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A L Andreu

Showing results (81-90 of 93) with videos related to

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International Journal of Sports Medicine|August 10, 2007
AMPD1 genotypes and exercise capacity in McArdle patientsJ C Rubio, M Pérez, J L Maté-Muñoz, et al.
Neurology|June 17, 1999
Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) geneC M Sue, K Tanji, G Hadjigeorgiou, et al.
Journal of Viral Hepatitis|March 27, 2007
Peginterferon alpha-2b plus ribavirin vs interferon alpha-2b plus ribavirin for chronic hepatitis C in HIV-coinfected patientsM Crespo, S Sauleda, J I Esteban, et al.
Journal of Medical Genetics|January 7, 2009
NARP syndrome in a patient harbouring an insertion in the MT-ATP6 gene that results in a truncated proteinE López-Gallardo, A Solano, M D Herrero-Martín, et al.
Neurology|August 13, 2003
A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2L Palenzuela, A L Andreu, J Gàmez, et al.
British Journal of Sports Medicine|July 10, 2007
The I allele of the ACE gene is associated with improved exercise capacity in women with McArdle diseaseF Gómez-Gallego, C Santiago, M Morán, et al.
Annals of Human Genetics|January 30, 2004
Molecular analysis of myophosphorylase deficiency in Dutch patients with McArdle's diseaseM A Martín, J C Rubio, R A Wevers, et al.
Molecular Metabolism|December 1, 2022
Low aerobic capacity in McArdle disease: A role for mitochondrial network impairment?M Villarreal-Salazar, A Santalla, A Real-Martínez, et al.
Annals of Neurology|November 15, 2001
Molecular heterogeneity of myophosphorylase deficiency (McArdle's disease): a genotype-phenotype correlation studyM A Martín, J C Rubio, J Buchbinder, et al.
Antimicrobial Agents and Chemotherapy|July 5, 2017
Influence of Mitochondrial Genetics on the Mitochondrial Toxicity of Linezolid in Blood Cells and Skin Nerve FibersG Garrabou, À Soriano, T Pinós, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
International Journal of Sports Medicine|August 10, 2007
AMPD1 genotypes and exercise capacity in McArdle patientsJ C Rubio, M Pérez, J L Maté-Muñoz, et al.
Neurology|June 17, 1999
Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) geneC M Sue, K Tanji, G Hadjigeorgiou, et al.
Journal of Viral Hepatitis|March 27, 2007
Peginterferon alpha-2b plus ribavirin vs interferon alpha-2b plus ribavirin for chronic hepatitis C in HIV-coinfected patientsM Crespo, S Sauleda, J I Esteban, et al.
Journal of Medical Genetics|January 7, 2009
NARP syndrome in a patient harbouring an insertion in the MT-ATP6 gene that results in a truncated proteinE López-Gallardo, A Solano, M D Herrero-Martín, et al.
Neurology|August 13, 2003
A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2L Palenzuela, A L Andreu, J Gàmez, et al.
British Journal of Sports Medicine|July 10, 2007
The I allele of the ACE gene is associated with improved exercise capacity in women with McArdle diseaseF Gómez-Gallego, C Santiago, M Morán, et al.
Annals of Human Genetics|January 30, 2004
Molecular analysis of myophosphorylase deficiency in Dutch patients with McArdle's diseaseM A Martín, J C Rubio, R A Wevers, et al.
Molecular Metabolism|December 1, 2022
Low aerobic capacity in McArdle disease: A role for mitochondrial network impairment?M Villarreal-Salazar, A Santalla, A Real-Martínez, et al.
Annals of Neurology|November 15, 2001
Molecular heterogeneity of myophosphorylase deficiency (McArdle's disease): a genotype-phenotype correlation studyM A Martín, J C Rubio, J Buchbinder, et al.
Antimicrobial Agents and Chemotherapy|July 5, 2017
Influence of Mitochondrial Genetics on the Mitochondrial Toxicity of Linezolid in Blood Cells and Skin Nerve FibersG Garrabou, À Soriano, T Pinós, et al.
Pageof 10