Publicaciones en colaboración con investigadores/as de Hospital Infantil Universitario Niño Jesus de Madrid (5)

2007

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

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

2006

  1. Mobilisation of mesenchymal cells into blood in response to skeletal muscle injury

    British Journal of Sports Medicine, Vol. 40, Núm. 8, pp. 719-722

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

1998

  1. Clinical heterogeneity associated with mitochondrial DNA depletion in muscle

    Neuromuscular Disorders, Vol. 8, Núm. 8, pp. 568-573

1997

  1. Leigh syndrome associated with the T9176C mutation in the ATPase 6 gene of mitochondrial DNA

    Neurology, Vol. 49, Núm. 2, pp. 595-597