Grupo de Investigación de Endocrinología, Diabetes, Nutrición, alteraciones Renales y Salud Infantil - GIC 21/144
Hospital Infantil Universitario Niño Jesus de Madrid
Madrid, EspañaPublicaciones en colaboración con investigadoras/es de Hospital Infantil Universitario Niño Jesus de Madrid (31)
2023
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Correction: Vitamin C and folate status in hereditary fructose intolerance (European Journal of Clinical Nutrition, (2022), 76, 12, (1733-1739), 10.1038/s41430-022-01178-3)
European Journal of Clinical Nutrition
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Multicentre Delphi study of physicians resulted in quality indicators for young infants with fever without source in emergency departments
Acta Paediatrica, International Journal of Paediatrics, Vol. 112, Núm. 9, pp. 1962-1969
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Setting priorities for an agenda within the Spanish pediatric emergency medicine research network
European Journal of Pediatrics, Vol. 182, Núm. 8, pp. 3549-3558
2021
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Correction to: Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population (Orphanet Journal of Rare Diseases, (2021), 16, 1, (104), 10.1186/s13023-021-01729-0)
Orphanet Journal of Rare Diseases
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Febrile young infants with abnormal urine dipstick at low risk of invasive bacterial infection
Archives of Disease in Childhood, Vol. 106, Núm. 8, pp. 758-763
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Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population
Orphanet Journal of Rare Diseases, Vol. 16, Núm. 1
2020
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Clinical and Molecular Description of 16 Families With Heterozygous IHH Variants
The Journal of clinical endocrinology and metabolism, Vol. 105, Núm. 8
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Recommendations for Diagnosis and Treatment of Pseudohypoparathyroidism and Related Disorders: An Updated Practical Tool for Physicians and Patients
Hormone Research in Paediatrics, Vol. 93, Núm. 3, pp. 182-196
2019
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Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes
Orphanet Journal of Rare Diseases, Vol. 14, Núm. 1
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Implication in Paediatrics of the First International Consensus Statement for the Diagnosis and management of pseudohypoparathyroidism and related disorders
Anales de Pediatria, Vol. 90, Núm. 2, pp. 125.e1-125.e12
2018
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Brachydactyly type C due to a nonsense mutation in the GDF5 gene
Anales de Pediatria, Vol. 88, Núm. 2, pp. 107-109
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Diagnosis and management of pseudohypoparathyroidism and related disorders: First international Consensus Statement
Nature Reviews Endocrinology, Vol. 14, Núm. 8, pp. 476-500
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What to consider when pseudohypoparathyroidism is ruled out: IPPSD and differential diagnosis
BMC Medical Genetics, Vol. 19, Núm. 1
2017
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Aetiology and outcomes of potentially serious infections in febrile infants less than 3 months old
Anales de Pediatria, Vol. 87, Núm. 1, pp. 42-49
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International variability in gastrointestinal decontamination with acute poisonings
Pediatrics, Vol. 140, Núm. 2
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Prehospital management of acute childhood poisoning in Spain
Emergencias, Vol. 29, Núm. 3, pp. 178-181
2015
2014
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Diferencias territoriales en las intoxicaciones agudas en menores de 14 años en España
Anales de Pediatria, Vol. 82, Núm. 1, pp. e39-e43
2013
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Evolution of the quality of research in the Spanish society of pediatric emergency medicine (SEUP)
Emergencias
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Increasing incidence of pediatric inflammatory bowel disease in Spain (1996-2009): The SPIRIT registry
Inflammatory Bowel Diseases, Vol. 19, Núm. 1, pp. 73-80