Publicaciones en colaboración con investigadores/as de Consejo Superior de Investigaciones Científicas (5)

2007

  1. X-linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy

    Annals of Neurology, Vol. 61, Núm. 1, pp. 73-83

2005

  1. Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 gene

    Archives of Neurology, Vol. 62, Núm. 4, pp. 659-661

2003

  1. Myoglobinuria and COX deficiency in a patient taking cerivastatin and gemfibrozil

    Neurology, Vol. 60, Núm. 1, pp. 124-126

1997

  1. Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria

    Pediatric Neurology, Vol. 17, Núm. 2, pp. 165-170

1994

  1. Effects of l-carnitine on the pyruvate dehydrogenase complex and carnitine palmitoyl transferase activities in muscle of endurance athletes

    FEBS Letters, Vol. 341, Núm. 1, pp. 91-93