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Antoni L Andreu

Showing results (21-30 of 77) with videos related to

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Journal of Cellular Physiology|February 9, 2017
Role of PARP activity in lung cancer-induced cachexia: Effects on muscle oxidative stress, proteolysis, anabolic markers, and phenotypeAlba Chacon-Cabrera, Mercè Mateu-Jimenez, Klaus Langohr, et al.
Journal of Child Neurology|August 24, 2007
Exercise capacity in a child with McArdle diseaseMargarita Pérez, José L Maté-Muñoz, Carl Foster, et al.
Biochemical and Biophysical Research Communications|October 13, 2012
Functional outcome of a novel SLC29A3 mutation identified in a patient with H syndromeIsabel Huber-Ruano, Ekaitz Errasti-Murugarren, Valeria Godoy, et al.
Human Mutation|April 28, 2015
McArdle Disease: Update of Reported Mutations and Polymorphisms in the PYGM GeneGisela Nogales-Gadea, Astrid Brull, Alfredo Santalla, et al.
Mitochondrion|September 4, 2010
A novel mutation in the mitochondrial tRNA(Ala) gene (m.5636T>C) in a patient with progressive external ophthalmoplegiaTomàs Pinós, Mario Marotta, Eduard Gallardo, et al.
Archives of Neurology|December 19, 2006
Novel mutation in the PYGM gene resulting in McArdle diseaseJuan C Rubio, Alejandro Lucia, Israel Fernández-Cadenas, et al.
Disease Models & Mechanisms|March 13, 2015
Sodium valproate increases the brain isoform of glycogen phosphorylase: looking for a compensation mechanism in McArdle disease using a mouse primary skeletal-muscle culture in vitroNoemí de Luna, Astrid Brull, Josep Maria Guiu, et al.
The Journal of Physiology|April 16, 2015
Phenotype consequences of myophosphorylase dysfunction: insights from the McArdle mouse modelAstrid Brull, Noemí de Luna, Albert Blanco-Grau, et al.
Archives of Neurology|April 13, 2005
Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 geneMiguel A Martín, Alberto Blázquez, Luis G Gutierrez-Solana, et al.
Human Mutation|January 16, 2007
A proposed molecular diagnostic flowchart for myophosphorylase deficiency (McArdle disease) in blood samples from Spanish patientsJuan C Rubio, Ines Garcia-Consuegra, Gisela Nogales-Gadea, et al.
Pageof 8

Showing results (21-30 of 77) with videos related to

Sort By:
Pageof 8
Journal of Cellular Physiology|February 9, 2017
Role of PARP activity in lung cancer-induced cachexia: Effects on muscle oxidative stress, proteolysis, anabolic markers, and phenotypeAlba Chacon-Cabrera, Mercè Mateu-Jimenez, Klaus Langohr, et al.
Journal of Child Neurology|August 24, 2007
Exercise capacity in a child with McArdle diseaseMargarita Pérez, José L Maté-Muñoz, Carl Foster, et al.
Biochemical and Biophysical Research Communications|October 13, 2012
Functional outcome of a novel SLC29A3 mutation identified in a patient with H syndromeIsabel Huber-Ruano, Ekaitz Errasti-Murugarren, Valeria Godoy, et al.
Human Mutation|April 28, 2015
McArdle Disease: Update of Reported Mutations and Polymorphisms in the PYGM GeneGisela Nogales-Gadea, Astrid Brull, Alfredo Santalla, et al.
Mitochondrion|September 4, 2010
A novel mutation in the mitochondrial tRNA(Ala) gene (m.5636T>C) in a patient with progressive external ophthalmoplegiaTomàs Pinós, Mario Marotta, Eduard Gallardo, et al.
Archives of Neurology|December 19, 2006
Novel mutation in the PYGM gene resulting in McArdle diseaseJuan C Rubio, Alejandro Lucia, Israel Fernández-Cadenas, et al.
Disease Models & Mechanisms|March 13, 2015
Sodium valproate increases the brain isoform of glycogen phosphorylase: looking for a compensation mechanism in McArdle disease using a mouse primary skeletal-muscle culture in vitroNoemí de Luna, Astrid Brull, Josep Maria Guiu, et al.
The Journal of Physiology|April 16, 2015
Phenotype consequences of myophosphorylase dysfunction: insights from the McArdle mouse modelAstrid Brull, Noemí de Luna, Albert Blanco-Grau, et al.
Archives of Neurology|April 13, 2005
Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 geneMiguel A Martín, Alberto Blázquez, Luis G Gutierrez-Solana, et al.
Human Mutation|January 16, 2007
A proposed molecular diagnostic flowchart for myophosphorylase deficiency (McArdle disease) in blood samples from Spanish patientsJuan C Rubio, Ines Garcia-Consuegra, Gisela Nogales-Gadea, et al.
Pageof 8