Showing results (151-160 of 437) with videos related to
Sort By:
Pageof 44
Muscle & Nerve|January 1, 1978
Adult-onset acid maltase deficiency: a postmortem studyS DiMauro, L Z Stern, M Mehler, et al.The New England Journal of Medicine|March 11, 1976
Adult-onset acid maltase deficiency. Morphologic and biochemical abnormalities reproduced in in cultured muscleV Askanas, W K Engel, S DiMauro, et al.Molecular Genetics and Metabolism|May 18, 1999
Polymorphic variants in the human mitochondrial cytochrome b geneA L Andreu, C Bruno, G M Hadjigeorgiou, et al.Annals of Neurology|March 11, 1999
Kearns-Sayre syndrome: unusual pattern of expression of subunits of the respiratory chain in the cerebellar systemK Tanji, T H Vu, E A Schon, et al.Annals of Neurology|December 1, 1993
The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndromeF M Santorelli, S Shanske, A Macaya, et al.Neurology|June 1, 1982
Muscle phosphoglycerate mutase deficiencyS DiMauro, A F Miranda, M Olarte, et al.Journal of the Neurological Sciences|February 1, 1987
Peripheral neuropathy in mitochondrial diseaseG Pezeshkpour, C Krarup, F Buchthal, et al.Journal of the Neurological Sciences|April 1, 1979
Muscle carnitine deficiency. Genetic heterogeneityJ Willner, S DiMauro, A Eastwood, et al.Annals of Neurology|September 1, 1995
A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal necrosisD Thyagarajan, S Shanske, M Vazquez-Memije, et al.Muscle & Nerve|September 1, 1996
Molecular basis of muscle phosphoglycerate mutase (PGAM-M) deficiency in the Italian kindredA Toscano, S Tsujino, G Vita, et al.Pageof 44