Publikationen in Zusammenarbeit mit Forschern von Hospital General Universitario Gregorio Marañón (19)

2024

  1. Haemoglobinopathies and other rare anemias in Spain: ten years of a nationwide registry (REHem-AR)

    Annals of Hematology, Vol. 103, Núm. 8, pp. 2743-2755

  2. Pulmonary function and bronchopulmonary dysplasia classification: insights from the Spanish Registry

    European Journal of Pediatrics, Vol. 183, Núm. 9, pp. 3757-3766

2023

  1. Immunisation schedule of the Spanish Association of Paediatrics: 2023 Recommendations

    Anales de Pediatria, Vol. 98, Núm. 1, pp. 58.e1-58.e10

2022

  1. Immunisation schedule of the Pediatric Spanish Association: 2022 recommendations

    Anales de Pediatria, Vol. 96, Núm. 1, pp. 59.e1-59.e10

  2. Incidence and Prevalence of Children's Diffuse Lung Disease in Spain

    Archivos de Bronconeumologia, Vol. 58, Núm. 1, pp. 22-29

  3. Lung Ultrasound Scores Progress Differently in Extreme and Very Preterm Infants after Birth: A Multicentre Prospective Study

    Neonatology, Vol. 119, Núm. 5, pp. 558-566

  4. Neuroblastoma in Spain: Linking the national clinical database and epidemiological registries – A study by the Joint Action on Rare Cancers

    Cancer Epidemiology, Vol. 78

  5. Usefulness of lung ultrasound in the diagnosis and follow-up of respiratory diseases in neonates

    Anales de Pediatria, Vol. 96, Núm. 3, pp. 252.e1-252.e13

2021

  1. Author Correction: The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome (Scientific Reports, (2017), 7, 1, (12288), 10.1038/s41598-017-11620-3)

    Scientific Reports

  2. Immunisation schedule of the Pediatric Spanish Association: 2021 recommendations

    Anales de Pediatria, Vol. 94, Núm. 1, pp. 53.e1-53.e10

2020

  1. Immunisation schedule of the Spanish Association of Paediatrics: 2020 recommendations

    Anales de Pediatria, Vol. 92, Núm. 1, pp. 52.e1-52.e10

  2. Update of the Spanish registry of haemoglobinopathies in children and adults

    Medicina Clinica, Vol. 155, Núm. 3, pp. 95-103

2019

  1. Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism

    Movement Disorders, Vol. 34, Núm. 10, pp. 1547-1561

  2. Reply to: “Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion”

    Movement Disorders

  3. X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients

    Scientific Reports, Vol. 9, Núm. 1

2017

  1. The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome

    Scientific Reports, Vol. 7, Núm. 1

2016

  1. Impact of quality-indicator-based measures to improve the treatment of acute poisoning in pediatric emergency patients

    Emergencias, Vol. 28, Núm. 1, pp. 31-37

2010

  1. Occult pneumonia in infants with high fever without source: A prospective multicenter study

    Pediatric Emergency Care, Vol. 26, Núm. 7, pp. 470-474

2006

  1. Emergency visits for childhood poisoning: A 2-year prospective multicenter survey in Spain

    Pediatric Emergency Care, Vol. 22, Núm. 5, pp. 334-338