Complexo Hospitalario Universitario de Santiago-ko ikertzaileekin lankidetzan egindako argitalpenak (11)

2024

  1. Consenso del grupo de trabajo de los trastornos de la conducta alimentaria de SENPE (GTTCA-SENPE). Evaluación y tratamiento médico-nutricional en la anorexia nerviosa. Actualización 2023

    Nutricion hospitalaria, Vol. 41, Núm. 1, pp. 1-60

2022

  1. Genetic susceptibility to telomere shortening through the rs2293607 polymorphism is associated with a greater risk of alcohol use disorder

    Mechanisms of ageing and development, Vol. 206, pp. 111693

2020

  1. The impact of vascular burden on behavioural and psychological symptoms in older adults with dementia: the BEVASDE study

    Neurological Sciences, Vol. 41, Núm. 1, pp. 165-174

2018

  1. Consenso sobre la evaluación y el tratamiento nutricional de los trastornos de la conducta alimentaria: Anorexia nerviosa, bulimia nerviosa, trastorno por atracón y otros. resumen ejecutivo

    Nutricion Hospitalaria, Vol. 35, Núm. 2, pp. 489-494

2017

  1. Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

    Nature Genetics, Vol. 49, Núm. 7, pp. 993-1004

2016

  1. A single nucleotide polymorphism in the RASGRF2 gene is associated with alcoholic liver cirrhosis in men

    PLoS ONE, Vol. 11, Núm. 12

  2. Alcoholic liver disease and hepatitis C virus infection

    World journal of gastroenterology, Vol. 22, Núm. 4, pp. 1411-1420

2012

  1. Prevalence of autosomal recessive congenital ichthyosis: A population-based study using the capture-recapture method in Spain

    Journal of the American Academy of Dermatology, Vol. 67, Núm. 2, pp. 240-244

2011

  1. The human Tp53 Arg72Pro polymorphism explains different functional prognosis in stroke

    Journal of Experimental Medicine, Vol. 208, Núm. 3, pp. 429-437

2006

  1. Genomic rearrangements at the BRCA1 locus in Spanish families with breast/ovarian cancer

    Clinical Chemistry, Vol. 52, Núm. 8, pp. 1480-1485

2004

  1. The variant E233G of the rad51d gene could be a low-penetrance allele in high-risk breast cancer families without BRCA1/2 mutations

    International Journal of Cancer, Vol. 110, Núm. 6, pp. 845-849