Pathophysiology of Duchenne Muscular Dystrophy: Current Hypotheses
Top Cited Papers
- 1 January 2007
- journal article
- review article
- Published by Elsevier in Pediatric Neurology
- Vol. 36 (1) , 1-7
- https://doi.org/10.1016/j.pediatrneurol.2006.09.016
Abstract
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This publication has 70 references indexed in Scilit:
- Oxandrolone enhances skeletal muscle myosin synthesis and alters global gene expression profile in Duchenne muscular dystrophyAmerican Journal of Physiology-Endocrinology and Metabolism, 2006
- Human muscle gene expression responses to endurance training provide a novel perspective on Duchenne muscular dystrophyThe FASEB Journal, 2005
- Loss of sarcolemma nNOS in sarcoglycan‐deficient muscleThe FASEB Journal, 2002
- Long‐term study of Ca2+ homeostasis and of survival in collagenase‐isolated muscle fibres from normal and mdx miceThe Journal of Physiology, 2002
- Helper (CD4+) and Cytotoxic (CD8+) T Cells Promote the Pathology of Dystrophin-Deficient MuscleClinical Immunology, 2001
- Calpain: A Protease in Search of a Function?Biochemical and Biophysical Research Communications, 1998
- Prevention of myonecrosis in mdx mice: Effect of immobilization by the local tetanus methodBrain & Development, 1992
- Costameres are sites of force transmission to the substratum in adult rat cardiomyocytes.The Journal of cell biology, 1992
- Small‐caliber skeletal muscle fibers do not suffer necrosis in mdx mouse dystrophyMuscle & Nerve, 1988
- A double-blind placebo controlled trial of diltiazem in duchenne dystrophyJournal of Molecular Medicine, 1988