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S Shanske

Showing results (41-50 of 141) with videos related to

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Neurology|June 1, 1986
Juvenile-onset acid maltase deficiency with unusual familial featuresM J Danon, S DiMauro, S Shanske, et al.
Neurology|April 24, 2002
Exercise-induced muscle "burning," fatigue, and hyper-CKemia: mtDNA T10010C mutation in tRNA(Gly)Y Nishigaki, E Bonilla, S Shanske, et al.
Mutation Research|October 23, 1997
Oxidative phosphorylation dysfunction does not increase the rate of accumulation of age-related mtDNA deletions in skeletal muscleC H Tengan, A A Gabbai, S Shanske, et al.
Human Mutation|January 1, 1996
Identification of a mutation in the mitochondrial tRNA(Cys) gene associated with mitochondrial encephalopathyG Manfredi, E A Schon, E Bonilla, et al.
Neurology|March 1, 1994
Clinical and biochemical features of 10 adult patients with muscle phosphorylase kinase deficiencyD A Wilkinson, P Tonin, S Shanske, et al.
Neurology|January 27, 1998
Combined defects of muscle phosphofructokinase and AMP deaminase in a child with myoglobinuriaC Bruno, C Minetti, S Shanske, et al.
Molecular and Cellular Biology|March 1, 1991
Replication-competent human mitochondrial DNA lacking the heavy-strand promoter regionC T Moraes, F Andreetta, E Bonilla, et al.
Lancet (London, England)|March 2, 1991
Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathyE Arnaudo, M Dalakas, S Shanske, et al.
Neuromuscular Disorders : NMD|January 1, 1996
Cloning of bovine muscle glycogen phosphorylase cDNA and identification of a mutation in cattle with myophosphorylase deficiency, an animal model for McArdle's diseaseS Tsujino, S Shanske, S J Valberg, et al.
Neurology|May 1, 1994
A T-->C mutation at nt 8993 of mitochondrial DNA in a child with Leigh syndromeF M Santorelli, S Shanske, K D Jain, et al.
Pageof 15

Showing results (41-50 of 141) with videos related to

Sort By:
Pageof 15
Neurology|June 1, 1986
Juvenile-onset acid maltase deficiency with unusual familial featuresM J Danon, S DiMauro, S Shanske, et al.
Neurology|April 24, 2002
Exercise-induced muscle "burning," fatigue, and hyper-CKemia: mtDNA T10010C mutation in tRNA(Gly)Y Nishigaki, E Bonilla, S Shanske, et al.
Mutation Research|October 23, 1997
Oxidative phosphorylation dysfunction does not increase the rate of accumulation of age-related mtDNA deletions in skeletal muscleC H Tengan, A A Gabbai, S Shanske, et al.
Human Mutation|January 1, 1996
Identification of a mutation in the mitochondrial tRNA(Cys) gene associated with mitochondrial encephalopathyG Manfredi, E A Schon, E Bonilla, et al.
Neurology|March 1, 1994
Clinical and biochemical features of 10 adult patients with muscle phosphorylase kinase deficiencyD A Wilkinson, P Tonin, S Shanske, et al.
Neurology|January 27, 1998
Combined defects of muscle phosphofructokinase and AMP deaminase in a child with myoglobinuriaC Bruno, C Minetti, S Shanske, et al.
Molecular and Cellular Biology|March 1, 1991
Replication-competent human mitochondrial DNA lacking the heavy-strand promoter regionC T Moraes, F Andreetta, E Bonilla, et al.
Lancet (London, England)|March 2, 1991
Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathyE Arnaudo, M Dalakas, S Shanske, et al.
Neuromuscular Disorders : NMD|January 1, 1996
Cloning of bovine muscle glycogen phosphorylase cDNA and identification of a mutation in cattle with myophosphorylase deficiency, an animal model for McArdle's diseaseS Tsujino, S Shanske, S J Valberg, et al.
Neurology|May 1, 1994
A T-->C mutation at nt 8993 of mitochondrial DNA in a child with Leigh syndromeF M Santorelli, S Shanske, K D Jain, et al.
Pageof 15