MEDICINA MOLECULAR
Complexo Hospitalario Universitario de Santiago
Santiago de Compostela, EspañaPublications in collaboration with researchers from Complexo Hospitalario Universitario de Santiago (11)
2024
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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
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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
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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
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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
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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
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A single nucleotide polymorphism in the RASGRF2 gene is associated with alcoholic liver cirrhosis in men
PLoS ONE, Vol. 11, Núm. 12
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Alcoholic liver disease and hepatitis C virus infection
World journal of gastroenterology, Vol. 22, Núm. 4, pp. 1411-1420
2012
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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
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The human Tp53 Arg72Pro polymorphism explains different functional prognosis in stroke
Journal of Experimental Medicine, Vol. 208, Núm. 3, pp. 429-437
2006
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Genomic rearrangements at the BRCA1 locus in Spanish families with breast/ovarian cancer
Clinical Chemistry, Vol. 52, Núm. 8, pp. 1480-1485
2004
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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