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Showing results (161-170 of 421) with videos related to

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The Journal of Biological Chemistry|October 25, 1987
Isolation of a cDNA encoding the muscle-specific subunit of human phosphoglycerate mutaseS Shanske, S Sakoda, M A Hermodson, et al.
Neurology|August 1, 1983
Muscle phosphoglycerate mutase (PGAM) deficiency: a second caseN Bresolin, Y I Ro, M Reyes, et al.
Human Molecular Genetics|January 1, 1994
Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathyM Sciacco, E Bonilla, E A Schon, et al.
Neurology|November 30, 2000
Mitochondrial analysis in autosomal dominant hereditary spastic paraplegiaP Hedera, S DiMauro, E Bonilla, et al.
American Journal of Human Genetics|May 1, 1994
Identification of three novel mutations in non-Ashkenazi Italian patients with muscle phosphofructokinase deficiencyS Tsujino, S Servidei, P Tonin, et al.
Neuromuscular Disorders : NMD|July 1, 1995
Double trouble: combined myophosphorylase and AMP deaminase deficiency in a child homozygous for nonsense mutations at both lociS Tsujino, S Shanske, J E Carroll, et al.
Journal of the Neurological Sciences|September 1, 1991
Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: a new approach to the study of mitochondrial myopathiesF Andreetta, H J Tritschler, E A Schon, et al.
Chest|March 1, 1992
Respiratory failure revealing mitochondrial myopathy in adultsD Cros, S Palliyath, S DiMauro, et al.
Biofactors (Oxford, England)|December 20, 2008
Human CoQ10 deficienciesC M Quinzii, L C López, A Naini, et al.
Journal of Child Neurology|April 1, 1990
Cytochrome c oxidase deficiency in muscle with dicarboxylic aciduria and renal tubular acidosisG Pintos-Morell, R Haas, C Prodanos, et al.
Pageof 43

Showing results (161-170 of 421) with videos related to

Sort By:
Pageof 43
The Journal of Biological Chemistry|October 25, 1987
Isolation of a cDNA encoding the muscle-specific subunit of human phosphoglycerate mutaseS Shanske, S Sakoda, M A Hermodson, et al.
Neurology|August 1, 1983
Muscle phosphoglycerate mutase (PGAM) deficiency: a second caseN Bresolin, Y I Ro, M Reyes, et al.
Human Molecular Genetics|January 1, 1994
Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathyM Sciacco, E Bonilla, E A Schon, et al.
Neurology|November 30, 2000
Mitochondrial analysis in autosomal dominant hereditary spastic paraplegiaP Hedera, S DiMauro, E Bonilla, et al.
American Journal of Human Genetics|May 1, 1994
Identification of three novel mutations in non-Ashkenazi Italian patients with muscle phosphofructokinase deficiencyS Tsujino, S Servidei, P Tonin, et al.
Neuromuscular Disorders : NMD|July 1, 1995
Double trouble: combined myophosphorylase and AMP deaminase deficiency in a child homozygous for nonsense mutations at both lociS Tsujino, S Shanske, J E Carroll, et al.
Journal of the Neurological Sciences|September 1, 1991
Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: a new approach to the study of mitochondrial myopathiesF Andreetta, H J Tritschler, E A Schon, et al.
Chest|March 1, 1992
Respiratory failure revealing mitochondrial myopathy in adultsD Cros, S Palliyath, S DiMauro, et al.
Biofactors (Oxford, England)|December 20, 2008
Human CoQ10 deficienciesC M Quinzii, L C López, A Naini, et al.
Journal of Child Neurology|April 1, 1990
Cytochrome c oxidase deficiency in muscle with dicarboxylic aciduria and renal tubular acidosisG Pintos-Morell, R Haas, C Prodanos, et al.
Pageof 43