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L Andreu

Showing results (231-240 of 313) with videos related to

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Neuroscience Letters|July 17, 2007
Genotype modulators of clinical severity in McArdle diseaseJuan C Rubio, Félix Gómez-Gallego, Catalina Santiago, et al.
American Journal of Human Genetics|August 12, 1999
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IVC Bruno, A Martinuzzi, Y Tang, et al.
Neuromuscular Disorders : NMD|June 19, 2001
A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathyY Campos, J Gámez, A García, et al.
Neuromuscular Disorders : NMD|February 5, 2013
Identification of the novel mutation m.5658T>C in the mitochondrial tRNA(Asn) gene in a patient with myopathy, bilateral ptosis and ophthalmoparesisTomàs Pinós, Maria Jesús Melià, Nicolau Ortiz, et al.
Annals of Neurology|January 23, 1999
A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuriaA L Andreu, C Bruno, T C Dunne, et al.
Plos One|July 23, 2021
Clinical characteristics of COVID-19 in older adults. A retrospective study in long-term nursing homes in CataloniaUxío Meis-Pinheiro, Francesc Lopez-Segui, Sandra Walsh, et al.
Human Mutation|November 13, 2007
Expression of the muscle glycogen phosphorylase gene in patients with McArdle disease: the role of nonsense-mediated mRNA decayGisela Nogales-Gadea, Juan Carlos Rubio, Israel Fernandez-Cadenas, et al.
Neurology|February 27, 2001
Autosomal dominant limb-girdle muscular dystrophy: a large kindred with evidence for anticipationJ Gamez, C Navarro, A L Andreu, et al.
Biomedicine Hub|February 10, 2021
Digitalisation and COVID-19: The Perfect StormDenis Horgan, Joanne Hackett, C Benedikt Westphalen, et al.
Genes|January 21, 2022
Preclinical Research in McArdle Disease: A Review of Research Models and Therapeutic StrategiesMónica Villarreal-Salazar, Astrid Brull, Gisela Nogales-Gadea, et al.
Pageof 32

Showing results (231-240 of 313) with videos related to

Sort By:
Pageof 32
Neuroscience Letters|July 17, 2007
Genotype modulators of clinical severity in McArdle diseaseJuan C Rubio, Félix Gómez-Gallego, Catalina Santiago, et al.
American Journal of Human Genetics|August 12, 1999
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IVC Bruno, A Martinuzzi, Y Tang, et al.
Neuromuscular Disorders : NMD|June 19, 2001
A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathyY Campos, J Gámez, A García, et al.
Neuromuscular Disorders : NMD|February 5, 2013
Identification of the novel mutation m.5658T>C in the mitochondrial tRNA(Asn) gene in a patient with myopathy, bilateral ptosis and ophthalmoparesisTomàs Pinós, Maria Jesús Melià, Nicolau Ortiz, et al.
Annals of Neurology|January 23, 1999
A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuriaA L Andreu, C Bruno, T C Dunne, et al.
Plos One|July 23, 2021
Clinical characteristics of COVID-19 in older adults. A retrospective study in long-term nursing homes in CataloniaUxío Meis-Pinheiro, Francesc Lopez-Segui, Sandra Walsh, et al.
Human Mutation|November 13, 2007
Expression of the muscle glycogen phosphorylase gene in patients with McArdle disease: the role of nonsense-mediated mRNA decayGisela Nogales-Gadea, Juan Carlos Rubio, Israel Fernandez-Cadenas, et al.
Neurology|February 27, 2001
Autosomal dominant limb-girdle muscular dystrophy: a large kindred with evidence for anticipationJ Gamez, C Navarro, A L Andreu, et al.
Biomedicine Hub|February 10, 2021
Digitalisation and COVID-19: The Perfect StormDenis Horgan, Joanne Hackett, C Benedikt Westphalen, et al.
Genes|January 21, 2022
Preclinical Research in McArdle Disease: A Review of Research Models and Therapeutic StrategiesMónica Villarreal-Salazar, Astrid Brull, Gisela Nogales-Gadea, et al.
Pageof 32