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A L Andreu

Showing results (61-70 of 93) with videos related to

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Neurology|August 15, 2002
Phenotypic variability in a Spanish family with MNGIEJ Gamez, C Ferreiro, M L Accarino, et al.
British Journal of Sports Medicine|September 27, 2006
Can patients with McArdle's disease run?M Pérez, M Moran, C Cardona, et al.
Annals of Neurology|June 9, 1999
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 geneA L Andreu, K Tanji, C Bruno, et al.
Neurology|October 27, 2004
Lack of gastrointestinal symptoms in a 60-year-old patient with MNGIEM A Martín, A Blázquez, R Martí, et al.
Journal of the Neurological Sciences|July 13, 1999
A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathyG M Hadjigeorgiou, S H Kim, K H Fischbeck, et al.
Revista De Neurologia|September 19, 2007
[Private mutations in the myophosphorylase gene: the first case in a patient of Latin American descent]I Fernandez-Cadenas, G Nogales-Gadea, D Llige, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle diseaseInes Garcia-Consuegra, J C Rubio, G Nogales-Gadea, et al.
Genes, Brain, and Behavior|October 15, 2013
Identification and biochemical characterization of the novel mutation m.8839G>C in the mitochondrial ATP6 gene associated with NARP syndromeA Blanco-Grau, I Bonaventura-Ibars, J Coll-Cantí, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle diseaseInes Garcia-Consuegra, J C Rubio, G Nogales-Gadea, et al.
Journal of Medical Genetics|March 3, 2009
Novel mutations in patients with McArdle disease by analysis of skeletal muscle mRNAI García-Consuegra, J C Rubio, G Nogales-Gadea, et al.
Pageof 10

Showing results (61-70 of 93) with videos related to

Sort By:
Pageof 10
Neurology|August 15, 2002
Phenotypic variability in a Spanish family with MNGIEJ Gamez, C Ferreiro, M L Accarino, et al.
British Journal of Sports Medicine|September 27, 2006
Can patients with McArdle's disease run?M Pérez, M Moran, C Cardona, et al.
Annals of Neurology|June 9, 1999
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 geneA L Andreu, K Tanji, C Bruno, et al.
Neurology|October 27, 2004
Lack of gastrointestinal symptoms in a 60-year-old patient with MNGIEM A Martín, A Blázquez, R Martí, et al.
Journal of the Neurological Sciences|July 13, 1999
A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathyG M Hadjigeorgiou, S H Kim, K H Fischbeck, et al.
Revista De Neurologia|September 19, 2007
[Private mutations in the myophosphorylase gene: the first case in a patient of Latin American descent]I Fernandez-Cadenas, G Nogales-Gadea, D Llige, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle diseaseInes Garcia-Consuegra, J C Rubio, G Nogales-Gadea, et al.
Genes, Brain, and Behavior|October 15, 2013
Identification and biochemical characterization of the novel mutation m.8839G>C in the mitochondrial ATP6 gene associated with NARP syndromeA Blanco-Grau, I Bonaventura-Ibars, J Coll-Cantí, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle diseaseInes Garcia-Consuegra, J C Rubio, G Nogales-Gadea, et al.
Journal of Medical Genetics|March 3, 2009
Novel mutations in patients with McArdle disease by analysis of skeletal muscle mRNAI García-Consuegra, J C Rubio, G Nogales-Gadea, et al.
Pageof 10