albany, IIPM member, has received a Conquer Cancer Foundation grant. Read more...

Posted on July 25, 2013 Educational Conference on Personalized Medicine and Pharmacogenomics "Pharmacogenomics in Clinical PracticeWhat you need to know" Thursday, September 5, 2013 from 8:30am 3:00pm The Indiana Institute of Personalized Medicine is offering a didactic and case-study oriented educational conference focusing on pharmacogenomics and its application in clinical practice.The IIPM, led by Dr. Flockhart and a select group of clinicians and pharmacogenomic experts, will conduct a CME and ACPE qualified program addressing the use of pharmacogenomics in clinical practice. The program will be held at the IU Health Neuroscience Center Auditorium at 355 West 16th Street Indianapolis IN 46202. Read more...

To assist with the recognition of these medications, Dr. Malaz A. Boustani and an interdisciplinary team developed the Anticholinergic Cognitive Burden (ACB) list as a practical tool that identifies the severity of anticholinergic effects on cognition of both prescription and over-the-counter medications. Read more...

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Welcome to the Indiana Institute for Personalized Medicine

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Comprehensive Health Exam :: Princeton Longevity Center

October 7th, 2015 6:46 am

Announcing Our Newest Location in Fairfax, Virginia Call Us for Details!

The Princeton Longevity Comprehensive Exam takes your health beyond the "Annual Physical".

With the latest technology, combined with caring experts who take the time to fully evaluate your health, the Princeton Longevity Center Comprehensive Exam can detect early cancers, heart disease, aneurysms and the "silent killers" that are often missed in a typical physical exam or routine blood tests.

Youll get the latest diagnostic, screening and imaging technologies to assess the state of your health and the detailed information you need to optimize the quality of your future years.

The scope of your examination and the amount of useful information you come away with is dramatically more revealing than a standard physical exam or consultation. The effect on your future can be dramatic.

Our proactive approach to illness and premature aging will help you identify your risk of future disease and create a personalized program to improve your health and maintain an active lifestyle. You'll learn how simple, easy changes in nutrition, fitness, lifestyle and natural supplements can effectively prevent most Cancers and Heart Disease.

You'll receive this total, in-depth evaluation in one day and one place. We'll make you comfortable and look after you every step of the way.

Best of all, you'll get the peace of mind that comes from knowing that you are doing all you can to take care of your health- for yourself and for the people who care about you.

Request an Appointment or More Information

Learn More About the Exam with Frequently Asked Questions About The Comprehensive Exam

Comprehensive Exam Components

Comprehensive Exam Options and Electives

Find out how to use your Health Savings Account or Flex Account for A Comprehensive Exam

The Road Map

We'll explain the results of your evaluations, provide you with a clear understanding of your health issues and create a detailed, customized treatment plan for you. You'll walk out with a practical "road map" you can follow to maintain and enhance your health and fitness on a daily basis.

At the Princeton Longevity Center, we are your partners in long-term health care. When you walk out of our office, our involvement in your well-being does not end, and we will continue to monitor your progress through a choice of Follow-Up Options. This is not just an exam, it's the start of your plan for staying well for the years to come.

The Rewards

A Comprehensive Exam lets you take control of your health. If you are worried about your risk of heart disease, cancer or other health problems, a Princeton Longevity Center Comprehensive Exam can give you the Peace of Mind that comes from knowing that all is well.

Youll know whether or not you are really at risk for heart attack, cancer, diabetes, premature aging or other significant health issues. And, you will find out what you can do about those risks. You'll learn how to prevent cancer, heart disease, diabetes and many other diseases from affecting your future.

You'll have the opportunity to anticipate and prevent illness and premature aging. You'll learn the simple, easy steps that you can take to prevent cancer, heart attacks, diabetes, lung disease, and more. We will show you how you can improve your nutrition and fitness so that your future years are healthier and more active.

The Princeton Longevity Center is focused on helping you with healthy living at the forefront of new medical knowledge and diagnostic technologies. So, you can stop worrying and know that you are doing all you can to optimize your health for today and the years to come.

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Princeton Longevity Center

October 7th, 2015 6:46 am

Sensation 64-Slice CT High Definition Coronary Artery Scans

I don't want to know if something is wrong. Won't the scan make me too nervous?

What type of scaner is used?

What happens during the scan?

What about the radiation exposure?

How long does a scan take?

Do I need to fast?

Do I need a referral from my physician?

Is the scan covered by my insurance?

How accurate is a Heart Scan?

My cholesterol level is normal. Should I still have a Heart Scan?

What if I already know I have heart disease?

I was told the scan can't detect "soft" plaque. Does that matter?

I already passed a stress test. Should I still have a scan?

How does the scan detect coronary artery disease?

What about blood tests like C-Reactive Protein and Homocysteine?

Is this the same scan that I saw on Oprah or in the newspapers?

What do I do with my test results?

What makes the Princeton Longevity Center's scans different from all the other scanning centers that I have seen or heard advertised?

Request an Appointment or More Information Back to Coronary Artery Scan Page

I don't want to know if something is wrong. Won't the scan make me too nervous?

Heart disease is extremely treatable, especially if found early. If your scan shows that you are at risk for developing coronary artery disease, we can show you how simple changes or treatments can dramatically alter your risk and lessen the chances that you will have a heart attack. Avoiding a scan will not stop the disease. Knowing what simple steps you can take will make a big difference in the quality of the rest of your life.

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What type of scanner is used?

Our scans are done with a Siemens Definition AS 64 Slice CT Scanner. This state of the art scanner uses very low radiation doses and produces exceptional detail, as small as 1/50th of an inch. The scans are also extremely fast, usually less than 10 seconds, so there is no need for prolonged breath-holds. The scanner is completely non-claustrophic.

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What happens during the scan? Is it uncomfortable?

64 Slice CT scans are quick, painless and safe. You lie on a table and hold your breath for a few seconds. There are no needles or dyes; it is not claustrophobic and you usually don't even have to remove your clothes.

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What about the radiation exposure?

There has been a lot of attention in the media surrounding the issue of radiation exposure. We keep our doses as low as possible. Our Coronary Calcium Heart Scans generally involve a dose of about 1 mSv, an amount much lower than is typically cited in the media. According to the US Nuclear Regulatory Commission the risk of 1 mSv is about 1 in 25,000 or, put another way, it raises your cancer risk from 20.000% to just 20.004%. On the other hand, your risk of dying from cardiovascular disease that goes undetected and untreated is 36%. We believe that the potential benefit of early detection of cardiovascular or other diseases more than offsets the extremely small potential risk of this level of radiation exposure.

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How long does a scan take?

The heart, lung or whole body scans take just a few seconds. We will spend some time explaining the procedure to you before the scan. You will get your results within a few mintues. Altogether, you should plan on being at our center about 30 minutes.

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Do I need to fast?

No. There is no special preparation or fasting required for heart, lung or whole body scans.

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Do I need a referral from my physician?

No. While many physicians do refer their patients for these scans, we do not require physician referrals. However, we do encourage you to discuss the test with your physician. With your consent, we will send a copy of your results to your physician along with any recommendations for further treatment or testing.

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Is the scan covered by my insurance?

Most private insurance plans will notcover coronary artery scans . In some cases, the coverage will depend on whether the test is done solely as a preventive screening test or to help your doctor make a decision about your treatment.

Medicare Beneficiaries please note: In general, Medicare does not cover preventive services. Coronary Arteries Scans (CPT Code 75571) are specifically a non-covered service. You will not be able to receive any reimbursement from Medicare for these services.

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How accurate is the Coronary Artery Scan?

It is VERY accurate. There are no false-positives. The presence of calcium in the coronary artery means there is plaque there. The relationship between calcium in the artery and the risk of a heart attack has been well established in numerous medical studies. The more calcium present the higher your risk of a heart attack. The absence of any calcium on your scan means you are not at risk for a heart attack with a 99.9% certainty.

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My cholesterol level is normal so why should I bother with a coronary scan?

Study after study has shown that cholesterol levels do NOT accurately predict who will have a heart attack. In fact, 70% of heart attacks occur in people with "normal" cholesterol levels. Even if your cholesterol level is below the current guidelines you can still develop coronary artery disease. With coronary artery scans we can tell if your current cholesterol level is safe for you or if it needs to be lower.

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What if I already know I have heart disease?

Coronary artery scans are useful not only in early detection of disease but also for following the course of the disease. The scan can be used to monitor your treatment with diet, medication, etc. If your treatment is working, the scan will show the improvement. If it is not working, serial scans can show the continuing progression of the coronary artery disease and alert your physician to the need for more aggressive or alternative treatments.

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I was told coronary artery scans can't detect "soft plaque" and isn't that really where the danger is?

While it is true that a coronary artery scan only shows "calcified plaque" and not "soft plaque" (plaque that has not yet calcified), that does not make the scan any less useful. Calcified plaque serves as a marker for the presence of soft plaque. Numerous studies have proven that the coronary artery scan is the most accurate and sensitive predictor of your risk of having a heart attack or significant coronary artery disease. If you don't have any calcified plaque the likelihood that there is any soft plaque is extremely small. No other non-invasive test can detect the presence of early coronary artery disease as well as coronary scans.

If you have a high level of calcified plaque or your clinical history warrants further investigation, a CT Angiography will very reliably detect the presence of soft plaque and measure whether there is a signficant blockage in the arteries.

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I already passed a stress test. Should I still have a scan?

Stress tests only show an abnormality if you have an artery that is at least 65-80% blocked. At that point, treatment may require surgery or angioplasty. And, 70% of heart attacks happen in arteries that are less than 50% blocked and a stress test would not have shown anything wrong. The coronary artery scan can detect developing blockages much earlier, often many years before anything is detectable on a stress test. At that point, treatment with minor changes in diet and lifestyle along with nutritional supplements or medications can be very effective in preventing any worsening of the disease. That can allow you to avoid surgery or invasive procedures later on.

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How does the scan detect coronary artery disease?

The coronary artery scan detects the presence of calcium deposits in the wall of the arteries. These are often present long before blockages have become severe enough to be found by other means such as stress tests. Coronary artery calcium deposits are a "clinical marker" for coronary artery disease. The more calcium present the higher the risk that you may have a heart attack.

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What about blood tests like C-Reactive Protein or Homocysteine levels? Can't they tell if I have heart disease?

There is currently NO blood test that is able to tell if you have coronary artery disease. Blood tests can only estimate your probability of getting coronary disease. Many people with high levels of cholesterol, C-Reactive Protein or Homocysteine do not have coronary artery disease. At the same time, it is common to still get coronary disease even if those tests are normal. Relying solely on those tests means treating a lot of people who do not actually need to be treated and missing a lot of cases where heart attacks could have been prevented. Coronary scans look directly at your own arteries to see if you have a problem or not. Then, treatment is based on what is actually going on in your arteries instead of a statistical "guess".

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Is this the same scan that I saw on Oprah or in the newspapers?

Yes. 64-Slice CT Scans have been prominently featured on many national talk shows and in numerous magazines and other publications.

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What do I do with my test results?

You will get a copy of your test results along with a detailed explanation of the significance of the restuls immediately after your scan. We strongly encourage you to share these results with your physician to seek his/her advice as to any additional treatment that may be recommended.

Our Full Body Scans include a consultation with one of our expert physicians who will also explain the significance of the heart scan results. If you have a Full Body Scan (either with your heart scan or as part of a Comprehensive Exam) you will also get a preliminary review, pending the final report by our radiologist. If you are referred by your physician, the report will be sent to your physician and further management should be discussed with your doctor. If you are not referred by a physician, the discussion of your scan results will include general guidelines for steps you can take to help lower your future health risks.

Imaging studies and other medical tests may reveal findings that require additional evaluation or treatment. THe Princeton Longevity Center does not offer Primary Care or on-going medical management. All findings related to any tests performed at Princeton Longevity Center should be discussed by you with your Primary Care or Family Physician. If additional testing or treatment is warranted this can be arranged through your personal physician. A copy of your results will be sent to any physician you designate.

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What makes the Princeton Longevity Center's scans different from all the other scanning centers that I have seen or heard advertised?

For cardiac scans, the 64-Slice CT Scanner is the "gold standard." The Princeton Longevity Center is the region's leader in Cardiac Imaging and prevention. We don't just do Cardiac CT, we TEACH it. Our physicians have trained over a thousand physicians from around the world at our renowned Cardiac CT Training Course. Our scans are read twice, including our premier experts in cardiac imaging and radiologists expert in body scans. No other cardiac imaging center in the area offers this level of expertise in the interpretation of your results.

The Princeton Longevity Center is the only scanning center in the region that goes beyond scanning. Our staff of expert physicians, nutritionists and exercise physiologists are available to show you how to take the next step with our Comprehensive Exam program.

After we explain your results to you in-depth, our comprehensive preventive medicine center can offer you the tools and resources you need to immediately start to take a proactive role in your health. We work with you and your family physician to design a plan that will quickly start to lower your risk of heart attack and many other life-threatening diseases.

Other scanning centers may be able to tell you if there is a problem. The Princeton Longevity Center will tell you what you can do about the problem and help you take the next step to a healthier future.

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Princeton Longevity Center

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Product Longevity|Freescale

October 7th, 2015 6:46 am

Microcontrollers Kinetis K K02 - April 2014 Microcontrollers Kinetis K K10 - July 2011 Microcontrollers Kinetis K K11 - August 2012 Microcontrollers Kinetis K K12 - August 2012 Microcontrollers Kinetis K K20 - July 2011 Microcontrollers Kinetis K K21 - August 2013 Microcontrollers Kinetis K K22 - April 2014 Microcontrollers Kinetis K K24 - January 2014 Microcontrollers Kinetis K K26 - May 2015 Microcontrollers Kinetis K K30 - July 2011 Microcontrollers Kinetis K K40 - July 2011 Microcontrollers Kinetis K - K50 July 2011 Microcontrollers Kinetis K - K51 July 2011 Microcontrollers Kinetis K K60 - July 2011 Microcontrollers Kinetis K K63 - January 2014 Microcontrollers Kinetis K K64 - January 2014 Microcontrollers Kinetis K K65 - May 2015 Microcontrollers Kinetis K K66 - May 2015 Microcontrollers Kinetis K K70 - July 2011 Microcontrollers Kinetis L KL02 - June 2013 Microcontrollers Kinetis L KL03 - July 2014 Microcontrollers Kinetis L KL04 September 2012 Microcontrollers Kinetis L KL05 September 2012 Microcontrollers Kinetis L KL13 - 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March 2005 Processors PowerQUICC II Pro MPC8360 - March 2005 Processors PowerQUICC II Pro MPC8347 - June 2005 Processors PowerQUICC II Pro MPC8349 - June 2005 Processors PowerQUICC II Pro MPC8321 - May 2006 Processors PowerQUICC II Pro MPC8323 - May 2006 Processors PowerQUICC II Pro MPC8313 - November 2006 Processors PowerQUICC II Pro MPC8314 - September 2007 Processors PowerQUICC II Pro MPC8315 - September 2007 Processors PowerQUICC II Pro MPC8378 - September 2007 Processors PowerQUICC II Pro MPC8379 - September 2007 Processors PowerQUICC II Pro MPC8377 - September 2007 Processors PowerQUICC II Pro MPC8308 - November 2009 Processors PowerQUICC II Pro MPC8306 - March 2011 Processors PowerQUICC II Pro MPC8309 - March 2011 Processors PowerQUICC III MPC8540 - June 2000 Processors PowerQUICC III MPC8541 - July 2001 Processors PowerQUICC III MPC8555 - July 2001 Processors PowerQUICC III MPC8560 - July 2002 Processors PowerQUICC III MPC8543 - September 2004 Processors PowerQUICC III MPC8545 - 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S12ZVL January 2015 Auto MCU 16-bit S12 MagniV - S12ZVM March 2014 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5554 July 2004 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5200 March 2005 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5534 June 2005 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5565 February 2006 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5566 May 2006 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5567 December 2006 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5200B September 2007 Auto MCU MPC5xxx 32-bit Power Architecture - MPC567XF October 2008 Auto MCU MPC5xxx 32-bit Power Architecture - MPC564xB-C October 2011 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5676R October 2011 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5777M December 2014 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5121e January 2009 Auto MCU MPC5xxx 32-bit Power Architecture - MPC563XM January 2009 Auto MCU MPC5xxx 32-bit Power Architecture - MPC551X September 2009 Auto MCU MPC5xxx 32-bit Power Architecture - MPC560XB December 2009 Auto MCU MPC5xxx 32-bit Power Architecture - MPC560xP April 2010 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5668G/E September 2010 Auto MCU MPC5xxx 32-bit Power Architecture - MPC567xK December 2012 Auto MCU 8-bit S08 - S08AWx January 2009 Auto MCU 8-bit S08 - S08LG32 March 2009 Auto MCU 8-bit S08 - S08SGx April 2009 Auto MCU 8-bit S08 - S08ELx September 2009 Auto MCU 8-bit S08 - S08SLx September 2009 Auto MCU 8-bit S08 - S08D November 2009 Auto MCU 8-bit S08 - S08MP16 November 2009 Auto MCU Kinetis EA - EA September 2014 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5553 July 2004 Auto MCU MPC5xxx 32-bit Power Architecture - MPC560xP April 2010 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5645S October 2012 Auto MCU MPC5xxx 32-bit Power Architecture - MPC564xA May 2012 Auto MCU MPC5xxx 32-bit Power Architecture - MPC564xL October 2009 Auto MCU MPC5xxx 32-bit Power Architecture - MPC564xS May 2012 Auto MCU MPC5xxx 32-bit Power Architecture - MPC5668G July 2012 Auto MCU MPC5xxx 32-bit Power Architecture - MPC567xK December 2012 DSP 24-bit DSP DSP56311 - October 2004 DSP 24-bit DSP DSP56321 - February 2005 DSP 24-bit DSP DSP56720 - May 2008 DSP 24-bit DSP DSP56721 - May 2008 DSP 24-bit DSP DSP56724 - August 2008 DSP 24-bit DSP DSP56725 - August 2008 DSP StarCore DSPs MSC8122 - May 2005 DSP StarCore DSPs MSC8156 - November 2008 DSP StarCore DSPs MSC8154 - April 2010 DSP StarCore DSPs MSC8252 - April 2010 DSP StarCore DSPs MSC8254 - April 2010 DSP StarCore DSPs MSC8256 - April 2010 DSP StarCore DSPs MSC8251 - April 2010 DSP StarCore DSPs MSC8151 - June 2010 DSP StarCore DSPs MSC8152 - June 2010 Sensors Accelerometer - MMA3201 January 2000 Sensors Accelerometer - MMA3202 January 2000 Sensors Accelerometer - MMA3204 January 2000 Sensors Accelerometer - MMA2201 May 2000 Sensors Accelerometer - MMA2202 May 2000 Sensors Accelerometer - MMA2204 May 2000 Sensors Accelerometer - MMA2301 May 2000 Sensors Accelerometer - MMA1254 May 2002 Sensors Accelerometer - MMA1260 November 2003 Sensors Accelerometer - MMA1270 November 2003 Sensors Accelerometer - MMA62xx June 2006 Sensors Accelerometer - MMA65xxKW November 2011 Sensors Accelerometer MMA766X - April 2009 Sensors Accelerometer MMA8451Q - February 2010 Sensors Accelerometer MMA8452Q - February 2010 Sensors Accelerometer MMA8491Q - February 2011 Sensors Touch Sensors MPR031 - February 2009 Sensors Touch Sensors MPR121 - December 2009 Analog Audio SGTL5000 - June 2008 Analog Battery Sensor - MM912_637 February 2011 Analog Communication Transceiver - MC33660 October 2011 Analog Embedded Microcontrollers + power - MM908E626 September 2004 Analog Embedded Microcontrollers + power - MM908E624 November 2004 Analog Embedded Microcontrollers + power - MM908E622 September 2005 Analog Embedded Microcontrollers + power - MM912_634 September 2010 Analog Embedded Microcontrollers + power - MM912F634 October 2010 Analog eXtreme Switch - MC33981 (MC12XS2) August 2004 Analog eXtreme Switch - MC33982 (MC12XS2) July 2006 Analog eXtreme Switch - MC33984 (MC12XS2) July 2006 Analog eXtreme Switch - MC10XS3412 October 2008 Analog eXtreme Switch - MC10XS3435 October 2008 Analog eXtreme Switch - MC15XS3400 October 2008 Analog eXtreme Switch - MC35XS3400 October 2008 Analog eXtreme Switch - MC33988 (MC12XS2) August 2010 Analog eXtreme Switch - MC10XS3535 August 2010 Analog eXtreme Switch - MC35XS3500 August 2010 Analog eXtreme Switch - MC09XS3400 March 2012 Analog eXtreme Switch - MC06XS3517 March 2012 Analog eXtreme Switch - MC10XS4200 (MC24XS4) June 2012 Analog eXtreme Switch - MC20XS4200 (MC24XS4) June 2012 Analog eXtreme Switch - MC06XS4200 (MC24XS4) September 2012 Analog H-bridge - MC33887 September 2006 Analog H-bridge - MC33932 January 2009 Analog H-bridge - MC33931 March 2009 Analog H-bridge MC34931 - January 2015 Analog H-bridge MC34932 - January 2015 Analog H-bridge - MC33926 May 2009 Analog H-bridge MC34933 - July 2010 Analog L/HS Switch - MC33879 December 2006 Analog LED Driver MC34844 - October 2008 Analog LED Driver MC34845 - June 2009 Analog LED Driver MC34848 - June 2010 Analog LIN Physical Layer - MC33662 September 2011 Analog LIN physical Layer - MC33663 August 2012 Analog Linear Regulator - MC33730 March 2009 Analog Power Management and user interface MC13783 - April 2006 Analog Power Management and user interface MC13892 - April 2010 Analog Power Management and user interface MC34708 - November 2011 Analog Power Management and user interface - MC34VR500 October 2014 Analog Power Management and user interface MMPF0100 MMPF0100 (Auto) October 2012 Analog Power Management and user interface MMPF0200 MMPF0200 (Auto) February 2014 Analog Powertrain and Engine Control - MC33810 July 2007 Analog Powertrain and Engine Control - MC33800 July 2007 Analog Powertrain and Engine Control - MC33811 July 2008 Analog Powertrain and Engine Control - MC33812 August 2009 Analog Powertrain and Engine Control - MM912_P812 July 2012 Analog Powertrain and Engine Control - MC33816 April 2014 Analog Pre-Drivers - MC33937 June 2008 Analog SBC - MC33989 November 2002 Analog SBC - MC33742 January 2004 Analog SBC - MC33742 June 2008 Analog SBC - MC33910 March 2009 Analog SBC - MC33911 March 2009 Analog SBC - MC33912 March 2009 Analog SBC - MC33904 November 2009 Analog SBC - MC33905 November 2009 Analog SBC - MC33903 March 2011 Analog SBC - MC33907 April 2014 Analog SBC - MC33908 April 2014 Analog Switch Detection Interface - MC33978 January 2015 Analog Switch Detection Interface MC34978 - February 2015 Analog Signal Conditioning - MC33975 February 2005 Analog Signal Conditioning - MC33972 July 2006 Analog Switching Regulator MC34712 - April 2007 Analog Switching Regulator MC34713 - April 2007 Analog Switching Regulator MC34716 - April 2007 Analog Switching Regulator MC34717 - April 2007 Analog Switching Regulator MC34704 - March 2008 Analog Switching Regulator MC34700 - April 2008 RF Land Mobile - AFT09MS031N April 2012 RF Land Mobile - AFT05MS031N April 2012 RF Land Mobile - AFT05MP075N January 2013 RF Land Mobile - AFT09MS007N June 2013 RF Land Mobile - AFT09MS015N December 2013 RF Land Mobile - AFT09MP055N July 2013 RF Land mobile - AFT05MS004N June 2014 RF RF Military MMRF1004N - December 2013 RF RF Military MMRF1005H - December 2013 RF RF Military MMRF1006H - December 2013 RF RF Military MMRF1007H - December 2013 RF RF Military MMRF1008H - December 2013 RF RF Military MMRF1009H - December 2013 RF RF Military MMRF1012N - February 2014 RF RF Military MMRF1014N - March 2014 RF RF Military MMRF1015N - March 2014 RF RF Military MMRF1016H - February 2014 RF RF Military MMRF1019N - March 2014 RF RF Military MMRF2004NB - December 2013 RF RF Military MMRF2005N - October 2014 RF RF Military MMRF2006N - April 2014 RF RF Military MMRF2007N - October 2014 RF RF Military - MMRF2010N June 2015 RF RF Military - MMRF5014H December 2014 RF RF Military - MMRF1020-04NR3 January 2014 RF RF Military - MMRF1304N December 2013 RF RF Military - MMRF1304L December 2013 RF RF Military - MMRF1305H December 2013 RF RF Military - MMRF1306H December 2013 RF RF Military - MMRF1308H March 2014 RF RF Military - MMRF1310H March 2014 RF RF Military - MMRF1315N June 2014 RF RF Military MMRF1316N - June 2014 RF RF Military - MMRF1318N June 2014 RF RF Military - MMRF1320N March 2015 RF RF Power Products - AFIC10275N November 2014 RF RF Power Products - MRF6V2150N February 2007 RF RF Power Products MRF6VP41KH - December 2007 RF RF Power Products - MRF6V14300H September 2008 RF RF Power Products - MRF6V12250H May 2009 RF RF Power Products - MRF6V12500H August 2009 RF RF Power Products MRF6VP121KH - December 2009 RF RF Power Products - MRFE6VP6300H October 2010 RF RF Power Products - MRFE6VP61K25H November 2010 RF RF Power Products - MRFE6VP5600H December 2010 RF RF Power Products - MRF8P29300H February 2011 RF RF Power Products - MRFE6VP8600H September 2011 RF RF Power Products - MRFE6VP100H April 2012 RF RF Power Products - MRFE6VS25N May 2012 RF RF Power Products - MRFE6S9060N/GN March 2007 RF RF Power Products - MRFE6VP5150N June 2014 RF RF Power Products - MRFE6VP5300N June 2014 RF RF Power Products - MRFE6VP61K25N February 2015 RF RF Power Products - MRF8VP13350N May 2015 RF RF Power Products - MRF7S24250N September 2015 Analog Power Management and user interface PF3000 - Jun 2015

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Product Longevity|Freescale

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Research News: New Skin Stem Cells Surprisingly Similar to …

October 6th, 2015 11:45 pm

Scientists have discovered a new type of stem cell in the skin that acts surprisingly like certain stem cells found in embryos: both can generate fat, bone, cartilage, and even nerve cells. These newly-described dermal stem cells may one day prove useful for treating neurological disorders and persistent wounds, such as diabetic ulcers, says Freda Miller, an HHMI international research scholar.

Miller and her colleagues first saw the cells several years ago in both rodents and people, but only now confirmed that the cells are stem cells. Like other stem cells, these cell scan self-renew and, under the right conditions, they can grow into the cell types that constitute the skins dermal layer, which lies under the surface epidermal layer. We showed that these cells are, in fact, the real thing, says Miller, a professor at the University of Toronto and a senior scientist in the department of developmental biology at the Hospital for Sick Children in Toronto. The dermal stem cells also appear tohelp form the basis for hair growth.The new work was published December 4, 2009, in the journal Cell Stem Cells.

Stem cell researchers like to talk about building organs in a dish. You can imagine, if you have all the right playersdermal stem cells and epidermal stem cellsworking together, you could do that with skin in a very real way.

Freda D. Miller

Though this research focuses on the skin, Miller has spent her career searching for cures for neurological diseases such as Parkinsons. About a decade ago, she decided to find an easily accessible cell that could be coaxed into making nerves. Brain stem cells, some of which can grow into nerves, lie deep in the middle of the organ and are too difficult to reach if the scientists eventually wanted to cultivate the cells from individual patients. I thought, This is blue sky stuff, but you never know. She searched the literature and found that amphibians can regenerate nerves in their skin. She also found published hints that mammalian nerve cells could do the same.

Her team looked in the dermal layer of the skin in both mice and people. Hair follicles and sweat glands are rooted in the dermis, a thick layer of cells that also help support and nourish blood vessels and touch-perceiving nerves. In 2001, Millers team hit paydirt when they discovered cells that respond to the same growth factors that make brain stem cells differentiate. She named them skin-derived precursors (SKPs, or skips).

Miller soon discovered that the cells act like neural crest cells from embryosstem cells that generate the entire peripheral nervous system and part of the headin that they could turn into nerves, fat, bone, and cartilage.That gave us the idea that these were some kind of embryonic-like precursor cell that migrated into the skin of the embryo, Miller said. But instead of disappearing as the embryo develops, the cells survive into adulthood.

Even though the SKPs acted like stem cells in Petri dishes, Miller didnt know if they behaved the same way in the body. We were obviously very excited about these cells, she said. The problem was, cells can do all kinds of weird things in culture dishes that look right but really arent. We thought, Maybe were being deceived.So lab member Jeffrey Biernaskie put the cells through their paces, performing a series of experiments to test whether the SKPs indeed acted like stem cells in the body.

Earlier work in the lab had shown that the SKPs produce a transcription factor called SOX2, which is produced in many types of stem cells. The team used genetically engineered mice with SOX2 genes tagged with green fluorescent protein, which allowed them to track where SOX2 was expressed in the animals. They found that about 1% of skin cells from adult mice contained the SOX2-making cells, and they were concentrated in the bulb at the base of hair follicles.When the team cultured these cells, they began behaving like SKPs.

Next, the scientists decided to see if the cells would not just settle at the base of hair follicles but grow new hair. They took the fluorescent cells, mixed them with epidermal cellswhich make up the majority of cells in a hair follicleand transplanted the mixture under the skin of hairless mice. These mice began growing hair, and analysis showed the green cells migrated to their home base in the bulb of the new hair follicles. The team also transplanted rat SKP cells under the skin of mice. The cells behaved exactly like dermal stem cellsthey spread out through the dermis and differentiated into various dermal cell types, including fat cells and dermal fibroblasts, which form the structural framework of the dermal layer. Intriguingly, the mice that carried transplanted rat SKPs also grew longer, thicker,rat-like hair, instead of short, thin mouse hair. These cells are instructive, they tell the epidermal cellswhich form the bulk of the hair follicleto make bigger, rat-like hair follicles, Miller said. There are a lot of jokes in my lab about bald men running around with rat hair on their heads.

Finally, the team gave mice small puncture wounds and then transplanted their fluorescent SKPs next to the wound. Within a month, many transplanted cells appeared in the scar, showing they had contributed to wound healing. The SKPs were also found in new hair follicles in the healed skin.

The cells behavior both in wound healing and hair growth led the team to conclude that the SKPs are, in fact, dermal stem cells. Miller said the finding complements work by HHMI investigator Elaine Fuchs, who found epidermal stem cells, which help renew the top layer of skin. Combining the evidence from the two labs suggests a possible path to baldness treatments, Miller saidthe dermal stem cells at the base of the hair follicle seem to be signaling the epidermal cells that form the shaft of the follicle to grow hair. But much about the signaling mechanism remains unknown.

Miller wants to investigate less cosmetic applications, such as treating nerve and brain diseases. Experiments she published between 2005 and 2007 showed that SKPs can grow into nerves and help repair spinal cord damage in rats. Her lab is continuing to pursue that research. She is also searching for signals that could trigger the dermal stem cells to rev up their innate wound-healing ability. If such a signal can be found and mimicked, Miller can envision one day treating chronic woundssuch as diabetic ulcerswith a topical cream. Such a treatment is years or decades away, she said, but now researchers know which cell types to focus on. Another possibility: improving skin grafts, which today consist of only epidermal, not dermal, cells. While skin grafts can dramatically help burn victims, those grafts dont function like normal skin.

Stem cell researchers like to talk about building organs in a dish, said Miller. You can imagine, if you have all the right playersdermal stem cells and epidermal stem cellsworking together, you could do that with skin in a very real way.

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Research News: New Skin Stem Cells Surprisingly Similar to ...

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Fat Stem Cells Induce New Hair Growth in Hair Loss …

October 6th, 2015 2:46 am

Earlier this week, researchers from Yale University demonstrated a connection between fat derived stem cells (fatty or adipose stem cells) and hair follicle stimulation and new hair growth in mice.

During the experiment, the team found a correlation between the number of precursor fat cells (fatty stem cells) surrounding hair follicles and the number of follicles capable of entering the anagen growth phase and producing terminal hairs in mice.

In fatty stem cell deficient mice (with little to no fat cells surrounding the hair follicles), the follicles remained in the dormant, telogen phase and caused noticeable baldness. The researchers injected these deficient mice with fat (containing the fatty stem cells) derived from healthy donors and found normal follicle function and new hair growth within two weeks.

According to the research team, the new hair growth and reversal of follicle dormancy, which was noted in 86% of resting hair follicles treated with the injected stem cells, is likely caused by a platelet derived growth factor produced by the fatty stem cells in amounts 100 times greater than the average cell.

In an interview with BBC news, Dr. Valerie Horsley, a member of the Yale research team, claimed:If we can get these fat cells in the skin to talk to the dormant stem cells at the base of hair follicles, we might be able to get hair to grow again.

At this point in time, the researchers claim these results are seen exclusively in mice and may not be reproduced in human trials. However, the study definitely represents an exciting development in the search for non-invasive, cellular-based hair loss treatments.

To review the published study, click here. _______________ Blake Bloxham formerly Future_HT_Doc

Editorial Assistant and Forum Co-Moderator for the Hair Transplant Network, the Hair Loss Learning Center, the Hair Loss Q&A Blog, and the Hair Restoration Forum

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Technorati Tags: stem cells, adipose stem cells, hair follicle, precursor fat cells, fatty stem cells, anagen growth phase, baldness, hair growth, injected stem cells, hair loss

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Fat vs. Bone Marrow Stem Cells in Orthopedics: More …

October 6th, 2015 2:46 am

Fat vs. Bone Marrow Stem Cells in Orthopedics: More Research Showing Marrow is Better

We dont much care where you get your stem cells, as long as the source of the stem cells matches the tissue youre trying to repair. Theproblemwith stem cells is that certain sources produce stem cells more capable of repairing certain tissues and stem cells from other sources are less capable. The general rule of thumb is, the closer the stem cells are to the structure in need or repair, the better they are at repairing that area. This makes sense at face value, as these resident stem cells in all of our tissues have a role inmaintainingand repairing that local organ or tissue. As an example, fat stem cells from your belly or thigh would be good at repairing the local tissues like skin, nerves, blood vessels, etcSo it wasnt surprising to see yet another study showingthatbone marrow stem cells are better at repairing bone than fat based stem cells. This fits with many other studies showing that bone marrow stem cells are much better at repairing orthopedic tissues than fat derived stem cells. This again makes sense, as why would stem cells from belly fat have any role in repairing bone? At the end of the day, rooting for one type of stem cell because thats all the doctor knows how to harvest is like rooting for only one stem cell sports team and not recognizing that all stem cell teams have their positives andnegatives. For example, stem cells derived from fat are much better for cosmetic work and structural fat grafts than stem cells derived from bone marrow. So why fit a square peg into a round hole or use a hammer when a wrench is needed? Use the stem cell source that fits the job!

Disclaimer: Like all medical procedures, Regenexx Procedures have a success & failure rate. Not all patients will experience the same results.

If you liked this post, you may really enjoy this book by the same author - Dr. Chris Centeno

Written by Regenexx Founder, Dr. Chris Centeno, this 150 page book explains the Regenexx approach to patients and orthopedic conditions. Whether youre are an existing patient or simply interested in the human body and how everything in the body ties together, you will enjoy exploring this book in-depth. With hyperlinks to more detailed information, related studies and commentary, this book condenses a huge amount of data and resources into an enjoyable and entertaining read.

Chris Centeno, M.D. is a specialist in regenerative medicine and the new field of Interventional Orthopedics.

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Fat vs. Bone Marrow Stem Cells in Orthopedics: More ...

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Healthy Life Style | Nuclear Medicine | Sports Medicine …

October 5th, 2015 11:45 pm

The specific Water Diet continues to be around for a lot of years, however, many individuals dont know precisely what it is or maybe it could operate. Many people accept it includes upgrading foods along with standard water this really is not situation whatsoever.

Within this publish well review two most important items to request from the diet : Does the concept perform? and Is that secure?A

Before we must prospects questions, we will very first time over just what it requires.

Many people think about the actual Water Diet involves fasting which h2o may for whatever reason switch the harmful link between refusing to eat completely. This is not the reality. Starting a fast isnt a secure or possibly wholesome, too as with fact a effective ultimately, method of weight reduction. Growing h2o consumption while beginning a quick will not choose mtss is a secure method. Virtually no dietary expert can suggest fasting like a weight-loss approach, whether using standard water in addition to without any, for a simple reason. Thank heavens, beginning a quick has virtually no element inside a Water Diet.

Do you know the Water Diet is actually, quite simply, is going to be consuming a lot of h2o although getting generally in addition to furthermore carrying out a couple of other healthy diet. One such technique is that you could eat generally in addition to drink an 8-oz wine glass of chilly standard water shortly in front of a treat, another throughout but a different one particular next. This really is known as the specific Before, Through after Diet program. A little deviation with this particular, together with regarded as a far more effective technique, would be to merge the river getting getting an infinitely more standard eating routine that has been urged from your nutritional expert. Regardless, the most crucial part of nearly water Weight loss program is that a minimum of nine 8-oz portions of chilled water are often consumed every day.

Initially no appear a good way to slim down naturally. In the end, how do h2o cause fat loss? Nonetheless, you will find a couple of appear main reasons why it could operate along with a couple of reserach has shown it truly does impact body fat loss.

Your quest under consideration have been made by Veterans administration Technology in addition to continues to be revealed in the Countrywide Ending up in the U . s . states Compound Culture (ACS) through the mature author Brenda Davy, Ph.D. Your studies shown that grown ups which loved two glasses of standard water just before their foods, although consuming a small calorie eating routine, ate roughly Three several weeks energy a more compact amount through the meal. Throughout the time of three several weeks individuals who loved h2o dropped around 44% more importance (regarding Five pounds) than the others whom did not.

Basically probably the most plausible idea is the fact by blocking your gutters system along with h2o, you will not appetite as much to see happy that leads that you simply very easily eating considerably less. Another excuse folks believe a Water Diet will work is the fact simply by consuming lots of chilled h2o, the body must burn much more calories to be able to warm the forest in your temperature. While this is often indeed correct, just how much calories found in this method is not a good deal and will not have a very important effect on fat loss.

So, thats exactly what it is and how it truly is prone to function, nonetheless should it really work? Effectively, rapid (as well as unhelpful) option would be it depends. For many its been extremely effective too for others, not necessarily. Ths issue it seems would be the number of water which must be consumed. Lots of people sense uncomfortable as well as bloated and coupled with a lot more regular toilet visits, thats sufficient that you should dissuade these.

For many people nevertheless, it may cause good results. Most likely probably the most striking instance, as stated by the media, wound up being Forty one year-old Blake Silva. After getting a quantity of not effective diet plans and evaluating 260 pounds, he soon started a In front of, Throughout after consuming habits where he states hell have had completely normally nonetheless loved roughly 10 servings of h2o each day. Around more efficient several days he missing 70 kilos. There have been another studies regarding accomplishment furthermore, but less than as spectacular, considering the variety of body weight dropped various substantially between varying people.

Consequently, everyone knows that it could benefit several, nonetheless would be the Water Diet secure? Effectively, fortunately, its. Although getting sinking can certainly, inside a couple of uncommon cases, be harmful, it takes much more when in comparison with 7 glasses being consumed being hazardous. The truth is, its perfectly balanced as well as ideal for a persons body. Benefits of consuming much more h2o incorporate, yet others, supporting your body to detox, improving your state of health in addition to attention in addition to aiding you gaze healthy and youthful by striving to help keep the epidermis replenished with water.

Lastly, will it do that eventually? Correctly, like every diet program, itll simply lead to lengthy-term modifications if you do not return to unhealthy behavior as well as existence style that cause transporting excess body fat to begin with. Thats to not express you need to stay with a continuous weightloss routine nevertheless. The simplest approach to conserve a wholesome body weight would be to eat healthy meals and workout. You will find numerous excellent content devoted to fitness well, i wont enter depth but consuming a good deal veggies and fruits and steering clear of fatty meals is a great strategy to begin. Integrating this type of utilizing a good minor working out, including walking every day, means you are around the best track to be able to remaining from the necessity for virtually every future diets.

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Multiple Sclerosis Stem Cell Treatment Panama …

October 5th, 2015 4:49 am

First Symptoms Ms Blog Dec 15, 2014 MS patients need to understand how symptoms appear and disappear. The first year after my MS diagnosis, I was constantly wondering if the In the months before Apple announced Apple Music at an event in San Francisco on June 8, the company had extensive talks with Universal, Sony and Warner, the three major labels, and

Stem cell therapy: Treatment for autism, autoimmune disease, cerebral palsy, heart failure, multiple sclerosis, osteoarthritis, rheumatoid arthritis and spinal cord

Mar 17, 2015 Over the years, many alternative and quack treatments for autism, cancer, and spasticity, pain, spasms, and bladder dysfunction in multiple sclerosis patients . stem cell therapy you have to travel out of the country for this expensive, dangerous, and unproven therapy, o

Patients protest as head of research council says there is no evidence that procedure is effective or safe Costa Rica has cracked down on a stem cell clinic which offered patients experimental treatments diseases such as multiple sclerosis and diabetes.

Multiple Sclerosis Nastursal Healing NK Vue is a unique ELISA-based blood test that measures Natural Killer and cancer surveillance post-treatment, and also to provide additional insights into the condition of active autoimmune diseases such as multiple sclerosis and inflammatory bowel The Maharishi Ayurveda SM Approach to Multiple Sclerosis. Guests often ask, "Can MS respond to the natural approaches of Maharishi Ayurveda?" Our

Complete the FREE CONSULTATION Form To See If You Qualify For Stem Cell Therapy At World Stem Cells Clinic Or Have Questions! Stem Cell Therapy At World Stem

They say it can be used to treat multiple sclerosis, strokes and diabetes. Hundreds of international medical tourists have come to this Central American nation seeking adult stem cell treatment in Costa Ricas neighbor to the south, Panama, claiming

RMI will offer non-surgical stem cell treatments and stem cell enhanced surgeries MPI and SCI are currently conducting seven IRB-approved clinical trials in Panama for autism, multiple sclerosis, rheumatoid arthritis and osteoarthritis using human

Advancells provides Stem Cell treatment as a potential therapy for different diseases. Ask us for cure help in Delhi, India, Bangladesh, Pakistan, Australia, USA , UK.

Jun 18, 2012 Stem Cell Treatment with Beyond Cells is exactly what actor Danny Glover received during his visit. Danny knows the positive impact stem cell therapy has

Stem Cell Therapy. Stem cell treatment and stem cell therapy may be considered controversial and are, perhaps, viewed as akin to science fiction by some people.

Chuck Norris is the star a subsidiary of Medistem Panama, received authorization in April to begin phase one and two of clinical trials using human umbilical cord-derived stem cells for the treatment of multiple sclerosis. The building, cumulative

Thanks for the overview and synopsis on the Stem Cell front, Marc. Just as with the hope for CCSVI, from our anecdotal reported results, it seems to have helped very

Clevelands top medical facilities are collaborating on the nations first clinical trial that uses adult stem cells to treat multiple sclerosis. Four patients damage to the nervous system caused by MS. In the trial, stem cells are taken from

They say it can be used to treat multiple sclerosis, strokes and diabetes. Hundreds of international medical tourists have come to this Central American nation seeking adult stem cell treatment in Costa Ricas neighbor to the south, Panama, claiming

Multiple Sclerosis Stem Cell Treatment Panama 5 out of 5 based on 14 ratings.

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Princeton Longevity Center Review – Health care center …

October 5th, 2015 4:47 am

Princeton Longevity Center Information

Princeton Longevity Center helps you prevents cancers and heart attacks, live longer, look and feel younger. Medicine has changed dramatically in the last forty years. Therefore, why are you still relying on your father's annual physical to stay well.

Services of Princeton Longevity Center

Our healthcare center provides state-of-the-art diagnostic facilities and a level of personal time, care and attention that is unmatched. Our healthcare center also offer a wide array of programs designed to meet the unique needs of busy corporate executives.

Our healthcare center equipped modern equipment such as 4-Slice CT Heart Scans and 3-D Virtual Colonoscopy our exams are able to detect the earliest evidence of the leading causes of death and disability years before any other tests. This will help our healthcare center to identify early and find appropriate treatment for you.

In addition, the best of all, while the Princeton Longevity Center's Executive Exams are the most comprehensive and effective you can find, we are also the most cost-effective. We commit that you will satisfied about cost and service while treatment

Contact Information

Center Name: Princeton Longevity Address: 136 Main Street, Forrestal Village Princeton, New Jersey 08540 Phone Number: 888-8000-PLC (toll-free) or (888.800.0752) Website: http://www.theplc.net Working Hours: For more information call (888.800.0752) or fax (609)430-8470

If you are unsatisfied about this center you can refer toHealth Care District of Palm Beach County. Read moreHealth Care District of Palm Beach County Reviews here.

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Longevity for You

October 5th, 2015 4:47 am

A holistic approach to autoimmune diseases! Click here for more information.

Stephen Lau

For more information, click here.

Longevity is the quest of many individuals. To live a long life and yet remain physically, mentally, and spiritually healthy is a challenge requiring great wisdom.

A long lifespan is a blessing, which has to be earned with the wisdom of an anti-aging healthy lifestyle.

Your Creator has given you the innate wisdom to live long, and your mission in life is to earn those extra years.

The objective of this site is two-fold:

To share with you my own experience of an autoimmune disease, and my self-awakening from that experience.

To share with you my search for health information on natural healing and

My mission is to provide you with

Your mission is to earn those extra years through a healthy longevity mindset to live an anti-aging and lifestyle. Longevity is for you, if, indeed, it is your passionate quest in life.

This is not a mission impossible: if there is a will, there must be a way.

You will be imbued with passion to live a longer tomorrow by changing not only your attitudes but also your lifestyle through a wealth of health information to accomplish your mission to earn your extra years.

Yes, the road to longevity may be long and winding, and even bumpy at times. But you need not fasten your seat-belt to the past or to the present (whatever the state of health you may be currently in). Rest assured, this site will continue to update you with new health information needed to earn your extra years. At the end of t-he day, you will be proud of yourself that you have a credential of living long that few would even dare to contemplate.

Stephen Lau

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Longevity for You

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Neuroscience for Kids – The Eye and Its Connections

October 5th, 2015 4:46 am

Our visual systems perform all kinds of amazing jobs, from finding constellations in the night sky, to picking out just the right strawberry in the supermarket, to tracking a fly ball into a waiting glove. How do our eyes and brains recognize shape, movement, depth, and color? How do we so easily pick a friend's face out of a crowd, yet get fooled by optical illusions? In this first of three units on the Sense of Sight, we consider the anatomy and physiology of the eye, especially the retina, and the initial pathways visual information takes to the brain. Part 2 discusses how various aspects of a visual scene are processed at higher levels, and Part 3 delves into color vision.

1. Our eyes allow us to perceive electromagnetic radiation reflected from objects

Most animals and many plants are photosensitive; that is, they can detect different light intensities. Some organisms accomplish this with single cells or with simple eyes that do not form images but do allow the organism to react to light by moving toward or away from it. In order for an eye to transmit more information about the world, however, it must have a way of forming an image, a representation of the scene being viewed.

Higher invertebrates and virtually all vertebrates have complex, image-forming eyes, and we will "focus" on the refracting eye found in the octopus and in all vertebrates. Arthropods have compound eyes, which have greater depth of focus than refracting eyes, but which sacrifice resolving power or acuity. Our eyes, like those of many animals, detect a just narrow range of all the wavelengths of electromagnetic radiation, that between 380 and 760 nanometers. This range of light is called the visible spectrum. Figure 1 shows how the visible spectrum fits into the entire electromagnetic spectrum.

Figure 1. The electromagnetic spectrum and the visible spectrum.

2. The eyeball is an optical device for focusing light

The mammalian eyeball (Figure 2) is an organ that focuses a visual scene onto a sheet of specialized neural tissue, the retina, which lines the back of the eye. Light from a scene passes through the cornea, pupil, and lens on its way to the retina. The cornea and lens focus light from objects onto photoreceptors, which absorb and then convert it into electrical signals that carry information to the brain. Two pockets of transparent fluid nourish eye tissues and maintain constant eye shape: these are the aqueous and vitreous humors, through which the light also passes. The lens projects an inverted image onto the retina in the same way a camera lens projects an inverted image onto film; the brain adjusts this inversion so we see the world in its correct orientation. To control the images that fall upon our retinas, we can either turn our heads or turn our eyes independently of our heads by contracting the extraocular muscles, six bands of muscles that attach to the tough outside covering, or sclera, of the eyeball and are innervated by cranial nerves. See Table 1 for a brief list of eyeball components and their functions.

The cornea and lens bend or refract light rays as they enter the eye, in order to focus images on the retina. The eye can change the extent to which rays are bent and thus can focus images of objects that are various distances from the observer, by varying the curvature of the lens. The ciliary muscle accomplishes this by contracting to lessen tension on the lens and allowing it to round up so it can bend light rays more, or relaxing for the opposite effect. This ciliary muscle is smooth or non-voluntary muscle-you cannot "decide" to contract or relax it as you do the skeletal muscle in a finger or facial muscle.

Figure 2. The mammalian eyeball.

3. Refractive errors in the eye cause focusing problems

Refractive errors occur when the bending of light rays by the cornea and lens does not focus the image correctly onto the retina. An eyeball that is too long or too short for the optics of the cornea and lens or an irregularly shaped cornea can cause refractive errors, which include myopia (near-sightedness), hyperopia (far-sightedness), and astigmatism. Myopia results either when the eyeball is too long or when the cornea is curved too much, and the focused image falls in front of the retina. Hyperopia is the opposite, with the image falling behind the retina. Astigmatism results from a cornea that is not spherical. Fortunately, most refractive errors can be corrected with prescription lenses.

4. The retina originates from the brain and contains photoreceptors for detecting light

The eye is formed during embryonic development by a combination of head ectoderm and neural tube tissue, the latter forming the retina. Thus, the retina is not a peripheral sensory organ like skin touch receptors or taste buds on the tongue, but rather it is an outgrowth of central nervous tisse. Because of this origin, the retina has layers of neurons, internal circuits, and transmitters characteristic of the brain: it is a bit of the brain that has journeyed out, literally, to have a look at the environment.

The photoreceptors in the retina are of two types: rods and cones, so named because of their shapes. These cells are actually specialized neurons that detect light. Embedded in stacks of cell membranes in the distal portions of rods and cones are molecules that absorb certain wavelengths of light. These molecules are called photopigments and are composed of two parts: a large trans-membrane protein, an opsin, and a smaller chromophore, which is a metabolite of Vitamin A called 11-cis-retinal. The chromophore, which is embedded in the opsin, absorbs light; in so doing it undergoes a shape change. This shape change in turn activates the opsin, setting off a cascade of events that leads to a change in the electrical state of a rod or cone cell membrane. This change in the rod or cone cell membrane is then conducted via the rod or cone axon to other neurons in the retina, and from there to the brain.

5. Rods function in dim light

In dim light, we use our rods, which cannot work in bright light. Rods outnumber cones (120 million rods and about 6 million cones in each retina) and they amplify a light signal much more than cones. Scientists have demonstrated that absorption of even a single quantum (or photon) of light can trigger a chromophore shape change in one molecule of rhodopsin in a rod, leading to signal transmission. For transmission to occur, this initial tiny event must be amplified: the activated molecule of rhodopsin converts several thousand molecules of the next enzyme in the cascade to the active form, and this amplification continues until the electrical potential of the cell membrane changes and neurotransmitter release is affected. Cones, on the other hand, must each absorb hundreds of photons in order to send signals.

Another retinal mechanism that helps us to see in dim light or to see a tiny amount of light in the dark is the convergence of rod cell signals onto other retinal neurons. Many rods (up to 150) synapse onto the same target neurons, where the signals are pooled and reinforce one another, increasing the ability of the brain to detect a small amount of light. (A synapse is a contact between a neuron and another cell where an electrochemical signal [most commonly] is transmitted to the second cell.) This convergence amplifies weak signals, but spatial resolution is lost because rod responses are averaged. That is, we cannot see fine detail using rods.

In order for our eyes to make the transition to dim light, rods must adapt after being saturated with light in brighter conditions. Dark adaptation of rods takes seven to ten minutes: during this time rhodopsin molecules, in which the chromophore components have changed to the activated state, return to the non-activated state so that they are able once again to register changes in illumination. Other changes also occur in adaptation to dark or dim conditions, including enlarging or dilating of the pupil, which is controlled by the autonomic nervous system.

6. Cones mediate day vision

Our vision in bright or moderate light is completely mediated by cones, which provide color vision, black and white vision, and high acuity, the ability to discern fine detail. Like rods, cones contain an opsin and the chromophore 11-cis-retinal, but the opsins differ from rhodopsin so that each cone is responsive to one of three colors: red, green or blue. Cones are spread throughout the retina but are especially concentrated in a central area called the macula. At the center of the macula is the fovea, where only cones (no rods) are found, and these are densely packed. When we want to read or inspect fine detail, we move our heads and eyes until the image of interest falls onto the fovea. Because the fovea lacks rods, it is easier to see in dim light by looking to the side of an object instead of directly at it. You can test this by looking to the side of a faint star so that its image falls on rods, rather than on the fovea where it probably will not register. When you look directly at the faint star, it disappears.

In contrast to the wiring of rods, only a few cones converge onto other retinal neurons to average their signals, so cones provide better spatial resolution. In fact, each cone in the fovea synapses onto only one neuron in the next relay in the retina. This gives this area the ability to transmit fine detail, such as we use in reading.

Thus, cones mediate day vision and rods take over in dim light and at night. Both rods and cones can operate at the same time under some conditions: in dim or dark conditions, rods are most sensitive, but cones respond to stimuli that are sufficiently bright. This is why we can see the colors of neon lights on dark nights.

7. Visual information travels from retinal ganglion cells to the brain

After converting light into electrical signals in their cell membranes, rods and cones transmit this information to other neurons in internal circuits in the retina for processing. From these cells, messages go to the final retinal station, the ganglion cells, whose axons exit the eyeball at the optic disc and form the optic nerve, which contains about one million axons. Because all the nerve fibers converge at the optic disc, no rods or cones are in this area and it forms a "blind spot" on the retina: this may be easily demonstrated in a classroom activity.

Within the optic nerve, a defined group of axons from each eye crosses over to join the opposite optic nerve at the optic chiasma (see Figure 3), so each side of the brain receives visual information from both eyes. After the chiasma, retinal axons go to one of three areas: two of these are in the midbrain and one is in the thalamus. The information going to the midbrain does not reach conscious levels but rather produces pupillary reflexes (which are controlled by the autonomic nervous system) and eye movements. In the thalamus, ganglion cell axons transmit signals to neurons in the lateral geniculate nucleus (LGN) where information is processed and then carried by LGN axons to the primary visual cortex in the occipital lobe of the cerebrum. These cortical cells then send messages to other "higher" cortical areas. Figure 3 shows the anatomy of this system (the midbrain areas are not shown here).

Figure 3. The visual pathway

8. We have an area of central or focused vision and an area of peripheral vision within our fields of vision

The visual field is defined as the view seen by the two eyes while looking straight ahead (Figure 4). Without moving eyes or head, a person can see details (well enough to read) within a limited angle drawn from a point between the eyes on the forehead and two experimentally determined points to the left and right in front of the viewer, at proper focal distance. In addition to this area of clear or central vision, we can see objects and movements to the sides of our heads, although as the distance around to the sides increases, it becomes more difficult to identify objects. The area of central vision includes objects whose images fall onto the central area of the retina, the macula, and especially the fovea (defined above). Cones in all other areas of the retina are in the periphery, and while they convey visual information, they do not provide the resolving power of the densely packed fovea.

Figure 4. Complete visual field and central visual field, looking down onto the head. The complete visual field is the entire area in front of the eyes from the end of one lateral dashed line to the other (including the central visual field).

In addition to speaking of a central and a peripheral field of vision, we can divide these fields by a vertical line down the middle into right and left visual fields. Because of the way ganglion cell axons cross at the optic chiasma, information from the entire right visual field (to the right of a vertical line) goes to the left LGN, and from the left LGN, all axons go to the left occipital cortex (Figure 3). Similarly, all left visual field information goes to the right occipital cortex. Remember that although each visual cortex receives information only from the opposite visual field, this information is collected by defined parts of both eyes.

9. Projections from the retina to the brain generate retinotopic maps

As in the touch sensory system (and to some extent, other sensory systems), visual information is mapped in an orderly fashion onto neurons in the LGN of the thalamus. Further, this topographic mapping continues when LGN neurons carry signals to the visual cortex. As in the touch system, the mapping of the visual field is not isometric; that is, not every area of the visual field is represented in proportion to its size. Rather, the density of sensory neurons in a given area of the retina determines how many central neurons are devoted to that retinal area, as in the touch system where fingertips and lips have a much larger representation in the parietal cortex than do trunk and arms. In the LGN and primary visual cortex, about half of the neurons receive input from the fovea (the eye's "fingertips") and area just around it, where cones are densely packed and visual acuity is highest.

10. Defined groups of neurons in the primary visual cortex process different aspects of visual information

Several attributes of visual information go to the primary visual cortex: motion, form or shape, and color. These aspects of the visual scene travel to different modules or groups of cortical cells (some are given names such as "columns" or "blobs.") In order for us to perceive and interpret these kinds of visual information, other brain areas beyond the primary visual cortex must process the signals and put the visual scene back together.

11. Problems in different parts of the visual system can cause blindness

People who lose cone vision are legally blind, whereas loss of only rod function results in night blindness. Legal blindness is defined as 20/200 vision or worse; that is, a person is considered legally blind if he or she must be 20 feet away to see an object that a person with normal vision can see at 200 feet. Some forms of blindness result from damage to both rods and cones, while others originate with problems in different parts of the visual system. For example, people with damage to particular parts of the cerebral cortex lose specific aspects of vision, such as ability to see parts of the visual field, or to perceive motion, or to recognize faces. More information on these types of visual defects is given in Part 2 of this unit on the Sense of Sight.

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Regenerative Medicine and Stem cell based Cell therapies …

October 4th, 2015 7:41 pm

Information contained on this page is provided by an independent third-party content provider. WorldNow and this Station make no warranties or representations in connection therewith. If you have any questions or comments about this page please contact pressreleases@worldnow.com.

SOURCE Reportlinker

NEW YORK, Oct. 1, 2015 /PRNewswire/ -- Innovative Therapies for treating diseases are being sought after with fresh vigor as new targets, approaches and biology is discovered. Improved health care, nutrition and preventive medicine in the last few decades have all helped in increasing the life expectancy WW. However, this has not translated into any reduction in the incidence or prevalence of chronic or critical illnesses! On the contrary the incidence of chronic diseases like diabetes, obesity, arthritis etc. as well as cancer and the maladies associated with aging (dementia, Alzheimer's etc.) are on the rise!. Consequently the pharma industry continues to grow and is projected to

achieve sales in excess of trillion dollar mark by 2020 By the next decade, one field which is poised to bring a paradigm change in the way diseases are treated is the Stem cell therapy/Regenerative Medicine space. The number of companies and products in the clinic have reached a critical mass warranting a close watch for those interested in keeping pace with the development of new medicines.

Regenerative Medicine and Stem cell based Cell therapies-Drugs of the Future Offering Hope for Cure

EXECUTIVE SUMMARY

- INTRODUCTION

- Tough Choice- "Autologous vs. Allogenic " Therapies

- REGULATORY GUIDELINES

- Marketed Cell based/Stem Cell Products

- Progress and Challenges

- Progress in Specific Therapy Areas

- SELECT UPCOMING MILESTONES IN REGENERATIVE MEDICINE/STEM

CELL FOCUSED COMPANIES (2015-16)

- Appendix

Read the full report: http://www.reportlinker.com/p02629094-summary/view-report.html

About Reportlinker ReportLinker is an award-winning market research solution that finds, filters and organizes the latest industry data so you get all the market research you need - instantly, in one place.

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To view the original version on PR Newswire, visit:http://www.prnewswire.com/news-releases/regenerative-medicine-and-stem-cell-based-cell-therapies-drugs-of-the-future-offering-hope-for-cure-300153074.html

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Mississippi Stem Cell Treatment Center – Ocean Springs, MS

October 4th, 2015 7:41 pm

As a national pioneer of innovative medicine, Mississippi Stem Cell Treatment Centers motto Excellence with a Human Touch, is at the forefront of what we do. Located in the city of Ocean Springs on the Mississippi Gulf Coast, we provide treatment to promote healing and tissue generation to those suffering from autoimmune, degenerative, inflammatory and ischemic conditions. Our team is highly committed to alleviating your symptoms and enhancing your functionality, quality of life, and wellbeing.

We employ a method called Stromal Vascular Fraction deployment (SVF). SVF relies on individual patient stem cells and growth factors, and helps accelerate healing and tissue regeneration. The SVF we collect from patients fat tissue is given back to the individual through the deployment process. SVF is an innovative product that can be used to regenerate different types of tissue throughout the body.

Mississippi Stem Cell Treatment Center is an affiliate of the Cell Surgical Network of CA. Our center meets all FDA guidelines for treating patients using their own tissue for therapy. We provide same-day harvesting and treatment in a state-of-the-art environment, which facilitates a faster recovery.

We provide treatment for anyone suffering in the following areas:

At Mississippi Stem Cell Treatment Center, we offer stem cell center treatments for autoimmune disease, as well as stem cell center treatment for people suffering from other degenerative diseases. For more information on our innovative technology, browse our website for a wealth of information on stem cells, or contact us so we can discuss your individual candidate profile.

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Arthritis Treatment – 4 Step Arthritis Treatments That Work

October 4th, 2015 10:46 am

The common traditional method that most physicians use is to diagnose and treat the symptoms that are causing you joint pain and inflammation. They use complicated surgeries, joint replacements and strong prescription medications that usually end up causing more pain and suffering that your arthritis! This method has very limited success and has lead to numerous lawsuits from heart attacks and stroke deaths, to name a few, caused by toxic side effects of medications and botched surgeries.

If these actually worked for you or the millions of arthritis sufferers worldwide, you wouldnt be sitting here reading this article. But you know you must do something about this as arthritis, particularly rheumatoid arthritis significantly decreases your lifespan if you do not get effective treatment for it.

Fortunately there is a light at the end of the tunnel here, and it is that you can live a life without arthritis joint pain constantly inhibiting you from doing the things you love without pain and discomfort. If you are serious about leaving your arthritis jailer behind, then you will want to follow this handy guide below for the latest arthritis remedies, treatments and therapies that will stop the endless Inflammation/Swelling/Pain/Immobility cycle of arthritis. Dont go Ballistic go Holistic!

Well, you might ask, just what is this holistic approach? It is not a miracle, its just common sense arthritis treatment thats been overlooked (unfortunately, sometimes on purpose) by those following traditional treatments and still suffering from arthritis pain. This holistic method uses practical knowledge of how a healthy bodys joints operate. What do you think it is in your joints that is causing all this pain, inflammation and swelling? Primarily excess junk calcium (from the wrong type of supplements or processed milk products), heavy metal deposits, and infections that cause your joints to lose their protective cushioning, degenerate and cause terrible pain and unnecessary suffering.

You need to keep your joint moving to keep them flexible and pain free. This is a bit of a conundrum as you may be experiencing too much pain and stiffness to exercise. If this is the case then you should treat the symptoms of arthritis first so you can gain the mobility to exercise and keep your joints moving into permanent recovery from arthritis. Lets look at how we can relieve some of the pressure on the joint socket and the pain its causing so we can begin the healing process.

First you need to stop any infections from happening in your body as this may an underlying cause of arthritis. Then you need to keep your whole body in a more alkaline state and reduce your dietary acid intake. Then you need to rebuild and nourish your joints. Finally you might want to get some natural pain relief until you no longer have this condition. If you have been diagnosed with Autoimmune Arthritis you can also visit the page for Rheumatoid Arthritis for RA specific options.

The 5 step Natural Arthritis Treatment Overview:

1) Treat & Prevent Infections and Detox:

Here is a secret that has been hidden from mainstream medicine but not naturopathic physicians: viruses and pathogens are causing a great deal of arthritis but not even being addressed! Dr. Mark Genovese a top Medical Doctor, Stanford Medicine University Professor and Rheumatologist who is on the leading edge of arthritis and inflammation studies addresses this bluntly:

Theres a perception that arthritis is arthritis, just like some people think cancer is cancer, says Mark Genovese, MD, a rheumatologist and professor at the Stanford School of Medicine. But its just not true. It could be gout, crystals, autoimmune rheumatoid arthritis, virus-caused arthritis or as many as 100 other kinds of the disease.

Since Infection is a root cause of arthritis you need to address it or you will continue with arthritis pain and inflammation indefinitely. Watch this video by Dr. Tent, a Holistic Doctor that explains exactly why you need to treat the viral infections first before you will get lasting arthritis pain relief:

Here is what you will want to do to make sure youve gotten any chronic infections out of your body and particularly joints:

2) Reduce Acid and Alkalize Your Body (Naturally Dissolves Hard Calcium Deposits in Your Body, Brain, Arteries, Kidneys and of course Joints!)

3) Rebuild & Cushion Your Joints Get Pain Relief

If you are suffering with back, neck or hip problems you will want to check out the many great healing products that will make your life much easier. There are:

These devices and techniques can really not only stop but actually heal the source or cause of your arthritis pain. Use the arthritis joint pain remedies to stop the swelling and inflammation, and use the therapies and treatment devices to get your joints healthy and flexible again for pain free joints for life.

Go here to see the original:
Arthritis Treatment - 4 Step Arthritis Treatments That Work

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CDC – Arthritis – Data and Statistics – Cost

October 4th, 2015 10:46 am

National and state cost estimates

Study reports on arthritis costs:

National and state direct and indirect costs are presented in the January 12, 2007 MMWR entitled: National and State Medical Expenditures and Lost Earnings Attributable to Arthritis and Other Rheumatic Conditions United States, 2003.

A detailed report on the national cost study, including the study methods and comparisons of 1997 and 2003 costs, was published in:

Yelin E, Murphy L, Cisternas M, Foreman A, Pasta D, Helmick C. Medical Care Expenditures and Earnings Losses Among Persons with Arthritis and Other Rheumatic Conditions in 2003, and Comparisons to 1997. Arthritis and Rheumatism 2007;56(5):1397-1407.

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Yelin E, Cisternas M, Foreman A, Pasta D, Murphy L, Helmick C. National and state medical expenditures and lost earnings attributable to arthritis and other rheumatic conditions United States, 2003. MMWR 2007;56(1):47. html pdf [306K]

The table below shows the total costs* (in millions of dollars) attributable to arthritis and other rheumatic conditions for each state in 2003.

* Total costs = medical expenditures + lost earnings

Yelin E, Cisternas M, Foreman A, Pasta D, Murphy L, Helmick C. National and state medical expenditures and lost earnings attributable to arthritis and other rheumatic conditions United States, 2003. MMWR 2007;56(1):47. html pdf [306K]

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From 1997 to 2005, total national expenditures among all US adults with arthritis increased from by 100 billion dollars. Medical expenditures were $252.0 billion in 1997 and $353.0 billion in 2005. (Cisternas et al 2009)

Why did total national medical expenditures among all adults with arthritis increase from 1997 to 2005?

Total national medical expenditures among US adults with arthritis, 1997 to 2005

Data source: Medical Expenditure Panel Survey, 1997-2005

Expenditures for each individual are the sum of the following: inpatient, outpatient, office visit, home health, emergency, prescription medications, and other.

The graph above shows that

Cisternas MG, Murphy LB, Yelin EH, Foreman AJ, Pasta DJ, Helmick CG. Trends in Medical Care Expenditures of US Adults with Arthritis and Other Rheumatic Conditions 1997 to 2005 J Rheumatol 2009;36(11):2531-2538. abstract

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Follow this link:
CDC - Arthritis - Data and Statistics - Cost

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