Publicaciones en colaboración con investigadores/as de Hospital Universitario Araba (13)

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

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

2001

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

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

  2. Value of limited necropsy in HIV-positive patients

    Pathology Research and Practice, Vol. 197, Núm. 3, pp. 165-168