Publicaciones en colaboración con investigadoras/es de Hospital Universitari de Bellvitge (4)

2019

  1. A unique common ancestor introduced P301L mutation in MAPT gene in frontotemporal dementia patients from Barcelona (Baix Llobregat, Spain)

    Neurobiology of Aging, Vol. 84, pp. 236.e9-236.e15

2017

  1. Frontotemporal Dementia Caused by the P301L Mutation in the MAPT Gene: Clinicopathological Features of 13 Cases from the Same Geographical Origin in Barcelona, Spain

    Dementia and Geriatric Cognitive Disorders, Vol. 44, Núm. 3-4, pp. 213-221

2013

  1. A novel form of human disease

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

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