Microfluidics and Biomics Cluster UPV/EHU - GIC 21/107
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Hospital de Cruces
Barakaldo, EspañaPublications en collaboration avec des chercheurs de Hospital de Cruces (20)
2014
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Coregulation and modulation of NFκB-related genes in celiac disease: Uncovered aspects of gut mucosal inflammation
Human Molecular Genetics, Vol. 23, Núm. 5
2013
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A novel form of human disease
Prion Biology: Research and Advances (Apple Academic Press), pp. 179-210
2012
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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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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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Cardiac sympathetic denervation precedes nigrostriatal loss in the E46K mutation of the α-synuclein gene (SNCA)
Clinical Autonomic Research, Vol. 20, Núm. 4, pp. 267-269
2009
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Lrrk2 R1441G-related Parkinson's disease: Evidence of a common founding event in the seventh century in Northern Spain
Neurogenetics, Vol. 10, Núm. 4, pp. 347-353
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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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Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation
Neurogenetics, Vol. 9, Núm. 2, pp. 109-118
2007
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Lrrk2-associated parkinsonism is a major cause of disease in Northern Spain
Parkinsonism and Related Disorders, Vol. 13, Núm. 8, pp. 509-515
2006
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Fetal sex determination from maternal plasma by nested PCR of the amelogenin gene
International Congress Series, Vol. 1288, pp. 691-693
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Polymorphism in the cholesterol 24S-hydroxylase gene (CYP46A1) associated with the APOEε3 allele increases the risk of Alzheimer's disease and of mild cognitive impairment progressing to Alzheimer's disease
Dementia and Geriatric Cognitive Disorders, Vol. 21, Núm. 2, pp. 81-87
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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Ancestral origins of the prion protein gene D178N mutation in the Basque Country
Human Genetics, Vol. 117, Núm. 1, pp. 61-69
2004
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High levels of p53 protein expression do not correlate with p53 mutations in hepatocellular carcinoma
Journal of Viral Hepatitis, Vol. 11, Núm. 6, pp. 502-510
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Patterns of methylation profiles as diagnostic markers for multiple hepatocellular carcinomas
Scandinavian Journal of Gastroenterology, Vol. 39, Núm. 3, pp. 246-251
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p14ARF gene alterations in human hepatocellular carcinoma
European Journal of Gastroenterology and Hepatology, Vol. 16, Núm. 1, pp. 19-26
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p16INK4A Gene alterations are not a prognostic indicator for survival in patients with hepatocellular carcinoma undergoing curative hepatectomy
Journal of Gastroenterology and Hepatology (Australia), Vol. 19, Núm. 4, pp. 397-405
2003
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5-Hydroxytryptamine 6 receptor (5-HT6) receptor and apolipoprotein E (ApoE) polymorphisms in patients with Alzheimer's disease in the Basque Country
Neuroscience Letters, Vol. 339, Núm. 1, pp. 85-87
1996
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Effects of dexfenfluramine on weight loss and serum amino acids profile in obese subjects
Nutrition Research, Vol. 16, Núm. 10, pp. 1671-1678
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La «huella ADN» en lugar de la «huella plantar» en la identificación neonatal
Medicina Clinica, Vol. 107, Núm. 4, pp. 121-123