Pediatría
Departamento
Hospital Universitario Virgen del Rocío
Sevilla, EspañaPublicaciones en colaboración con investigadoras/es de Hospital Universitario Virgen del Rocío (63)
2024
2023
-
Characteristics and outcomes of the Spanish registry for pediatric patients with bicuspid aortic valve (REVAB)
Revista Espanola de Cardiologia, Vol. 76, Núm. 12, pp. 961-969
-
Loss of the matrix metalloproteinase-10 causes premature features of aging in satellite cells
Frontiers in Cell and Developmental Biology, Vol. 11
2022
-
Clinical spectrum of COVID-19 and risk factors associated with severity in Spanish children
European journal of pediatrics, Vol. 181, Núm. 3, pp. 1105-1115
-
Correction to: Position statement of the Spanish society of pediatric rheumatology on infection screening, prophylaxis, and vaccination of pediatric patients with rheumatic diseases and immunosuppressive therapies: part 1 (screening) (European Journal of Pediatrics, (2022), 181, 6, (2343-2354), 10.1007/s00431-022-04418-7)
European Journal of Pediatrics
-
Correlation of Anti-Tissue Transglutaminase Antibodies With the Mucosal Changes and IgA Status of Children With Celiac Disease
Journal of pediatric gastroenterology and nutrition, Vol. 75, Núm. 6, pp. 743-748
-
Current status of precision medicine in pediatric oncology in Spain: a consensus report by the Spanish Society of Paediatric Haematology and Oncology (SEHOP)
Clinical and Translational Oncology, Vol. 24, Núm. 5, pp. 809-815
-
Langerhans cell histiocytosis. Advances in pathogenesis and clinical practice
Anales de Pediatria, Vol. 97, Núm. 2, pp. 130.e1-130.e7
-
Multicentre study of magnet ingestion in Spanish paediatric emergency departments
Anales de Pediatria, Vol. 97, Núm. 5, pp. 310-316
-
Neuroblastoma in Spain: Linking the national clinical database and epidemiological registries – A study by the Joint Action on Rare Cancers
Cancer Epidemiology, Vol. 78
2021
-
Collaborative model for diagnosis and treatment of very rare diseases: experience in Spain with thymidine kinase 2 deficiency
Orphanet Journal of Rare Diseases, Vol. 16, Núm. 1
-
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
-
Cystathionine ß-synthase deficiency in the E-HOD registry-part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis
Journal of Inherited Metabolic Disease, Vol. 44, Núm. 3, pp. 677-692
-
Diagnostic Accuracy of the Panbio Severe Acute Respiratory Syndrome Coronavirus 2 Antigen Rapid Test Compared with Reverse-Transcriptase Polymerase Chain Reaction Testing of Nasopharyngeal Samples in the Pediatric Population
Journal of Pediatrics, Vol. 232, pp. 287-289.e4
-
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
-
Interferon-Gamma Release Assays Differentiate between Mycobacterium avium Complex and Tuberculous Lymphadenitis in Children
Journal of Pediatrics, Vol. 236, pp. 211-218.e2
-
Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population
Orphanet Journal of Rare Diseases, Vol. 16, Núm. 1
2020
-
A multicenter national survey of children with SARS-CoV-2 infection admitted to Spanish Pediatric Intensive Care Units
Intensive Care Medicine
-
Distinct molecular profile of IRF4-rearranged large B-cell lymphoma
Blood, Vol. 135, Núm. 4, pp. 274-286
-
Evaluation of the impact of the Spanish consensus document on the approach to osteoarticular infections in Spain through the Paediatrics Osteoarticular Infections Network (RIOPED)
Anales de Pediatria, Vol. 93, Núm. 5, pp. 289-296