Publicaciones en las que colabora con José Felix Martí Massó (33)

2018

  1. Familial amyloidosis with polyneuropathy type 1 caused by transthyretin mutation Val50Met (Val30Met): 4 cases in a non-endemic area

    Neurologia, Vol. 33, Núm. 9, pp. 583-589

2013

  1. The ACMSD gene, involved in tryptophan metabolism, is mutated in a family with cortical myoclonus, epilepsy, and parkinsonism

    Journal of Molecular Medicine, Vol. 91, Núm. 12, pp. 1399-1406

2011

  1. Olfactory deficits and cardiac 123I-MIBG in Parkinson's disease related to the LRRK2 R1441G and G2019S mutations

    Movement Disorders, Vol. 26, Núm. 11, pp. 2026-2031

2006

  1. A retrospective study comparing two formulations of valproic acid

    Revista de Neurologia, Vol. 42, Núm. 3, pp. 129-132

  2. Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy

    Epilepsy Research, Vol. 70, Núm. 2-3, pp. 118-126

  3. Pérdida completa de ensoñaciones tras una lesión cerebral temporooccipital izquierda

    Neurologia, Vol. 21, Núm. 3, pp. 152-154

2005

  1. Análisis de la marcha en la enfermedad de Parkinson y su respuesta al tratamiento dopaminérgico

    Medicina Clinica, Vol. 124, Núm. 2, pp. 50-52

  2. Análisis de la marcha y del movimiento de las extremidades superiores en distrofias musculares

    Neurologia, Vol. 20, Núm. 7, pp. 341-348

  3. LGMD2A: Genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene

    Brain, Vol. 128, Núm. 4, pp. 732-742

  4. Trimetazidine induces parkinsonism, gait disorders and tremor

    Therapie

2004

  1. Prevalence of Parkinson's disease and other types of Parkinsonism: A door-to-door survey in Bidasoa, Spain

    Journal of Neurology, Vol. 251, Núm. 3, pp. 340-345

2002

  1. Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy

    Human Molecular Genetics, Vol. 11, Núm. 9, pp. 1119-1128

2001

  1. Prevalence of essential tremor: A door-to-door survey in Bidasoa, Spain

    Neuroepidemiology, Vol. 20, Núm. 2, pp. 125-128

  2. The validity of Hodkinson's Abbreviated Mental Test for dementia screening in Guipuzcoa, Spain

    European Journal of Neurology, Vol. 8, Núm. 5, pp. 435-440

2000

  1. Sindrome de apnea del sueno e infarto cerebral

    Neurologia, Vol. 15, Núm. 1, pp. 3-7

  2. Síndrome de Andersen. Descripción de un caso

    Neurologia, Vol. 15, Núm. 8, pp. 366-369

1999

  1. Autosomal dominant lateral temporal epilepsy: Clinical and genetic study of a large Basque pedigree linked to chromosome 10q

    Annals of Neurology, Vol. 45, Núm. 2, pp. 182-188

  2. Cinnarizine-induced parkinsonism: Ten years later (multiple letters) [1]

    Movement Disorders

1998

  1. Cinnarizine-induced parkinsonism: Ten years later

    Movement Disorders, Vol. 13, Núm. 3, pp. 453-456

  2. Limb-girdle muscular dystrophy in Guipuzcoa (Basque Country, Spain)

    Brain, Vol. 121, Núm. 9, pp. 1735-1747