Publicaciones en colaboración con investigadores/as de Hospital Universitari de Bellvitge (11)

2024

  1. Delphi consensus on the transition from paediatric to adult epilepsy care

    Neurology Perspectives, Vol. 4, Núm. 2

2023

  1. Frequency and phenotypic spectrum of spinocerebellar ataxia 27B and other genetic ataxias in a Spanish cohort of late-onset cerebellar ataxia

    European Journal of Neurology, Vol. 30, Núm. 12, pp. 3828-3833

2022

  1. Melatonin in sleep disorders

    Neurologia, Vol. 37, Núm. 7, pp. 575-585

2021

  1. Relationship between sleep quality and cognitive performance in patients with epilepsy

    Epilepsy and Behavior, Vol. 122

2020

  1. Sleep-related movement and behavioural disorders in adults

    Revista de Neurologia, Vol. 71, Núm. 10, pp. 377-386

  2. Targeted next-generation sequencing in a large cohort of genetically undiagnosed patients with neuromuscular disorders in Spain

    Genes, Vol. 11, Núm. 5

2019

  1. Actininopathy: A new muscular dystrophy caused by ACTN2 dominant mutations

    Annals of Neurology, Vol. 85, Núm. 6, pp. 899-906

2017

  1. EARLY-ESLI study: Long-term experience with eslicarbazepine acetate after first monotherapy failure

    Acta Neurologica Scandinavica, Vol. 136, Núm. 3, pp. 254-264

2016

  1. Muscle imaging in muscle dystrophies produced by mutations in the EMD and LMNA genes

    Neuromuscular Disorders, Vol. 26, Núm. 1, pp. 33-40

2011

  1. Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathy

    Neuromuscular Disorders, Vol. 21, Núm. 8, pp. 533-542

2008

  1. Mutations in Progranulin Gene: Clinical, Pathological, and Ribonucleic Acid Expression Findings

    Biological Psychiatry, Vol. 63, Núm. 10, pp. 946-952