Universitat de Barcelona-ko ikertzaileekin lankidetzan egindako argitalpenak (5)

2023

  1. Expanding the phenotypic spectrum of TRAPPC11-related muscular dystrophy: 25 Roma individuals carrying a founder variant

    Journal of medical genetics, Vol. 60, Núm. 10, pp. 965-973

2022

  1. Impact of COVID-19 in Immunosuppressed Children With Neuroimmunologic Disorders

    Neurology(R) neuroimmunology & neuroinflammation, Vol. 9, Núm. 1

2020

  1. Associations of paediatric demyelinating and encephalitic syndromes with myelin oligodendrocyte glycoprotein antibodies: a multicentre observational study

    The Lancet Neurology, Vol. 19, Núm. 3, pp. 234-246

2017

  1. Distribution and genotype-phenotype correlation of GDAP1 mutations in Spain

    Scientific Reports, Vol. 7, Núm. 1

2016

  1. Myorhythmia-Like Dyskinesia Affecting the Face and Ear Associated With Anti–N-Methyl-d-Aspartate Receptor Encephalitis

    Movement Disorders Clinical Practice