This Month in Muscular Dystrop

Hosted by Kevin Flanigan, MD, "This Month in Muscular Dystrophy" podcasts highlight the latest in muscular dystrophy and other inherited neuromuscular disease research. During each podcast, authors of recent publications discuss how their work improves our understanding of inherited neuromuscular diseases, and what their work might mean for treatment of these diseases.

This Month in Muscular Dystrop

All Tracks from This Month in Muscular Dystrop

Dr. Jerry Mendell Discusses Phase 1/2a Follistatin Gene Therapy Trial for Becker Muscular Dystrophy

Dr. Kevin Flanigan Discusses IRES-Induced Dystrophin as a Potential Therapy for DMD

Dr. Louise Rodino-Klapac Discusses Dysferlin Overlap Vectors to Restore Function in Dysferlinopathie

Dr. Scott Harper Discusses RNAi silencing in Limb Girdle Muscular Dystrophy 1A

Dr. Brian Kaspar Discusses a New Method for Studying ALS, with Potential to Test Therapeutics in Ind

Dr. Louis Chicoine Discusses the Effect of Plasmapheresis in Removal of AAV Antibodies for Gene Ther

Dr. Volker Straub Discusses the Use of Muscle MRI in Muscular Dystrophy

Dr. Jeff Chamberlain Discusses Gene and Cell Mediated Therapies for Muscular Dystrophy

Dr. Paul Martin Discusses Galgt2 Gene Therapy for Muscular Dystrophy

Dr. Louise Rodino-Klapac Discusses Alpha 7 Integrin As A Therapeutic Approach to Muscular Dystrophy

Dr. James Ervasti Discusses Stability of Therapeutic Forms of Dystrophin :: January 2013

Dr. Federica Montanaro Discusses New Cardiac Dystrophin Associated Proteins

Professor Francesco Muntoni Discusses Congenital Muscular Dystrophies

Dr. Louise Rodino-Klapac Discusses Advances in Dysferlin Gene Therapy

Dr. Hugh Allen Discusses Cardiomyopathy in Duchenne Muscular Dystrophy

Dr. Jerry Mendell Discusses Newborn Screening in Duchenne Muscular Dystrophy

Dr. Thomas Voit Discusses Gamma Sarcoglycan Gene Therapy

Dr. Burghes Discusses Antisense Oligomer Treatment in an SMA Mouse Model

Dr. Steve Wilton Discusses Antisense-Induced Exon Skipping

Dr. Scott Harper Discusses DUX4 as a Potential Candidate Gene for Facioscapulohumeral Muscular Dystr