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Duchenne Muscular Dystrophy -- See Muscular Dystrophy, Duchenne


An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415)
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2 Duchenne muscular dystrophy.   7
3 Duchenne muscular dystrophy -- History. : The history of a genetic disease : Duchenne muscular dystrophy or Meryon's disease / Alan E. H. Emery & Marcia L. H. Emery  1995 1
4 Duchenne muscular dystrophy -- Laboratory manuals : Duchenne muscular dystrophy : methods and protocols / edited by Camilla Bernardini  2018 1
5 Duchenne muscular dystrophy -- Patients.   2
6 Duchenne muscular dystrophy -- Patients -- Rehabilitation.   2
7 Duchenne muscular dystrophy -- Treatment   4
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