Publicaciones en las que colabora con Idoia Rouco Axpe (20)

2023

  1. Epidemiology of ataxia and hereditary spastic paraplegia in Spain: a cross-sectional study

    Neurologia, Vol. 38, Núm. 6, pp. 379-386

2022

  1. Neuropsychological Profile of Hereditary Ataxias: Study of 38 Patients

    Archives of Clinical Neuropsychology, Vol. 37, Núm. 5, pp. 904-915

2018

  1. Enfermedades degenerativas motoras y cerebelosas

    Neurología (Elsevier), pp. 569-582

  2. Trastornos motores

    Neurología (Elsevier), pp. 41-60

2016

  1. Manifestaciones neurológicas en la enfermedad de Erdheim-Chester: a propósito de 2 casos

    Neurologia

2015

  1. Enfermedad de Hirayama: ¿operar o no operar?

    Neurologia

  2. Experience with immunotherapy in 3 patients with cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies

    Neurologia

2014

  1. Sporadic hyperekplexia presenting with an ataxic gait

    Journal of Clinical Neuroscience, Vol. 21, Núm. 2, pp. 345-346

2011

  1. Impact of psychiatric symptoms and sleep disorders on the quality of life of patients with Parkinson's disease

    Journal of Neurology, Vol. 258, Núm. 3, pp. 494-499

2008

  1. Fluctuaciones motoras y discinesias en la enfermedad de Parkinson: Variables que discriminan ambas complicaciones en una muestra de 285 pacientes

    Neurologia, Vol. 23, Núm. 8, pp. 494-498

2007

  1. Influence of motor symptoms upon the quality of life of patients with Parkinson's disease

    European Neurology, Vol. 57, Núm. 3, pp. 161-165

  2. Restless legs syndrome in Parkinson's disease

    Movement Disorders, Vol. 22, Núm. 13, pp. 1912-1916

2006

  1. Sleep complaints and their relation with drug treatment in patients suffering from Parkinson's disease

    Movement Disorders, Vol. 21, Núm. 7, pp. 983-988

  2. Utilidad del estudio del sistema nervioso vegetativo en el diagnóstico diferencial entre la enfermedad de Parkinson y la atrofia multisistémica

    Neurologia, Vol. 21, Núm. 3, pp. 119-123

2005

  1. A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease

    Neurology, Vol. 64, Núm. 9, pp. 1578-1585

  2. Cerebrovascular disease in a tertiary care hospital. Current situation and issues to be improved

    Revista de Neurologia, Vol. 40, Núm. 12, pp. 723-728

  3. Use of ziprasidonein parkinsonian patients with psychosis

    Clinical Neuropharmacology, Vol. 28, Núm. 3, pp. 111-114

2003

  1. Post-transplantation HTLV-1 myelopathy in three recipients from a single donor

    Journal of Neurology Neurosurgery and Psychiatry, Vol. 74, Núm. 8, pp. 1080-1084

2001

  1. Human T lymphotropic virus type I (HTLV-1) associated myelopathy acquired through a liver transplant [2]

    Journal of Neurology Neurosurgery and Psychiatry

  2. Neuropatía óptica unilateral asociada a fistula arteriovenosa dural

    Neurologia, Vol. 16, Núm. 4, pp. 176-180