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Related to Duchenne muscular dystrophy: Becker muscular dystrophy
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References in periodicals archive ?
The company hopes to meet with the FDA to discuss the CAP-1002 development program for treatment of Duchenne muscular dystrophy, and specifically the HOPE-2 Trial.
Duchenne muscular dystrophy is a devastating genetic disorder that causes muscle degeneration and leads to death, generally before the age of 30, most commonly from heart failure.
Orofacial dysfunction in Duchenne muscular dystrophy.
The report reviews key players involved Duchenne Muscular Dystrophy therapeutics and enlists all their major and minor projects
The mission of New York-based Michael's Cause is to raise awareness of Duchenne muscular dystrophy as well as direct funding for research by building a strong foundation for future treatments and a possible cure.
Treatments for Duchenne muscular dystrophy are limited to steroids and physical therapy that slow disease progression and lessen symptoms.
Selective deficits in verbal working memory associated with a known genetic etiology: the neuropsychological profile of duchenne muscular dystrophy.
The pioneering drug is the first ever to tackle the causes of Duchenne muscular dystrophy.
After laboratory mice with Duchenne muscular dystrophy were infused with cardiac stem cells, the mice showed steady, marked improvement in heart function and increased exercise capacity.
Duchenne Muscular Dystrophy is one of the most common fatal genetic disorders to affect children around the world.
Duchenne muscular dystrophy (DMD) is a fatal neuromuscular disease, affecting 1:3500 live male births [1].