Publicaciones en colaboración con investigadores/as de Universidad del País Vasco/Euskal Herriko Unibertsitatea (10)

2013

  1. A novel form of human disease

    Prion Biology: Research and Advances (Apple Academic Press), pp. 179-210

  2. Técnica del ganglio centinela en el cáncer de colon. Experiencia en 125 casos

    Cirugia Espanola, Vol. 91, Núm. 6, pp. 366-371

2010

  1. Somatic mosaicism in a case of apparently sporadic Creutzfeldt-Jakob disease carrying a de novo D178N mutation in the PRNP gene

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 153, Núm. 7, pp. 1283-1291

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. Familial prion diseases in the basque country (Spain)

    Neuroepidemiology, Vol. 24, Núm. 1-2, pp. 103-109

  3. 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