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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.Journal of the Neurological Sciences|February 12, 1997
Cerebrospinal fluid carnitine levels in patients with Parkinson's diseaseF J Jiménez-Jiménez, J C Rubio, J A Molina, et al.International Journal of Sports Medicine|June 13, 2006
Does the C34T mutation in AMPD1 alter exercise capacity in the elderly?M Pérez, M A Martin, S Cañete, 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.Muscle & Nerve|March 1, 2002
Cosegregation of the mitochondrial DNA A1555G and G4309A mutations results in deafness and mitochondrial myopathyY Campos, A García, A López, et al.British Journal of Sports Medicine|July 26, 2006
Exercise capacity in a 78 year old patient with McArdle's disease: it is never too late to start exercisingM Perez, M A Martin, J C Rubio, et al.Science (New York, N.Y.)|June 14, 2014
Neuronal repair. Asynchronous therapy restores motor control by rewiring of the rat corticospinal tract after strokeA S Wahl, W Omlor, J C Rubio, et al.Muscle & Nerve|September 5, 2002
Molecular analysis of the superoxide dismutase 1 gene in Spanish patients with sporadic or familial amyotrophic lateral sclerosisA García-Redondo, F Bustos, B Juan Y Seva, et al.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.Neuromuscular Disorders : NMD|March 27, 1999
Clinical heterogeneity associated with mitochondrial DNA depletion in muscleY Campos, M A Martín, T García-Silva, et al.Pageof 5