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Neurology|September 11, 2002
Premorbid weight, body mass, and varsity athletics in ALSN Scarmeas, T Shih, Y Stern, et al.Neurology|October 1, 1994
Familial aggregation of amyotrophic lateral sclerosis, dementia, and Parkinson's disease: evidence of shared genetic susceptibilityD Majoor-Krakauer, R Ottman, W G Johnson, et al.Biochemical and Biophysical Research Communications|April 28, 1989
Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndromeC T Moraes, E A Schon, S DiMauro, et al.The Journal of Clinical Investigation|November 1, 1987
Characterization of the enzymatic defect in late-onset muscle phosphofructokinase deficiency. New subtype of glycogen storage disease type VIIS Vora, S DiMauro, D Spear, et al.Journal of Applied Physiology (Bethesda, Md. : 1985)|February 1, 1989
Metabolic and functional adaptation of the diaphragm to training with resistive loadsS R Akabas, A R Bazzy, S DiMauro, et al.Neurology|November 1, 1979
Phosphorylase isoenzymes in normal and myophosphorylase-deficient human heartA F Miranda, E G Nette, P L Hartlage, et al.Neurology|October 1, 1983
Congenital myopathy due to phosphorylase deficiencyF Cornelio, N Bresolin, S DiMauro, et al.American Journal of Diseases of Children (1960)|July 1, 1982
Encephalopathy and fatal myopathy in two siblings. Their association with partial deficiency of muscle carnitineD Parker, A W Root, S Schimmel, et al.Biochimica Et Biophysica Acta|August 26, 1998
Mitochondria in neuromuscular disordersS DiMauro, E Bonilla, M Davidson, et al.Neuromuscular Disorders : NMD|January 1, 1992
Polysaccharide storage myopathy associated with recurrent exertional rhabdomyolysis in horsesS J Valberg, G H Cardinet, G P Carlson, et al.Pageof 44