Pediatría
Servizo
University of Amsterdam
Ámsterdam, HolandaPublicacións en colaboración con investigadores/as de University of Amsterdam (21)
2024
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External validation of a multivariable prediction model for identification of pneumonia and other serious bacterial infections in febrile immunocompromised children
Archives of Disease in Childhood, Vol. 109, Núm. 1, pp. 58-66
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Plasma Protein Biomarkers Distinguish Multisystem Inflammatory Syndrome in Children From Other Pediatric Infectious and Inflammatory Diseases
The Pediatric infectious disease journal, Vol. 43, Núm. 5, pp. 444-453
2023
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Adeno-associated virus 2 infection in children with non-A–E hepatitis
Nature, Vol. 617, Núm. 7961, pp. 555-563
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Diagnosis of childhood febrile illness using a multi-class blood RNA molecular signature
Med, Vol. 4, Núm. 9, pp. 635-654.e5
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Economic burden and health-related quality-of-life among infants with respiratory syncytial virus infection: A multi-country prospective cohort study in Europe
Vaccine, Vol. 41, Núm. 16, pp. 2707-2715
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Genomic investigations of unexplained acute hepatitis in children
Nature, Vol. 617, Núm. 7961, pp. 564-573
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Relationship between molecular pathogen detection and clinical disease in febrile children across Europe: a multicentre, prospective observational study
The Lancet Regional Health - Europe, Vol. 32
2022
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Hemostasis Proteins in Invasive Meningococcal and Nonmeningococcal Infections: A Prospective Multicenter Study
Pediatric Critical Care Medicine, Vol. 23, Núm. 12, pp. E543-E554
2021
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A Novel Framework for Phenotyping Children With Suspected or Confirmed Infection for Future Biomarker Studies
Frontiers in Pediatrics, Vol. 9
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A generic emergency protocol for patients with inborn errors of metabolism causing fasting intolerance: A retrospective, single-center study and the generation of www.emergencyprotocol.net
Journal of Inherited Metabolic Disease, Vol. 44, Núm. 5, pp. 1124-1135
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Galactokinase deficiency: lessons from the GalNet registry
Genetics in Medicine, Vol. 23, Núm. 1, pp. 202-210
2020
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Biomarkers for the Discrimination of Acute Kawasaki Disease From Infections in Childhood
Frontiers in Pediatrics, Vol. 8
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Whole-exome sequencing for the identification of rare variants in primary immunodeficiency genes in children with sepsis: A prospective, population-based cohort study
Clinical Infectious Diseases, Vol. 71, Núm. 10, pp. E614-E623
2019
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Identification of regulatory variants associated with genetic susceptibility to meningococcal disease
Scientific Reports, Vol. 9, Núm. 1
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Plasma lipid profiles discriminate bacterial from viral infection in febrile children
Scientific Reports, Vol. 9, Núm. 1
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The natural history of classic galactosemia: Lessons from the GalNet registry
Orphanet Journal of Rare Diseases, Vol. 14, Núm. 1
2016
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Diagnostic test accuracy of a 2-transcript host RNA signature for discriminating bacterial vs viral infection in febrile children
JAMA - Journal of the American Medical Association, Vol. 316, Núm. 8, pp. 835-845
2013
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Long-term follow-up and outcome of phenylketonuria patients on sapropterin: A retrospective study
Pediatrics, Vol. 131, Núm. 6
2012
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Diversity of approaches to classic galactosemia around the world: A comparison of diagnosis, intervention, and outcomes
Journal of Inherited Metabolic Disease, Vol. 35, Núm. 6, pp. 1037-1049
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Erratum: Diversity of approaches to classic galactosemia around the world: A comparison of diagnosis, intervention, and outcomes (J Inherit Metab Dis DOI 10.1007/s10545-012-9477-y)
Journal of Inherited Metabolic Disease