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Journal of the Neurological Sciences|April 30, 1998
Cerebrospinal fluid carnitine levels in patients with Alzheimer's diseaseJ C Rubio, F de Bustos, J A Molina, et al.Neuromuscular Disorders : NMD|June 12, 2003
Two pathogenic mutations in the mitochondrial DNA tRNA Leu(UUR) gene (T3258C and A3280G) resulting in variable clinical phenotypesY Campos, A García, P del Hoyo, et al.Annals of Neurology|September 18, 2001
Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II geneY Campos, A García-Redondo, M A Fernández-Moreno, et al.International Journal of Sports Medicine|March 12, 2009
Genotype distributions in top-level soccer players: a role for ACE?P Juffer, R Furrer, M González-Freire, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|January 1, 1997
Cerebrospinal fluid levels of alpha-tocopherol (vitamin E) in Alzheimer's diseaseF J Jiménez-Jiménez, F de Bustos, J A Molina, 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.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.Revista De Neurologia|October 15, 2005
[Mitochondrial respiratory chain diseases. Evaluation and variability in 52 patients]F J Arpa-Gutiérrez, A Cruz-Martínez, Y Campos-González, et al.Pageof 5