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A Genge

Showing results (1-10 of 14) with videos related to

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Neuroepidemiology|June 5, 2009
Incidence and prevalence of amyotrophic lateral sclerosis in Canada: a systematic review of the literatureC Wolfson, S Kilborn, M Oskoui, et al.
Journal of Clinical Neuromuscular Disease|December 17, 2008
Muscle diseasesA Genge, A H Shapira, R C Griggs
Neuroreport|July 17, 1998
Recovery of N-acetylaspartate in corticomotor neurons of patients with ALS after riluzole therapyS Kalra, N R Cashman, A Genge, et al.
Neuromuscular Disorders : NMD|March 1, 1995
Familial myopathy with conspicuous depletion of mitochondria in muscle fibers: a morphologically distinct diseaseA Genge, G Karpati, D Arnold, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 13, 2006
Cerebral degeneration predicts survival in amyotrophic lateral sclerosisS Kalra, A Vitale, N R Cashman, et al.
Human Molecular Genetics|November 1, 1996
A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapyK Fu, R Hartlen, T Johns, et al.
Journal of Neuropathology and Experimental Neurology|May 22, 1998
Characterization of the mitochondrial DNA abnormalities in the skeletal muscle of patients with inclusion body myositisR Horvath, K Fu, T Johns, et al.
Journal of Neuromuscular Diseases|November 19, 2016
Screening for Pompe Disease in Specific At-Risk Populations with Sleep-Disordered BreathingM Kaminska, F Noel, A Genge, et al.
Muscle & Nerve|October 15, 1998
Intracellular phosphates in inclusion body myositis--a 31P magnetic resonance spectroscopy studyZ Argov, T Taivassalo, N De Stefano, et al.
Neurology|June 1, 1995
Short-term dichloroacetate treatment improves indices of cerebral metabolism in patients with mitochondrial disordersN De Stefano, P M Matthews, B Ford, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Neuroepidemiology|June 5, 2009
Incidence and prevalence of amyotrophic lateral sclerosis in Canada: a systematic review of the literatureC Wolfson, S Kilborn, M Oskoui, et al.
Journal of Clinical Neuromuscular Disease|December 17, 2008
Muscle diseasesA Genge, A H Shapira, R C Griggs
Neuroreport|July 17, 1998
Recovery of N-acetylaspartate in corticomotor neurons of patients with ALS after riluzole therapyS Kalra, N R Cashman, A Genge, et al.
Neuromuscular Disorders : NMD|March 1, 1995
Familial myopathy with conspicuous depletion of mitochondria in muscle fibers: a morphologically distinct diseaseA Genge, G Karpati, D Arnold, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 13, 2006
Cerebral degeneration predicts survival in amyotrophic lateral sclerosisS Kalra, A Vitale, N R Cashman, et al.
Human Molecular Genetics|November 1, 1996
A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapyK Fu, R Hartlen, T Johns, et al.
Journal of Neuropathology and Experimental Neurology|May 22, 1998
Characterization of the mitochondrial DNA abnormalities in the skeletal muscle of patients with inclusion body myositisR Horvath, K Fu, T Johns, et al.
Journal of Neuromuscular Diseases|November 19, 2016
Screening for Pompe Disease in Specific At-Risk Populations with Sleep-Disordered BreathingM Kaminska, F Noel, A Genge, et al.
Muscle & Nerve|October 15, 1998
Intracellular phosphates in inclusion body myositis--a 31P magnetic resonance spectroscopy studyZ Argov, T Taivassalo, N De Stefano, et al.
Neurology|June 1, 1995
Short-term dichloroacetate treatment improves indices of cerebral metabolism in patients with mitochondrial disordersN De Stefano, P M Matthews, B Ford, et al.
Pageof 2