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Neuroepidemiology
|
June 5, 2009
Incidence and prevalence of amyotrophic lateral sclerosis in Canada: a systematic review of the literature
C Wolfson, S Kilborn, M Oskoui, et al.
Journal of Clinical Neuromuscular Disease
|
December 17, 2008
Muscle diseases
A Genge, A H Shapira, R C Griggs
Neuroreport
|
July 17, 1998
Recovery of N-acetylaspartate in corticomotor neurons of patients with ALS after riluzole therapy
S 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 disease
A Genge, G Karpati, D Arnold, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 13, 2006
Cerebral degeneration predicts survival in amyotrophic lateral sclerosis
S 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 therapy
K 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 myositis
R 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 Breathing
M Kaminska, F Noel, A Genge, et al.
Muscle & Nerve
|
October 15, 1998
Intracellular phosphates in inclusion body myositis--a 31P magnetic resonance spectroscopy study
Z 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 disorders
N De Stefano, P M Matthews, B Ford, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Neuroepidemiology
|
June 5, 2009
Incidence and prevalence of amyotrophic lateral sclerosis in Canada: a systematic review of the literature
C Wolfson, S Kilborn, M Oskoui, et al.
Journal of Clinical Neuromuscular Disease
|
December 17, 2008
Muscle diseases
A Genge, A H Shapira, R C Griggs
Neuroreport
|
July 17, 1998
Recovery of N-acetylaspartate in corticomotor neurons of patients with ALS after riluzole therapy
S 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 disease
A Genge, G Karpati, D Arnold, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 13, 2006
Cerebral degeneration predicts survival in amyotrophic lateral sclerosis
S 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 therapy
K 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 myositis
R 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 Breathing
M Kaminska, F Noel, A Genge, et al.
Muscle & Nerve
|
October 15, 1998
Intracellular phosphates in inclusion body myositis--a 31P magnetic resonance spectroscopy study
Z 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 disorders
N De Stefano, P M Matthews, B Ford, et al.
Page
of 2