Publications in collaboration with researchers from Radboud University Nijmegen Medical Centre (9)

2021

  1. Author Correction: Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications (Scientific Reports, (2021), 11, 1, (1526), 10.1038/s41598-021-81093-y)

    Scientific Reports

  2. Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications

    Scientific Reports, Vol. 11, Núm. 1

  3. Impact of Bacillus Calmette-Gue´rin (BCG) vaccination on postoperative mortality in patients with perioperative SARS-CoV-2 infection

    BJS Open

  4. Machine learning risk prediction of mortality for patients undergoing surgery with perioperative SARS-CoV-2: The COVIDSurg mortality score

    British Journal of Surgery, Vol. 19, Núm. 4

2015

  1. How to match the optimal currently available inhaler device to an individual child with asthma or recurrent wheeze

    npj Primary Care Respiratory Medicine, Vol. 25

2014

  1. Classification and pharmacological treatment of preschool wheezing: Changes since 2008

    European Respiratory Journal

  2. Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance

    Human Molecular Genetics, Vol. 23, Núm. 11, pp. 2888-2900

2010

  1. Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia

    Human Mutation, Vol. 31, Núm. 8

2008

  1. Definition, assessment and treatment of wheezing disorders in preschool children: An evidence-based approach

    European Respiratory Journal, Vol. 32, Núm. 4, pp. 1096-1110