Publikationen in Zusammenarbeit mit Forschern von Hospital Universitari de Bellvitge (4)

2022

  1. Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias

    International Journal of Molecular Sciences, Vol. 23, Núm. 19

2019

  1. The Role of Factor V Leiden, Prothrombin G20210A, and MTHFR C677T Mutations in Neonatal Cerebral Sinovenous Thrombosis

    Clinical and Applied Thrombosis/Hemostasis, Vol. 25

2017

  1. Molecular characterization of congenital myasthenic syndromes in Spain

    Neuromuscular Disorders, Vol. 27, Núm. 12, pp. 1087-1098

  2. Myths and evidence on the use of botulinum toxin: Spasticity in adults and in children with cerebral palsy

    Revista de Neurologia, Vol. 64, Núm. 10, pp. 459-470