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Neurology|September 1, 1988
Deletions of mitochondrial DNA in Kearns-Sayre syndromeM Zeviani, C T Moraes, S DiMauro, et al.Muscle & Nerve|January 1, 1979
Lipid storage myopathy, ichthyosis, and steatorrheaA Miranda, S DiMauro, A Eastwood, et al.Annals of Neurology|August 1, 1997
Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?G Manfredi, T Vu, E Bonilla, et al.Neuromuscular Disorders : NMD|January 1, 1992
Melas: an original case and clinical criteria for diagnosisM Hirano, E Ricci, M R Koenigsberger, et al.Neurology|September 1, 1988
Kearns-Sayre syndrome in twins: lethal dominant mutation or acquired disease?L P Rowland, I Hausmanowa-Petrusewicz, B Bardurska, et al.Neurology|October 1, 1988
Immunocytochemical study of nebulin in Duchenne muscular dystrophyE Bonilla, A F Miranda, A Prelle, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 15, 2011
Pathogenesis and treatment of mitochondrial myopathies: recent advancesS DiMauroJournal of Inherited Metabolic Disease|January 1, 1996
Mitochondrial encephalomyopathies: what next?S DiMauroSeminars in Cell & Developmental Biology|December 12, 2001
Lessons from mitochondrial DNA mutationsS DiMauroItalian Journal of Neurological Sciences|August 11, 2000
Exercise intolerance and the mitochondrial respiratory chainS DiMauroPageof 44