Joaquín Arenas Barbero-rekin lankidetzan egindako argitalpenak (5)

2007

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

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

2006

  1. Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population

    Archives of Neurology, Vol. 63, Núm. 1, pp. 107-111

  2. Does the C34T mutation in AMPD1 alter exercise capacity in the elderly?

    International Journal of Sports Medicine, Vol. 27, Núm. 6, pp. 425-435

  3. 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