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Molecular and Cellular Biochemistry|October 6, 1997
Carnitine palmitoyltransferase II deficiency: diagnosis by molecular analysis of bloodP Kaufmann, M el-Schahawi, S DiMauroArchives of Pediatrics & Adolescent Medicine|November 29, 2001
The other human genomeA L Shanske, S Shanske, S DiMauroJournal of Bioenergetics and Biomembranes|April 1, 1997
Mitochondrial DNA mutations and pathogenesisE A Schon, E Bonilla, S DiMauroAnnals of Neurology|January 1, 1983
Phosphoglycerate kinase deficiency: another cause of recurrent myoglobinuriaS DiMauro, M Dalakas, A F MirandaAdvances in Pediatrics|January 1, 1990
Recurrent childhood myoglobinuriaI Tein, S DiMauro, D C DeVivoRevista De Neurologia|April 2, 1999
[Mitochondrial encephalopathies: where are we going?]S DiMauro, A L Andreu, E BonillaNeurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 31, 2001
Mitochondrial encephalomyopathies: therapeutic approachesS DiMauro, M Hirano, E A SchonNeurology|July 1, 1978
Active transport of carnitine into skeletal muscleJ H Willner, S Ginsburg, S DimauroCRC Critical Reviews in Clinical Neurobiology|January 1, 1984
Disorders of glycogen metabolism of muscleS DiMauro, N Bresolin, A P HaysJournal of Bioenergetics and Biomembranes|June 1, 1994
Mitochondrial encephalomyopathies: clinical and molecular analysisE A Schon, M Hirano, S DiMauroPageof 44