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American Journal of Human Genetics|May 1, 1992
The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscleC T Moraes, E Ricci, E Bonilla, et al.Neurologia I Neurochirurgia Polska|January 11, 2002
[Pathomechanism and clinical presentation of neurobehavioral disturbances in a patient with MELAS syndrome]M Pachalska, S DiMauro, B D MacQueen, et al.The Journal of Clinical Investigation|August 1, 1983
Muscle phosphofructokinase deficiency. Biochemical and immunological studies of phosphofructokinase isozymes in muscle cultureM Davidson, A F Miranda, A N Bender, et al.Nature|May 25, 1989
An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop regionM Zeviani, S Servidei, C Gellera, et al.Annals of Neurology|December 1, 1988
McArdle's disease: biochemical and molecular genetic studiesS Servidei, S Shanske, M Zeviani, et al.The Journal of Biological Chemistry|October 25, 1987
Isolation of a cDNA encoding the muscle-specific subunit of human phosphoglycerate mutaseS Shanske, S Sakoda, M A Hermodson, et al.Neurology|August 3, 1999
A prospective study of preferences and actual treatment choices in ALSS M Albert, P L Murphy, M L Del Bene, et al.Neurology|June 3, 2009
Clinical features that distinguish PLS, upper motor neuron-dominant ALS, and typical ALSP H Gordon, B Cheng, I B Katz, et al.Neurology|August 1, 1983
Muscle phosphoglycerate mutase (PGAM) deficiency: a second caseN Bresolin, Y I Ro, M Reyes, et al.Human Molecular Genetics|January 1, 1994
Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathyM Sciacco, E Bonilla, E A Schon, et al.Pageof 44