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The Journal of Pediatrics|November 1, 1982
Carnitine deficiency presenting as familial cardiomyopathy: a treatable defect in carnitine transportL J Waber, D Valle, C Neill, et al.Seminars in Perinatology|May 20, 1999
Neonatal presentations of mitochondrial metabolic disordersC M Sue, M Hirano, S DiMauro, et al.Neurology|October 22, 1998
Mitochondrial DNA depletion in a patient with long survivalT H Vu, K Tanji, H Valsamis, et al.Pediatric Neurology|September 1, 1996
Novel mutation in the mitochondrial DNA tRNA glycine gene associated with sudden unexpected deathF M Santorelli, J S Schlessel, A E Slonim, et al.Gene|September 30, 1988
Subunit Va of human and bovine cytochrome c oxidase is highly conservedR Rizzuto, H Nakase, M Zeviani, et al.Pediatric Research|September 1, 1993
Valproic acid impairs carnitine uptake in cultured human skin fibroblasts. An in vitro model for the pathogenesis of valproic acid-associated carnitine deficiencyI Tein, S DiMauro, Z W Xie, et al.Neurology|September 1, 1996
Complications of intravenous immune globulin treatment in neurologic diseaseT H Brannagan, K J Nagle, D J Lange, et al.Pediatric Research|August 29, 2000
A missense mutation in the mitochondrial cytochrome b gene in a revisited case with histiocytoid cardiomyopathyA L Andreu, N Checcarelli, S Iwata, et al.Pediatric Research|October 1, 1984
Histiocytoid cardiomyopathy of infancy: deficiency of reducible cytochrome b in heart mitochondriaA Papadimitriou, H B Neustein, S Dimauro, et al.Pageof 44