Spinal muscular atrophy - Lenox Hill Hospital
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Spinal muscular atrophy - Lenox Hill Hospital
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Tags: Muscle, Hospital, Hospitals
Most Recently Shared on August 9, 2010 at 8:57 pm By:
It’s Spinal Muscle Atrophy Awareness Month. To learn about spinal muscle atrophy visit: http://cot.ag/cpTfUh
Neuromuscular Clinic | Muscular Dystrophy | MDA | Services | Clinical Trials - Childrens Hospital Los Angeles
chla.org — “The Muscular Dystrophy Association (MDA) Children's Hospital Los Angeles Neuromuscular Clinic provides care for children with muscular dystrophy, spinal muscular atrophy, Charcot-Marie-Tooth disease and other muscular diseases.” View full resource at chla.org
Most Recently Shared on March 13, 2012 at 7:14 pm By:
Learn about the new Neuromuscular Clinic @ChildrensLA and our partnership with @MDALosAngeles #kids #health http://t.co/DrDwSGkD
Failure in nerve-fiber navigation corrected in zebrafish model, suggests possibility of drug treatment
medicalxpress.com — “Spinal muscular atrophy (SMA) is the leading genetic cause of death in children under 2, with no treatment other than supportive care. In the Proceedings of the National Academy of Sciences, researchers at Children's Hospital Boston show how loss or mutation of the SMA gene causes progressive muscle ...” View full resource at medicalxpress.com
Most Recently Shared on June 6, 2011 at 7:00 pm By:
Failure in nerve-fiber navigation corrected in zebrafish model, suggests possibility of drug treatment http://tw.medicalxpress.com/226576963
Spinal Muscular Atrophy Research Team Receives Pepsi Refresh Funds From Sophia's Cure Foundation
medicalnewstoday.com — “Brian Kaspar, PhD, principal investigator in the Center for Gene Therapy at The Research Institute at Nationwide Children's Hospital, along with a team of Spinal Muscular Atrophy (SMA) researchers” View full resource at medicalnewstoday.com
Most Recently Shared on September 9, 2010 at 10:00 pm By:
Spinal Muscular Atrophy Research Team Receives Pepsi Refresh Funds From Sophia's Cure Foundation http://mnt.to/3Jwm #genetics
Spinal Muscular Atrophy Research Team Receives Pepsi Refresh Funds from Sophia's Cure Foundation
newswise.com — “Brian Kaspar, PhD, principal investigator in the Center for Gene Therapy at The Research Institute at Nationwide Children's Hospital, along with a team of Spinal Muscular Atrophy (SMA) researchers and clinicians, recently received a $250,000 grant for SMA research and clinic development from Sophia's Cure Foundation via the Pepsi Refresh Project.” View full resource at newswise.com
Most Recently Shared on September 8, 2010 at 3:41 pm By:
Spinal Muscular Atrophy Research Team Receives Pepsi Refresh Funds from Sophia's Cure Foundation: Brian Kaspar, Ph... http://bit.ly/bELvTc
Spinal Muscular Atrophy May Also Affect the Heart
newswise.com — “Along with skeletal muscles, it may be important to monitor heart function in patients with spinal muscular atrophy (SMA). These are the findings from a study conducted by Nationwide Children's Hospital and published online ahead of print in Human Molecular Genetics. This is the first study to report cardiac dysfunction in mouse models of SMA.” View full resource at newswise.com
Most Recently Shared on August 11, 2010 at 12:36 pm By:
Spinal Muscular Atrophy May Also Affect the Heart: Along with skeletal muscles, it may be important to monitor hea... http://bit.ly/aQuNI8
Spinal muscular atrophy may lead to cardiac dysfunction: Study
news-medical.net — “Along with skeletal muscles, it may be important to monitor heart function in patients with spinal muscular atrophy (SMA). These are the findings from a study conducted by Nationwide Children's Hospital and published online ahead of print in Human Molecular Genetics. This is the first study to report cardiac dysfunction in mouse models of SMA.” View full resource at news-medical.net
Most Recently Shared on August 11, 2010 at 10:52 am By:
Genetics News: Spinal muscular atrophy may lead to cardiac dysfunction: Study: Along with skeletal muscles, it may... http://bit.ly/bgwYdJ
Events, SMA Education Day: Clinical Updates for Parents of Children with Spinal Muscular Atrophy, UW Health, University of Wisconsin Hospital and Clinics, UW Physician, Madison, UW Health, University of Wisconsin Hospital, Madison
uwhealth.org — “Events, SMA Education Day: Clinical Updates for Parents of Children with Spinal Muscular Atrophy, UW Health, University of Wisconsin Hospital and Clinics, UW Physician, Madison, UW Health, University of Wisconsin Hospital, Madison” View full resource at uwhealth.org
Most Recently Shared on July 26, 2010 at 3:30 pm By:
Parents of children with Spinal Muscular Atrophy: Get the latest clinical updates Aug. 14. Registration deadline Friday. http://ow.ly/2gEVy
Opening New Avenue For Developing Treatments For Genetic Muscle-Wasting Disease
medicalnewstoday.com — “Scientists from the Ottawa Hospital Research Institute (OHRI) and the University of Ottawa have identified a promising new approach for developing drugs to treat Spinal muscular atrophy (SMA), the” View full resource at medicalnewstoday.com
Most Recently Shared on March 17, 2010 at 1:21 pm By:
Opening New Avenue For Developing Treatments For Genetic Muscle-Wasting Disease http://mnt.to/3z29 #genetics
Blocking RhoA enzyme increases survival in SMA mouse model
buzzup.com — “Scientists from the Ottawa Hospital Research Institute (OHRI) and the University of Ottawa have identified a promising new approach for developing drugs to treat Spinal muscular atrophy (SMA), the leading inherited cause of death in infants and toddlers. Dr. Rashmi Kothary and his doctoral student Melissa Bowerman have found that an enzyme called RhoA is overly active in a mouse model of the disease and blocking this enzyme can greatly increase survival. The study is published in Human Molecular” View full resource at buzzup.com
Most Recently Shared on March 16, 2010 at 6:18 pm By:
Genetics News: Blocking RhoA enzyme increases survival in SMA mouse model: Scientists from the Ottawa Hospital R... http://buzzup.com/qkcz
Study opens new avenue for developing treatments for genetic muscle-wasting disease
physorg.com — “Scientists from the Ottawa Hospital Research Institute (OHRI) and the University of Ottawa have identified a promising new approach for developing drugs to treat Spinal muscular atrophy (SMA), the leading inherited cause of death in infants and toddlers. Dr. Rashmi Kothary and his doctoral student Melissa ...” View full resource at physorg.com
Most Recently Shared on March 15, 2010 at 2:49 pm By:
Study opens new avenue for developing treatments for genetic muscle-wasting disease http://tw.physorg.com/187868935
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