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Neuromuscular Disorders : NMD|September 21, 2000
A mitochondrial tRNA(Lys) gene mutation (T8316C) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodesY Campos, G Lorenzo, M A Martín, et al.
Biomedical Materials (Bristol, England)|April 18, 2015
Fracture bone healing and biodegradation of AZ31 implant in ratsC Iglesias, O G Bodelón, R Montoya, et al.
Clinical Genetics|February 13, 2001
Resolution of a mispaired secondary structure intermediate could account for a novel micro-insertion/deletion (387 insA/del 8 bp) in the PYGM gene causing McArdle's diseaseM A Martín, J C Rubio, A García, et al.
Biochimica Et Biophysica Acta|November 9, 2000
Myocardial carnitine and carnitine palmitoyltransferase deficiencies in patients with severe heart failureM A Martín, M A Gómez, F Guillén, et al.
Muscle & Nerve|July 9, 1999
Molecular analysis in Spanish patients with muscle carnitine palmitoyltransferase deficiencyM A Martín, J C Rubio, F De Bustos, et al.
Human Mutation|June 22, 2000
Identification of novel mutations in Spanish patients with muscle carnitine palmitoyltransferase II deficiencyM A Martín, J C Rubio, P del Hoyo, et al.
Neurology|February 5, 1999
A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibersJ Arenas, Y Campos, B Bornstein, et al.
British Journal of Sports Medicine|September 27, 2006
Can patients with McArdle's disease run?M Pérez, M Moran, C Cardona, et al.
Muscle & Nerve|August 3, 2000
Molecular analysis of Spanish patients with AMP deaminase deficiencyJ C Rubio, M A Martín, P Del Hoyo, et al.
Revista De Neurologia|September 19, 2007
[Private mutations in the myophosphorylase gene: the first case in a patient of Latin American descent]I Fernandez-Cadenas, G Nogales-Gadea, D Llige, et al.
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