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Neuromuscular Disorders : NMD|July 24, 2012
Cell models for McArdle disease and aminoglycoside-induced read-through of a premature termination codonKathryn E Birch, Ros M Quinlivan, Glenn E MorrisBMJ Case Reports|October 9, 2014
Emotionally-intense situations can result in rhabdomyolysis in McArdle diseaseStefen Brady, Richard Godfrey, Renata S Scalco, et al.Journal of Sports Sciences|April 16, 2014
Heart rate and perceived muscle pain responses to a functional walking test in McArdle diseaseJohn P Buckley, Ros M Quinlivan, Julius Sim, et al.Clinical and Experimental Rheumatology|March 2, 2023
Two emerging phenotypes of atypical inclusion body myositis: illustrative casesSharfaraz Salam, Jasper M Morrow, Robin Howard, et al.Orphanet Journal of Rare Diseases|September 28, 2024
Predictors of cardiac disease in duchenne muscular dystrophy: a systematic review and evidence gradingErik Landfeldt, Alberto Alemán, Sophia Abner, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 2, 2012
Comprehensive analysis of the TRPV4 gene in a large series of inherited neuropathies and controlsKatherine A Fawcett, Sinead M Murphy, James M Polke, et al.European Journal of Human Genetics : EJHG|August 14, 2014
Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literatureMerel Klaassens, Deborah Morrogh, Elisabeth M Rosser, et al.Pageof 1