PEDIATRÍA CLÍNICA Y ENFERMEDADES RARAS
Hospital General Universitario Gregorio Marañón
Madrid, EspañaPublicaciones en colaboración con investigadores/as de Hospital General Universitario Gregorio Marañón (19)
2024
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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
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Pulmonary function and bronchopulmonary dysplasia classification: insights from the Spanish Registry
European Journal of Pediatrics, Vol. 183, Núm. 9, pp. 3757-3766
2023
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Immunisation schedule of the Spanish Association of Paediatrics: 2023 Recommendations
Anales de Pediatria, Vol. 98, Núm. 1, pp. 58.e1-58.e10
2022
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Immunisation schedule of the Pediatric Spanish Association: 2022 recommendations
Anales de Pediatria, Vol. 96, Núm. 1, pp. 59.e1-59.e10
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Incidence and Prevalence of Children's Diffuse Lung Disease in Spain
Archivos de Bronconeumologia, Vol. 58, Núm. 1, pp. 22-29
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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
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Neuroblastoma in Spain: Linking the national clinical database and epidemiological registries – A study by the Joint Action on Rare Cancers
Cancer Epidemiology, Vol. 78
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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
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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
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Immunisation schedule of the Pediatric Spanish Association: 2021 recommendations
Anales de Pediatria, Vol. 94, Núm. 1, pp. 53.e1-53.e10
2020
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Immunisation schedule of the Spanish Association of Paediatrics: 2020 recommendations
Anales de Pediatria, Vol. 92, Núm. 1, pp. 52.e1-52.e10
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Update of the Spanish registry of haemoglobinopathies in children and adults
Medicina Clinica, Vol. 155, Núm. 3, pp. 95-103
2019
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Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism
Movement Disorders, Vol. 34, Núm. 10, pp. 1547-1561
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Reply to: “Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion”
Movement Disorders
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X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients
Scientific Reports, Vol. 9, Núm. 1
2017
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The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome
Scientific Reports, Vol. 7, Núm. 1
2016
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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
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Occult pneumonia in infants with high fever without source: A prospective multicenter study
Pediatric Emergency Care, Vol. 26, Núm. 7, pp. 470-474
2006
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Emergency visits for childhood poisoning: A 2-year prospective multicenter survey in Spain
Pediatric Emergency Care, Vol. 22, Núm. 5, pp. 334-338