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Presse Medicale (Paris, France : 1983)|October 20, 1999
[Muscle contractures. Essay on a physiopathological approach to clarify the nomenclature]G Serratrice, L P RowlandScience (New York, N.Y.)|November 20, 1973
Muscle carnitine palmityltransferase deficiency and myoglobinuriaS DiMauro, P M DiMauroNeurology|November 1, 1978
Fatal infantile form of muscle phosphorylase deficiencyS DiMauro, P L HartlageBrain Pathology (Zurich, Switzerland)|July 8, 2000
Mutations in mtDNA: are we scraping the bottom of the barrel?S DiMauro, A L AndreuAnnals of Medicine|October 30, 2001
Mutations in mitochondrial DNA as a cause of exercise intoleranceS DiMauro, A L AndreuArquivos De Neuro-Psiquiatria|December 1, 1989
[Myopathy due to succinate cytochrome C oxidoreductase deficiency: possible defect of complex II of the respiratory chain]L C Werneck, S DiMauroAmerican Journal of Medical Genetics|October 2, 2001
Mitochondrial DNA mutations in human diseaseS DiMauro, E A SchonBiology of the Neonate|January 1, 1990
Mitochondrial defects of brain and muscleD C De Vivo, S DiMauroThe Journal of Pediatrics|September 1, 1994
Myophosphorylase deficiency: an unusually severe form with myoglobinuriaK Kristjánsson, S Tsujino, S DiMauroPageof 44