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New study sheds light on bone marrow stem cell therapy for pancreatic recovery

Posted: Published on October 3rd, 2012

ScienceDaily (Oct. 2, 2012) Researchers at Cedars-Sinai's Maxine Dunitz Neurosurgical Institute have found that a blood vessel-building gene boosts the ability of human bone marrow stem cells to sustain pancreatic recovery in a laboratory mouse model of insulin-dependent diabetes. The findings, published in a PLoS ONE article of the Public Library of Science, offer new insights on mechanisms involved in regeneration of insulin-producing cells and provide new evidence that a diabetic's own bone marrow one day may be a source of treatment. Scientists began studying bone marrow-derived stem cells for pancreatic regeneration a decade ago. Recent studies involving several pancreas-related genes and delivery methods -- transplantation into the organ or injection into the blood -- have shown that bone marrow stem cell therapy could reverse or improve diabetes in some laboratory mice. But little has been known about how stem cells affect beta cells -- pancreas cells that produce insulin -- or how scientists could promote sustained beta cell renewal and insulin production. When the Cedars-Sinai researchers modified bone marrow stem cells to express a certain gene (vascular endothelial growth factor, or VEGF), pancreatic recovery was sustained as mouse pancreases were able to generate new beta cells. The VEGF-modified stem … Continue reading

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Blind Mice Get Experimental Stem Cell Treatment For Blindness

Posted: Published on October 3rd, 2012

April Flowers for redOrbit.com Your Universe Online Columbia University ophthalmologists and stem cell researchers have developed an experimental treatment for blindness using the patients skin cells, which has improved the vision of blind mice in testing. The findings of this research, published online in the journal Molecular Medicine, suggest that induced pluripotent stem cells (iPS) could soon be used to improve vision in people with macular degeneration and other eye retina diseases. iPS cells are derived from adult human skin cells but have embryonic qualities. With eye diseases, I think were getting close to a scenario where a patients own skin cells are used to replace retina cells destroyed by disease or degeneration, says Stephen Tsang, MD, PhD, associate professor of ophthalmology and pathology & cell biology. Its often said that iPS transplantation will be important in the practice of medicine in some distant future, but our paper suggests the future is almost here. Scientists were very excited by the advent of human iPS cells when they were discovered in 2007, as they provide a way to avoid the ethical complications of embryonic stem cells. Another advantage is that the iPS cells are created from the patients own skin, eliminating … Continue reading

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Blind Mice Get Experimental Stem Cell Treatment For Blindness

Posted: Published on October 3rd, 2012

April Flowers for redOrbit.com Your Universe Online Columbia University ophthalmologists and stem cell researchers have developed an experimental treatment for blindness using the patients skin cells, which has improved the vision of blind mice in testing. The findings of this research, published online in the journal Molecular Medicine, suggest that induced pluripotent stem cells (iPS) could soon be used to improve vision in people with macular degeneration and other eye retina diseases. iPS cells are derived from adult human skin cells but have embryonic qualities. With eye diseases, I think were getting close to a scenario where a patients own skin cells are used to replace retina cells destroyed by disease or degeneration, says Stephen Tsang, MD, PhD, associate professor of ophthalmology and pathology & cell biology. Its often said that iPS transplantation will be important in the practice of medicine in some distant future, but our paper suggests the future is almost here. Scientists were very excited by the advent of human iPS cells when they were discovered in 2007, as they provide a way to avoid the ethical complications of embryonic stem cells. Another advantage is that the iPS cells are created from the patients own skin, eliminating … Continue reading

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Cedars-Sinai study sheds light on bone marrow stem cell therapy for pancreatic recovery

Posted: Published on October 3rd, 2012

Public release date: 2-Oct-2012 [ | E-mail | Share ] Contact: Sandy Van sandy@prpacific.com 808-526-1708 Cedars-Sinai Medical Center LOS ANGELES (Oct. 2, 2012) Researchers at Cedars-Sinai's Maxine Dunitz Neurosurgical Institute have found that a blood vessel-building gene boosts the ability of human bone marrow stem cells to sustain pancreatic recovery in a laboratory mouse model of insulin-dependent diabetes. The findings, published in a PLOS ONE article of the Public Library of Science, offer new insights on mechanisms involved in regeneration of insulin-producing cells and provide new evidence that a diabetic's own bone marrow one day may be a source of treatment. Scientists began studying bone marrow-derived stem cells for pancreatic regeneration a decade ago. Recent studies involving several pancreas-related genes and delivery methods transplantation into the organ or injection into the blood have shown that bone marrow stem cell therapy could reverse or improve diabetes in some laboratory mice. But little has been known about how stem cells affect beta cells pancreas cells that produce insulin or how scientists could promote sustained beta cell renewal and insulin production. When the Cedars-Sinai researchers modified bone marrow stem cells to express a certain gene (vascular endothelial growth factor, or VEGF), pancreatic recovery … Continue reading

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FDA Approves Stemedica Phase II Clinical Trial for Acute Myocardial Infarction With Ischemia Tolerant Mesenchymal Stem …

Posted: Published on October 3rd, 2012

SAN DIEGO, Calif., Oct. 2, 2012 (GLOBE NEWSWIRE) -- via PRWEB - Stemedica Cell Technologies, Inc., a leader in adult allogeneic stem cell manufacturing, research and development, announced today that the U.S. Food and Drug Administration (FDA) approved its application for an Investigational New Drug (IND) to assess the clinical effects of Stemedyne-MSC (Stemedica's human bone marrow-derived ischemia tolerant mesenchymal cells) in subjects with a myocardial infarct. The Phase IIa double-blinded randomized clinical trial will study approximately forty (40) patients. All patients will initially receive standard care including percutaneous transluminal coronary angioplasty (PTCA) and stenting and, upon completion, will be randomized to receive Stemedyne-MSC intravenously or placebo. The clinical trial will address the prevalence of cardiovascular disease estimated to carry a global disease burden in excess of $400 billion each year. More than one million patients undergo PTCA and stenting in the Untied States annually; another 800,000 have the procedures each year in Europe. Nabil Dib, M.D., MSc., F.A.C.C., Director of Cardiovascular Research at Mercy Gilbert and Chandler Regional Medical Centers, and an Associate Professor of Medicine and Director of Clinical Cardiovascular Cell Therapy at the University of California, San Diego, will serve as the principal investigator of the FDA-approved … Continue reading

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Celebrities and Rare Disease Community Turn Out To Support Global Genes Project's 1st Annual "Tribute to Champions of …

Posted: Published on October 2nd, 2012

Rare Disease Industry Leaders and Advocates Honored; Recording Artists Chris Mann, Katrina Parker and Elliott Yamin Gave Touching Performances DANA POINT, Calif., Oct.2, 2012 /PRNewswire-USNewswire/ --On September 27, 2012, rare disease patients, advocates, patient organizations, government agencies, pharmaceutical companies, medical researchers, celebrities, Olympic champions and private sector representatives attended the Global Genes | R.A.R.E. Project (www.globalgenes.org) 1st Annual "RARE Tribute to Champions of Hope" benefit at the Balboa Bay Club & Resort in Newport Beach, CA. The evening was a star-studded affair to raise funds and awareness for rare and genetic diseases that impact 1 in 10 Americans and 350 million people globally. More than 400 guests attended the benefit and a number of awards were presented to celebrate the pioneering achievements of individuals and organizations championing the rare and genetic disease cause. "It was such an honor to celebrate the accomplishments of these remarkable rare disease award recipients," Nicole Boice, president of the Global Genes Project. "We are also incredibly grateful to the artists and stars who volunteered their time and talent to make our first event a tremendous success. Their support means the world to the millions of rare disease patients who know they are not alone in … Continue reading

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Sarepta Therapeutics Announces Conference Call and Webcast on Wednesday, October 3, 2012, to Discuss 48-Week Results …

Posted: Published on October 2nd, 2012

SOURCE: Sarepta Therapeutics, Inc. CAMBRIDGE, MA--(Marketwire - Oct 2, 2012) - Sarepta Therapeutics, Inc. (NASDAQ: SRPT), a developer of innovative RNA-based therapeutics, announced today it will hold a conference call at 8:00 a.m. EDT (5:00 a.m. PDT) on Wednesday, October 3, 2012 to discuss 48-week results from its Phase IIb study evaluating eteplirsen for the treatment of Duchenne muscular dystrophy (DMD). The conference call may be accessed by dialing 866.356.3093 for domestic callers and 617.597.5381 for international callers. The passcode for the call is 93880948. Please specify to the operator that you would like to join the "Sarepta Therapeutics 48-Week Results Call."The conference call will be webcast live under the events section of Sarepta's website at http://www.sareptatherapeutics.com and will be archived there following the call for 90 days. Please connect to Sarepta's website several minutes prior to the start of the broadcast to ensure adequate time for any software download that may be necessary. About Sarepta Therapeutics Sarepta Therapeutics is focused on developing first-in-class RNA-based therapeutics to improve and save the lives of people affected by serious and life-threatening rare and infectious diseases. The Company's diverse pipeline includes its lead program eteplirsen, for Duchenne muscular dystrophy, as well as potential … Continue reading

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RI Hospital: Differences in diagnosis, treatment of nonepileptic seizures in US, Chile

Posted: Published on October 2nd, 2012

Public release date: 2-Oct-2012 [ | E-mail | Share ] Contact: Ellen Slingsby eslingsby@lifespan.org 401-444-6421 Lifespan PROVIDENCE, R.I. Epileptic and psychogenic nonepileptic seizures (PNES) may look similar, but actually have different causes and treatments. Up to 20 percent of patients diagnosed with epilepsy actually have PNES, which are not treated by antiepileptic drugs (AEDs). According to a new study by Rhode Island Hospital researcher W. Curt LaFrance Jr., M.D., M.P.H., director of neuropsychiatry and behavioral neurology, increasing access to video electroencephalography (video-EEG) may aid in distinguishing between epilepsy and PNES. The study is published online in advance of print in the journal Epilepsy & Behavior. This is the first study to compare how clinicians diagnose and treat PNES in a North American country and a South American country, and underscores the importance of access to video-EEG to conclusively make the diagnosis of PNES. It compared diagnosis and treatment practices among clinicians in the U.S. and Chile who treat epilepsy and PNES to assess standard medical care for PNES. In the U.S., 89 percent of clinician respondents reported using inpatient video-EEG to diagnosis PNES, which is the gold standard for diagnosis. However, this diagnostic tool is not always available in other … Continue reading

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New Studies on Zebinix® Presented at Leading European Epilepsy Congress

Posted: Published on October 2nd, 2012

HATFIELD, England, October 3, 2012 /PRNewswire/ -- Bial and Eisai today present information on new studies designed to increase the understanding of the use of Zebinix(R) (eslicarbazepine acetate), a once-daily adjunctive therapy for adults with partial-onset seizures, with or without secondary generalisation, at the 10th European Congress on Epileptology (ECE) in London.[1] These new data will be important as the successful treatment of partial-onset seizures remains a challenge, and up to a third of people with epilepsy do not achieve freedom from seizures despite appropriate therapy with anti-epileptic drugs.[2] Eslicarbazepine acetate in Partial-Onset Seizures study (EPOS)[3] Launched in March 2012, the Eslicarbazepine acetate in Partial-Onset Seizures (EPOS) study design presented here aims to provide a better understanding of the use of eslicarbazepine acetate in a clinical practice setting. EPOS is a prospective, multicentre, open-label, non-interventional study of adults with partial-onset seizures insufficiently controlled by monotherapy anti-epileptic treatment. The goal is to recruit approximately 800 patients from over 200 centres in Denmark, France, Germany, Norway, Sweden and the UK. The study primary endpoint will be 6-month retention rate and other assessments will include seizure frequency, adverse events and quality of life. "The significant number of people with epilepsy who fail to … Continue reading

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Epilepsy Burdens Developing Countries

Posted: Published on October 2nd, 2012

Developing countries are seeing rising rates of noncommunicable diseases such as diabetes, cancer and cardiovascular disease. But researchers say those countries already have a disproportionate number of epilepsy cases compared to richer nations. Researchers say despite epilepsy being one of the most cost-effective disorders to treat, developing nations carry a heavy burden. Twice as many people with epilepsy live in low and middle income countries. The findings appear in The Lancet medical journal. Oxford University Psychiatry Professor Charles Newton is the lead author. He spends much of his time in Kenya and Tanzania in the Wellcome Trust programs. Epilepsy is a condition in which there is an excessive neuronal or electrical discharge within the brain causing the person to develop abnormal movements or impaired consciousness or even in some cases abnormal sensations, he said. Epilepsy is an umbrella term for a condition that has many causes and can happen at any age. It can be inherited. It can have other genetic causes. It can be cause by infections, birth trauma, head injury and even such things as stroke and brain tumors, he said. Newton said that in Africa birth trauma often results from poor obstetrical care. And brain infections can … Continue reading

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