Publicaciones en colaboración con investigadores/as de Complexo Hospitalario Universitario de Santiago (16)

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

2021

  1. 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

  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. 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

  2. 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

  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

2014

  1. 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

  1. Optimal management of breakthrough cancer pain (BCP)

    Clinical and Translational Oncology, Vol. 15, Núm. 7, pp. 526-534

  2. 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

  1. Breakthrough cancer pain - Still a challenge

    Journal of Pain Research, Vol. 5, pp. 559-566

  2. 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