Publicaciones en colaboración con investigadores/as de Hospital Universitario 12 de Octubre (3)

2020

  1. Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)

    Orphanet Journal of Rare Diseases, Vol. 15, Núm. 1

2017

  1. Genotypic and phenotypic features of all Spanish patients with McArdle disease: A 2016 update

    BMC Genomics, Vol. 18

2012

  1. Genotypic and phenotypic features of McArdle disease: Insights from the Spanish national registry

    Journal of Neurology, Neurosurgery and Psychiatry, Vol. 83, Núm. 3, pp. 322-328