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Muscular Dystrophy

Research Overview

❶In a new study, researchers report they have added new capabilities to an experimental drug agent that previously defeated only one of DM1's many modes of action.

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What is muscular dystrophy?

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Scientists around the globe are conducting intense research to understand what causes muscle dysfunction in Duchenne muscular dystrophy (DMD) and to apply that understanding to the development of effective treatments.

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Current Research The cornerstone of Parent Project Muscular Dystrophy’s mission is to identify and support promising Duchenne muscular dystrophy research that can impact all those living with Duchenne now, during their lifetime. No one in.

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Sep 08,  · Read about the promise of stem cell research for muscular dystrophy patients, and successful treatments tested in dogs. Your source for the latest research news Follow Subscribe. Breaking news in research. from this trial encouraged the Committee for Medicinal Products for Human Use to recommend the expansion of the drug’s current licence to include boys as young as two. (FDA) has granted Orphan Drug Designation to GBC for the treatment of facioscapulohumeral muscular dystrophy.

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Aug 09,  · "Muscular Dystrophy: Hope Through Research", NINDS, Publication date August NIH Publication No. Back to Muscular Dystrophy Information Page See . Cedars-Sinai's muscular dystrophy research is multidisciplinary. Researchers collaborate with the Baloh Laboratory, the Institute of Genetic and Molecular Medicine in the United Kingdom, the University of Florida's Powell Gene Therapy Center, UCLA's Department of Biomathematics and the Center for Duchenne Muscular Dystrophy at UCLA.