BEGOÑA
ATARES PUEYO
Universidad del País Vasco/Euskal Herriko Unibertsitatea
Lejona, EspañaPublications en collaboration avec des chercheurs de Universidad del País Vasco/Euskal Herriko Unibertsitatea (10)
2013
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A novel form of human disease
Prion Biology: Research and Advances (Apple Academic Press), pp. 179-210
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Técnica del ganglio centinela en el cáncer de colon. Experiencia en 125 casos
Cirugia Espanola, Vol. 91, Núm. 6, pp. 366-371
2010
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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
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Tau-predominant-associated pathology in a sporadic-late-onset Hallervorden-Spatz syndrome
Movement Disorders, Vol. 21, Núm. 1, pp. 107-111
2005
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A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease
Neurology, Vol. 64, Núm. 9, pp. 1578-1585
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Familial prion diseases in the basque country (Spain)
Neuroepidemiology, Vol. 24, Núm. 1-2, pp. 103-109
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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
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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
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The New Mutation, E46K, of α-Synuclein Causes Parkinson and Lewy Body Dementia
Annals of Neurology, Vol. 55, Núm. 2, pp. 164-173
2001
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Dementia, amyotrophy, and periodic complexes on the electroencephalogram: A diagnostic challenge
Archives of Neurology, Vol. 58, Núm. 10, pp. 1669-1672