Showing results (111-120 of 437) with videos related to
Sort By:
Pageof 44
Archives of Neurology|April 1, 1985
Immunocytochemical analysis of normal and acid maltase-deficient muscle culturesA F Miranda, S Shanske, A P Hays, et al.Pediatric Research|October 1, 1981
Mucolipidosis II (I-cell disease): studies of muscle biopsy and muscle culturesS Shanske, A F Miranda, A S Penn, et al.Muscle & Nerve. Supplement|January 1, 1995
Molecular genetic studies in muscle phosphoglycerate mutase (PGAM-M) deficiencyS Tsujino, S Shanske, S Sakoda, et al.Journal of Inherited Metabolic Disease|January 1, 1993
Skin fibroblast carnitine uptake in secondary carnitine deficiency disordersI Tein, D C De Vivo, D Ranucci, et al.Neurology|February 1, 1975
Hereditary carnitine deficiency of muscleD H VanDyke, R C Griggs, W Markesbery, et al.Neurology|May 1, 1994
Clinical and morphologic features of a myopathy associated with a point mutation in the mitochondrial tRNA(Pro) geneV V Ionasescu, M Hart, S DiMauro, et al.Neurology|January 1, 1987
Benign reversible muscle cytochrome c oxidase deficiency: a second caseM Zeviani, P Peterson, S Servidei, et al.Muscle & Nerve|August 1, 1994
Ekbom's syndrome: lipomas, ataxia, and neuropathy with MERRFP A Calabresi, G Silvestri, S DiMauro, et al.Muscle & Nerve|October 1, 1985
Beta-oxidation enzymes in normal human muscle and in muscle from a patient with an unusual form of myopathic carnitine deficiencyC P Trevisan, H Reichmann, D C DeVivo, et al.Annals of Neurology|April 1, 1979
Transfer factor is ineffective in amyotrophic lateral sclerosisM R Olarte, J C Gersten, J Zabriskie, et al.Pageof 44