Bioef
Research center
Hospital Universitario Araba
Vitoria, EspañaPublications in collaboration with researchers from Hospital Universitario Araba (19)
2023
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Experiences of water immersion during childbirth: a qualitative thematic synthesis
BMC Pregnancy and Childbirth, Vol. 23, Núm. 1
2019
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The consequences of implementing non-invasive prenatal testing with cell-free foetal DNA for the detection of Down syndrome in the Spanish National Health Service: A cost-effectiveness analysis
Cost Effectiveness and Resource Allocation, Vol. 17, Núm. 1
2018
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Brains with sporadic Creutzfeldt-Jakob disease and copathology showed a prolonged end-stage of disease
Journal of Clinical Pathology, Vol. 71, Núm. 5, pp. 446-450
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Sporadic Creutzfeldt–Jakob disease with glial PrPRes nuclear and perinuclear immunoreactivity
Neuropathology, Vol. 38, Núm. 5, pp. 561-567
2017
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Upregulated Expression of Heparanase and Heparanase 2 in the Brains of Alzheimer's Disease
Journal of Alzheimer's Disease, Vol. 58, Núm. 1, pp. 185-192
2016
2015
2014
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Online training course on critical appraisal for nurses: Adaptation and assessment
BMC Medical Education, Vol. 14, Núm. 1
2013
2012
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Novel mutations in MEN1, CDKN1B and AIP genes in patients with multiple endocrine neoplasia type 1 syndrome in Spain
Clinical Endocrinology, Vol. 76, Núm. 5, pp. 719-724
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UBQ-8i polymorphism is not an independent risk factor for mild cognitive impairment and Alzheimer's disease in APOE-4 carriers
Current Alzheimer Research, Vol. 9, Núm. 4, pp. 467-472
2011
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Mitochondrial DNA analysis of formalin-fixed paraffin-embedded tissue samples: Effect of formalin on DNA stability and its implications in genetic studies
Forensic Science International: Genetics Supplement Series, Vol. 3, Núm. 1
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Perfiles genéticos de longevidad y envejecimiento saludable en nonagenarios del país vasco
Revista Espanola de Geriatria y Gerontologia, Vol. 46, Núm. 4, pp. 217-222
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Progression from amnesic mild cognitive impairment to alzheimer's disease: ESR1 and ESR2 polymorphisms and APOE gene
Dementia and Geriatric Cognitive Disorders, Vol. 32, Núm. 5, pp. 332-341
2010
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Clinical characterization of a girl with trisomy 20q13.2qter and monosomy 13q33.1qter: Delineating phenotype-genotype correlations
American Journal of Medical Genetics, Part A
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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
2009
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The COMT Val158 met polymorphism as an associated risk factor for Alzheimer disease and mild cognitive impairment in APOE 4 carriers
BMC Neuroscience, Vol. 10, pp. 125
2008
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Combined Functional and Positional Gene Information for the Identification of Susceptibility Variants in Celiac Disease
Gastroenterology, Vol. 134, Núm. 3, pp. 738-746
2004
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MICA response to gliadin in intestinal mucosa from celiac patients
Immunogenetics, Vol. 56, Núm. 8, pp. 549-554