Publicacións en colaboración con investigadores/as de Complexo Hospitalario Universitario de Santiago (6)

2016

  1. Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene

    Brain and Development, Vol. 38, Núm. 1, pp. 167-172

  2. Erratum: Corrigendum to “Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene” (Brain and Development (2016) 38(1) (167–172) (S0387760415001023) (10.1016/j.braindev.2015.05.008))

    Brain and Development

2014

  1. Exome sequencing identifies a CHKB mutation in Spanish patient with Megaconial Congenital Muscular Dystrophy and mtDNA depletion

    European Journal of Paediatric Neurology, Vol. 18, Núm. 6, pp. 796-800

  2. Increased lymphangiogenesis in Riedel thyroiditis (Immunoglobulin G4-related thyroid disease).

    Virchows Archiv : an international journal of pathology, Vol. 465, Núm. 3, pp. 359-364

2002

  1. Melanocitosis dérmica tardía

    Actas Dermo-Sifiliograficas, Vol. 93, Núm. 3, pp. 175-177

2000

  1. Neuropatia hereditaria con paralisis sensible a la presion (neuropatia tomacular). Estudio clinico, electrofisiologico y molecular de dos familias afectadas

    Revista de Neurologia, Vol. 31, Núm. 6, pp. 506-510