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New York Genome Center announces the New York Stem Cell Foundation as an Associate Member

Posted: Published on September 17th, 2013

Public release date: 17-Sep-2013 [ | E-mail | Share ] Contact: David McKeon dmckeon@nyscf.org 212-365-7440 New York Stem Cell Foundation New York, NY (September 17, 2013) The New York Genome Center (NYGC) announced today that The New York Stem Cell Foundation (NYSCF) has become an Associate Member, joining NYGC's growing consortium of 16 research and clinical institutions, all working together in new ways to utilize genomic data for better detection, treatment, and prevention of disease. "Biologists at the NYSCF working with the genomic scientists at NYGC will help address some of the critical roadblocks in stem cell research," said Dr. Robert B. Darnell, President and Scientific Director of NYGC. "Modern genomics has the potential to provide vital missing information to help us learn how to harness stem cells for use in clinical medicine. We've developed techniques and ideas here at NYGC that will greatly synergize with the beautiful and pioneering work ongoing at the NYSCF." Stem cell biology and genomic analysis are both critical to the advancement of precision medicine. The collaboration between the Genome Center and NYSCF will merge cutting-edge capabilities in human biology with genomic research, creating an optimal environment for translating research into a better standard of … Continue reading

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Stem Cell Therapeutics Adopts Shareholder Rights Plan

Posted: Published on September 17th, 2013

TORONTO, ONTARIO--(Marketwired - Sep 17, 2013) - Stem Cell Therapeutics Corp. (TSX VENTURE:SSS)(SCTPF), a biopharmaceutical company developing cancer stem cell-related therapeutics, today announces that it has adopted a shareholder rights plan (the "Plan") effective September 16, 2013. The Company will be seeking shareholder approval of the Plan at its next annual general and special meeting of shareholders. The Plan is designed to ensure the fair and equal treatment of shareholders in connection with any take-over bid for outstanding common shares of the Company. The Plan is not intended to prevent or deter take-over bids that offer fair treatment and value to shareholders, but is designed to encourage offers that represent fair value to all shareholders. The Plan seeks to provide shareholders with adequate time to properly assess a take-over bid without undue pressure. It also provides the Board of Directors with adequate time to fully assess an unsolicited take-over bid, to allow competing bids to emerge, and, if applicable, to explore other alternatives to the take-over bid to maximize shareholder value. Under the terms of the Plan, one right will be issued by the Company for each outstanding Stem Cell Therapeutics ("SCT") common share at the close of business on … Continue reading

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New muscular dystrophy treatment shows promise in early study led by Children's National

Posted: Published on September 17th, 2013

Public release date: 17-Sep-2013 [ | E-mail | Share ] Contact: Emily Hartman ehartman@childrensnational.org 202-476-4500 Children's National Medical Center WASHINGTON, DC A preclinical study led by researchers at Children's National Medical Center has found that a new oral drug shows early promise for the treatment of Duchenne muscular dystrophy (DMD). The results, published in EMBO Molecular Medicine, show that the drug, VBP15, decreases inflammation and protects and strengthens muscle without the harsh side effects linked to current treatments with glucocorticoids such as prednisone. Duchenne muscular dystrophy results in severe muscle degeneration and affects approximately 180,000 patients worldwide, mostly children. The current standard treatment uses glucocorticoids, but is limited due to serious side effects leading to fragile bones and suppression of both the immune system and growth. "These findings, while preliminary, are very promising for advancing the treatment of this disease, which causes disability in so many children worldwide," said Eric P. Hoffman, PhD, director of the Center for Genetic Medicine Research at Children's National. "The study also suggests the potential for new strategies in very early treatment, which could further benefit patients." The Children's National research team also observed that VBP15 inhibits the transcription factor NF-B, a key cell-signaling molecule … Continue reading

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Treatment options for epilepsy – Video

Posted: Published on September 17th, 2013

Treatment options for epilepsy Jehuda Sepkuty, M.D., Medical Director of the Epilepsy Center and Clinical Neurophysiology Program at the Swedish Neuroscience Institute, talks about diagnos... By: swedishseattle … Continue reading

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Sunovion Reports Eslicarbazepine Acetate Meets Primary Endpoint in Two Phase 3 Monotherapy Studies for Partial-onset …

Posted: Published on September 17th, 2013

MARLBOROUGH, Mass.--(BUSINESS WIRE)-- Sunovion Pharmaceuticals Inc. (Sunovion) today announced that two completed Phase 3 trials of eslicarbazepine acetate (ESL) as a monotherapy treatment (Studies 093-045 and 093-046) met their primary endpoint. ESL was well-tolerated and demonstrated seizure control rates superior to historical controls in adult patients with partial-onset seizures with or without secondary generalization who were not well-controlled by current antiepileptic drugs (AEDs). ESL is an investigational AED currently under review by the U.S. Food and Drug Administration (FDA) for use as a once-daily adjunctive therapy in the treatment of partial-onset seizures in patients 18 years and older with epilepsy. The efficacy and safety of ESL as an adjunctive or monotherapy treatment for partial-onset seizures in adults living with epilepsy has not yet been established. We are pleased to achieve this important milestone in monotherapy, which builds upon our existing data in adjunctive therapy for patients suffering from partial-onset seizures, said Fred Grossman, D.O., FAPA, Senior Vice President, Clinical Development and Medical Affairs at Sunovion. Pending the outcome of FDA review of the current New Drug Application (NDA) resubmission for eslicarbazepine acetate as an adjunctive treatment, Sunovion plans to submit these data as part of a supplemental NDA in support … Continue reading

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Spectacular Bond: Reaching the Child with Autism

Posted: Published on September 17th, 2013

SAN DIEGO--(BUSINESS WIRE)-- As the number of children diagnosed with autism has skyrocketed, thousands of families face daily challenges with unpredictable outbursts, aggressive behaviors, compulsions, and withdrawal from contact. In the new book Spectacular Bond: Reaching the Child with Autism, two doctors from Columbia University and a parent of a child with autism present a life-changing autism treatment program that leads to major improvements in behavior, communication, and social interaction. The program Spectacular Bond takes aspects of the parent-child relationship that typically run on auto-pilot and brings these intricacies into consciousness. Conscious control over these subtle and typically hidden aspects of the parent-child relationship enables parents to confidently handle the range of challenging behaviors they encounter. The book details a six-component plan that, within weeks, leads to The end result is a transformation in the life of the child, the parent, and all members of the family. Spectacular Bond is the only autism behavior program that combines the latest research in neuroscience, linguistics, and the psychology of parent-child interaction. In a field where meaningful progress is thought to take years to achieve, this book shakes conventional wisdom. The program diverges from current mainstream treatment models. Most parents of children with … Continue reading

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'Beauty rest' effect of CPAP sleep apnea treatment

Posted: Published on September 17th, 2013

Featured Article Academic Journal Main Category: Sleep / Sleep Disorders / Insomnia Also Included In: Cardiovascular / Cardiology Article Date: 16 Sep 2013 - 8:00 PDT Current ratings for: 'Beauty rest' effect of CPAP sleep apnea treatment 5 (2 votes) 5 (1 votes) Getting a good night's rest can improve our health in many ways. And now, a new study published in the Journal of Clinical Sleep Medicine is the first of its kind to analyze how patients appear more alert, youthful and attractive after undergoing sleep apnea treatment for 2 months. The treatment, called continuous positive airway pressure (CPAP) therapy, can stop snoring, improve alertness and reduce blood pressure by keeping the airway open through a stream of air delivered by a mask that is worn during sleep. It helps patients with obstructive sleep apnea (OSA), which researchers say is a sleep illness that is linked to an increased risk of high blood pressure, heart disease, diabetes, depression and stroke. However, for some patients, sticking with the CPAP treatment can be a challenge because they must wear the breathing mask all through the night. After anecdotal stories about how patients appeared to look better after consistently following CPAP treatment, … Continue reading

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InVivo Therapeutics Appoints Gregory D. Perry as Interim CFO

Posted: Published on September 17th, 2013

CAMBRIDGE, Mass.--(BUSINESS WIRE)-- InVivo Therapeutics Holdings Corp. (NVIV), a drug delivery company with a focus on groundbreaking technologies for thetreatment of spinal cord injuries(SCI) and neurotrauma conditions, today announced that Gregory D. Perry has been appointed as interim CFO, commencing September 23, 2013. Mr. Perry was most recently the Executive Vice President and CFO of Immunogen, Inc. Prior to joining Immunogen, Mr. Perry served as CFO of Elixir Pharmaceuticals, Inc. from 2007 to 2009. Prior to Elixir, he was CFO of Domantis Ltd., which was acquired by GlaxoSmithKline in 2006. Previously, Mr. Perry was Senior Vice President and CFO of Transkaryotic Therapies, Inc. until its acquisition by Shire plc in 2005. Mr. Perry is currently a member of the Board of Directors of Advanced Cell Technology, Inc. "We are excited tobring on boarda CFO with the integrity, talent and experience of Greg Perry, said Mike Astrue, the interim CEO of InVivo. "His breadth of experience can add value to InVivo in a variety of ways." About InVivo Therapeutics InVivo Therapeutics Holdings Corp. is focused on utilizing polymers as a platform technology to develop treatments for serious diseases and conditions, including improving function in individuals paralyzed as a result of traumatic … Continue reading

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Parkinson's symposium honors doctor who developed deep brain stimulation treatment

Posted: Published on September 17th, 2013

GRAND RAPIDS, MI A doctor who developed deep brain stimulation treatment will be honored at the second annual Grand Challenges in Parkinson's Disease symposium at Van Andel Institute. The event, which will be held Wednesday and Thursday, Sept. 18-19, is open to Parkinson's patients and caregivers as well as scientists. It brings together global leaders in Parkinson's and neurodegenerative disease research. Dr. Alim Louis Benabid, a French neurologist and researcher, will receive the Jay Van Andel Award for Outstanding Achievement in Parkinson's Disease Research. He will give a lecture at 9:15 a.m. Wednesday. Dr. Benabid has made an incredible contribution to the treatment of Parkinson's disease by developing deep brain stimulation," said Dr. Patrik Brundin, head of the translational Parkinson's disease laboratory at the Van Andel Institute. "Today over 140,000 advanced Parkinsons patients have undergone DBS treatment, which essentially changes the 'electric connections' in the brain, and they are able to move remarkably much better thanks to Dr. Benabid's invention." Benabid's work is credited with helping more than 140,000 people seeking help coping with Parkinson's disease. Benabid, the chairman of the board of the Clinatec Institute in Grenoble, France, recently received the 2013 Robert H. Pritzker Prize for Leadership from … Continue reading

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Mum seeks fundraising help to give son a chance to walk

Posted: Published on September 17th, 2013

Mum seeks fundraising help to give son a chance to walk 6:00pm Tuesday 17th September 2013 in News A MOTHER is trying to raise 15,000 to send her disabled son to receive treatment that could enable him to walk. Camren Haines, three, has a form of cerebral palsy that means he cannot stand and can move only by pulling himself along by his arms. Mum Sophie Haines, 27, of Kidlington, hopes to send him to The Footsteps Centre in Dorchester-on-Thames. The centre offers specialist rehabilitation that will help strengthen Camrens muscles and could help him to crawl or walk in the future. Mrs Haines said: I cannot put into words how happy it would make me feel to see him stand up and walk for himself. Just to see him do something for himself, something most children do without a second thought, would make the last three years a little bit less painful. Camren was born prematurely at 27 weeks and was rushed to the Special Care Baby Unit (SCBU) at the John Radcliffe Hospital in Oxford. When he was discharged 111 days later, said Mrs Haines, she was told he was fine, but she found he could not extend … Continue reading

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