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Revista De Neurologia|November 12, 1998
[Enzyme complex defects of the mitochondrial respiratory chain]J C Rubio, M A Martín, P del Hoyo, et al.Annals of Neurology|March 20, 1998
Complex I defect in muscle from patients with Huntington's diseaseJ Arenas, Y Campos, R Ribacoba, et al.Revista De Neurologia|November 12, 1998
[Molecular genetics of alterations in the mitochondrial respiratory chain]M A Martín, Y Campos, F de Bustos, et al.Neuromuscular Disorders : NMD|June 26, 1999
McArdle's disease associated with homozygosity for the missense mutation Gly204Ser of the myophosphorylase gene in a Spanish patientJ C Rubio, M A Martín, A García, et al.Biochemical and Biophysical Research Communications|September 23, 1997
Bilateral striatal necrosis and MELAS associated with a new T3308C mutation in the mitochondrial ND1 geneY Campos, M A Martín, J C Rubio, et al.Neuromuscular Disorders : NMD|March 11, 2000
Single large-scale mitochondrial DNA deletion in a patient with encephalopathy, cardiomyopathy, and prominent intestinal pseudo-obstructionY Campos, M A Martín, C Caballero, et al.Neurology|November 26, 2003
Splicing mosaic of the myophosphorylase gene due to a silent mutation in McArdle diseaseI Fernandez-Cadenas, A L Andreu, J Gamez, et al.Journal of the Neurological Sciences|January 8, 1999
Myophosphorylase deficiency associated with a defect in complex I of the mitochondrial respiratory chainJ C Rubio, M A Martín, J Bautista, et al.Neurology|August 1, 1997
Leigh syndrome associated with the T9176C mutation in the ATPase 6 gene of mitochondrial DNAY Campos, M A Martín, J C Rubio, et al.British Journal of Sports Medicine|March 1, 2006
C34T mutation of the AMPD1 gene in an elite white runnerA Lucia, M A Martin, J Esteve-Lanao, et al.Pageof 5