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Birth Defects Original Article Series|January 1, 1975
Three familial midline malformtion syndromes of the central nervous system: agenesis of the corpus callosum and anterior horn-cell disease; agenesis of cerebellar vermis; and atrophy of the cerebellar vermisE Andermann, F Andermann, M Joubert, et al.The American Journal of Pathology|June 1, 1991
Inhibition of myosatellite cell proliferation by gamma irradiation does not prevent the age-related increase of the number of dystrophin-positive fibers in soleus muscles of mdx female heterozygote miceB Weller, G Karpati, S Lehnert, et al.Revue Neurologique|January 1, 1991
Correlative multidisciplinary approach to the study of mitochondrial encephalomyopathiesG Karpati, D Arnold, P Matthews, et al.Muscle & Nerve|June 1, 1987
Glucocorticoid excess induces preferential depletion of myosin in denervated skeletal muscle fibersG Rouleau, G Karpati, S Carpenter, et al.Brain : a Journal of Neurology|October 1, 1988
Familial myopathy with changes resembling inclusion body myositis and periventricular leucoencephalopathy. A new syndromeA J Cole, R Kuzniecky, G Karpati, et al.Archives of Neurology|December 1, 1985
Hexosaminidase-A deficiency presenting as atypical juvenile-onset spinal muscular atrophyS Parnes, G Karpati, S Carpenter, et al.Journal of Neuropathology and Experimental Neurology|March 1, 1993
Localization and quantitation of the chromosome 6-encoded dystrophin-related protein in normal and pathological human muscleG Karpati, S Carpenter, G E Morris, et al.Journal of the Neurological Sciences|October 1, 1988
Adult onset motor neuronopathy in the juvenile type of hexosaminidase A and B deficiencyM Rubin, G Karpati, L S Wolfe, et al.Neurology|January 1, 1991
In vivo muscle magnetic resonance spectroscopy in the clinical investigation of mitochondrial diseaseP M Matthews, C Allaire, E A Shoubridge, et al.Current Opinion in Neurology and Neurosurgery|October 1, 1992
Recent developments in the biology of dystrophin and related moleculesG KarpatiPageof 90