BEGOÑA
ATARES PUEYO
Publications (18) Publications de BEGOÑA ATARES PUEYO
2017
2016
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Molecularly determined total tumour load in lymph nodes of stage I–II colon cancer patients correlates with high-risk factors. A multicentre prospective study
Virchows Archiv, Vol. 469, Núm. 4, pp. 385-394
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
2012
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Coexistence of protease sensitive and resistant prion protein in 129VV homozygous sporadic Creutzfeldt-Jakob disease: A case report
Journal of Medical Case Reports, Vol. 6
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Técnica del ganglio centinela en el cáncer de colon
Gaceta médica de Bilbao: Revista oficial de la Academia de Ciencias Médicas de Bilbao. Información para profesionales sanitarios, Vol. 109, Núm. 4, pp. 135-141
2010
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A Novel PRNP Y218N mutation in gerstmann-sträussler-scheinker disease with neurofibrillary degeneration
Journal of Neuropathology and Experimental Neurology, Vol. 69, Núm. 8, pp. 789-800
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A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report.
BMC neurology, Vol. 10, pp. 99
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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
2007
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Las encefalopatías espongiformes o enfermedades por priones en el País Vasco
Gaceta médica de Bilbao: Revista oficial de la Academia de Ciencias Médicas de Bilbao. Información para profesionales sanitarios, Vol. 104, Núm. 2, pp. 64-69
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
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Value of limited necropsy in HIV-positive patients
Pathology Research and Practice, Vol. 197, Núm. 3, pp. 165-168