CANCIRMED
Complexo Hospitalario Universitario de Santiago
Santiago de Compostela, EspañaPublicacións en colaboración con investigadores/as de Complexo Hospitalario Universitario de Santiago (16)
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
2021
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Implementation of the Quality Oncology Practice Initiative Program in Spain: First Results and Implications
JCO oncology practice, Vol. 17, Núm. 8, pp. e1162-e1169
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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Clinical practice evaluation of opioids induced constipation management in oncologic patients: The EIO-50 project
Annals of oncology : official journal of the European Society for Medical Oncology, Vol. 29, pp. viii612
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The quality oncology practice initiative program: Experience in Spain
Annals of oncology : official journal of the European Society for Medical Oncology, Vol. 29, pp. viii570-viii571
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
2014
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Análisis de impacto presupuestario del uso de fentanilo intranasal en pectina para el tratamiento del dolor irruptivo oncológico
Pharmacoeconomics - Spanish Research Articles, Vol. 11, Núm. 2, pp. 51-60
2013
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Optimal management of breakthrough cancer pain (BCP)
Clinical and Translational Oncology, Vol. 15, Núm. 7, pp. 526-534
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Relationship between the pharmacokinetic properties and efficacy of fentanyl pectin nasal spray in breakthrough cancer pain
Atencion Farmaceutica, Vol. 15, Núm. 1, pp. 40-45
2012
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Breakthrough cancer pain - Still a challenge
Journal of Pain Research, Vol. 5, pp. 559-566
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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