Publicaciones en colaboración con investigadoras/es de Hospital Universitario Araba (17)

2024

  1. Association of retinal neurodegeneration with the progression of cognitive decline in Parkinson’s disease

    npj Parkinson's Disease, Vol. 10, Núm. 1

2019

  1. Long-term impact of subthalamic stimulation on cognitive function in patients with advanced Parkinson's disease

    Neurologia, Vol. 34, Núm. 9, pp. 573-581

2016

  1. One-year clinical experience of perampanel in Spain: A multicentre study of efficacy and tolerability

    Epileptic Disorders, Vol. 18, Núm. 2, pp. 173-180

  2. Síntomas no motores y motores en la enfermedad de Parkinson y su relación con la calidad de vida y los distintos subgrupos clínicos

    Neurologia, Vol. 31, Núm. 9, pp. 585-591

2015

  1. Autonomic involvement in Parkinsonian carriers of PARK2 gene mutations

    Parkinsonism and Related Disorders, Vol. 21, Núm. 7, pp. 717-722

  2. Cognitive and behavioral symptoms in Parkinson's disease patients with the G2019S and R1441G mutations of the LRRK2 gene

    Parkinsonism and Related Disorders, Vol. 21, Núm. 5, pp. 494-499

2014

  1. Impulse control and repetitive behaviors in Parkinson's disease - Are there differences in the relation to dopamine agonist treatment?

    Journal of the Neurological Sciences

2013

  1. Autonomic dysfunction in parkinsonian LRRK2 mutation carriers

    Parkinsonism and Related Disorders, Vol. 19, Núm. 10, pp. 906-909

  2. Cardiac sympathetic denervation in symptomatic and asymptomatic carriers of the E46K mutation in the α synuclein gene

    Parkinsonism and Related Disorders, Vol. 19, Núm. 1, pp. 95-100

  3. Nocturnal hypertension and dysautonomia in patients with Parkinson's disease: Are they related?

    Journal of Neurology, Vol. 260, Núm. 7, pp. 1752-1756

  4. The applause sign and neuropsychological profile in progressive supranuclear palsy and Parkinson's disease

    Clinical Neurology and Neurosurgery, Vol. 115, Núm. 8, pp. 1230-1233

2006

  1. Tau-predominant-associated pathology in a sporadic-late-onset Hallervorden-Spatz syndrome

    Movement Disorders, Vol. 21, Núm. 1, pp. 107-111

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. Phenotypic variability in familial prion diseases due to the D178N mutation

    Journal of Neurology, Neurosurgery and Psychiatry, Vol. 76, Núm. 11, pp. 1491-1496

2004

  1. Parkinson's disease-like presentation of multiple system atrophy with poor response to STN stimulation: A clinicopathological case report

    Movement Disorders, Vol. 19, Núm. 8, pp. 973-977

  2. The New Mutation, E46K, of α-Synuclein Causes Parkinson and Lewy Body Dementia

    Annals of Neurology, Vol. 55, Núm. 2, pp. 164-173

2001

  1. Dementia, amyotrophy, and periodic complexes on the electroencephalogram: A diagnostic challenge

    Archives of Neurology, Vol. 58, Núm. 10, pp. 1669-1672