Critical Research Initiatives in Duchenne Muscular Dystrophy

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Critical Research Initiatives in Duchenne Muscular Dystrophy

disabled-world.com

Duchenne the most common form of childhood muscular dystrophy is a progressive and fatal muscle disorder affecting boys and young men

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Tags: Genetic, Muscular Dystrophy, Muscle, Disease and Condition, Children's Health, Men's Health

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Most Recently Shared on June 10, 2010 at 3:32 pm By:

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Critical Research Initiatives in Duchenne Muscular Dystrophy http://ff.im/-lO55H

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AVI BioPharma, MDA to initiate exon-51 Phase 2 trial in Duchenne muscular dystrophy

news-medical.net — “More than a decade of targeted Muscular Dystrophy Association-funded research, made possible as a result of generous public support of the MDA Labor Day Telethon and thousands of grass-roots special events, has today culminated in MDA providing financial assistance for the start of the first Phase 2 placebo-controlled, multiple dose efficacy, safety, tolerability and pharmacokinetics clinical trial of an exon-51 skipping drug, eteplirsen, as a potential therapy for Duchenne muscular dystrophy.View full resource at news-medical.net

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Most Recently Shared on August 16, 2011 at 5:33 am By:

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AVI BioPharma, MDA to initiate exon-51 Phase 2 trial in Duchenne muscular dystrophy: More than a decade of targe... http://t.co/YLZCnEw

10 months ago...

Drug Screen Points The Way To Potential New Duchenne Muscular Dystrophy Treatments - QualityPoint Technologies

qualitypointtech.net — “Armed with a zebrafish model of Duchenne muscular dystrophy (DMD) and a library of 1,200 chemicals already approved for human use, researchers at Children's Hospital Boston have identified a compound that reverses the loss of muscle structure and function associated with DMD, seemingly by compensating for the loss of a critical protein. The discovery, published on March 14 in the online Early Edition of the Proceedings of the National Academy of Sciences (PNAS), opens up new avenues for understaView full resource at qualitypointtech.net

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Most Recently Shared on March 20, 2011 at 8:00 am By:

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Drug Screen Points The Way To Potential New Duchenne Muscular Dystrophy Treatments: Armed with a zebrafish model o... http://bit.ly/e4qCLF

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