Publications en collaboration avec des chercheurs de Hospital Universitario Araba (19)

2023

  1. Experiences of water immersion during childbirth: a qualitative thematic synthesis

    BMC Pregnancy and Childbirth, Vol. 23, Núm. 1

2019

  1. 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

  1. 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

  2. Sporadic Creutzfeldt–Jakob disease with glial PrPRes nuclear and perinuclear immunoreactivity

    Neuropathology, Vol. 38, Núm. 5, pp. 561-567

2017

  1. 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

  1. Type-2 diabetes primary prevention program implemented in routine primary care: A process evaluation study

    Trials, Vol. 17, Núm. 1

2015

  1. Coexistence of mixed phenotype Creutzfeldt-Jakob disease, Lewy body disease and argyrophilic grain disease plus histological features of possible Alzheimer's disease: A multi-protein disorder in an autopsy case

    Neuropathology, Vol. 35, Núm. 1, pp. 56-63

2014

  1. Online training course on critical appraisal for nurses: Adaptation and assessment

    BMC Medical Education, Vol. 14, Núm. 1

2013

  1. Oestrogen receptor polymorphisms are an associated risk factor for mild cognitive impairment and Alzheimer disease in women APOE ε4 carriers: A case-control study

    BMJ Open, Vol. 3, Núm. 9

2012

  1. 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

  2. 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

  1. 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

  2. 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

  3. 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

  1. Clinical characterization of a girl with trisomy 20q13.2qter and monosomy 13q33.1qter: Delineating phenotype-genotype correlations

    American Journal of Medical Genetics, Part A

  2. 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

  1. 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

  1. Combined Functional and Positional Gene Information for the Identification of Susceptibility Variants in Celiac Disease

    Gastroenterology, Vol. 134, Núm. 3, pp. 738-746

2004

  1. MICA response to gliadin in intestinal mucosa from celiac patients

    Immunogenetics, Vol. 56, Núm. 8, pp. 549-554