Pediatría y sus áreas específicas

2023

1. A Network Meta-analysis of Dexamethasone for Preventing Postextubation Upper Airway Obstruction in Children

   Annals of the American Thoracic Society, Vol. 20, Núm. 1, pp. 118-130

2. Adaptation, reliability and validity of health-related quality of life questionnaires: Disabkids chronic and specific diabetes disease in children and adolescents with diabetes mellitus type 1

   Endocrinologia, Diabetes y Nutricion, Vol. 70, pp. 18-26

3. Adolescent cancer care: What has changed in Spain in the past decade?

   Anales de Pediatria, Vol. 98, Núm. 2, pp. 129-135

4. Alpha-1 antitrypsin deficiency and Pi*S and Pi*Z SERPINA1 variants are associated with asthma exacerbations

   Pulmonology

5. Altered Red Blood Cell Fatty Acid and Serum Adipokine Profiles in Subjects with Obesity

   Biomedicines, Vol. 11, Núm. 12

6. Autoimmune Diabetes From Childhood to Adulthood: The Role of Pancreatic Autoantibodies and HLA-DRB1 Genotype

   The Journal of clinical endocrinology and metabolism, Vol. 108, Núm. 11, pp. e1341-e1346

7. Autosomal dominant polycystic kidney disease in young adults

   Clinical Kidney Journal, Vol. 16, Núm. 6, pp. 985-995

8. 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

9. Coeliac Disease Case–Control Study: Has the Time Come to Explore beyond Patients at Risk?

   Nutrients, Vol. 15, Núm. 5

10. Diagnostic and therapeutic management of vesico-ureteral reflux in pediatric kidney transplantation—Results of an online survey on behalf of the European Society for Paediatric Nephrology

    Pediatric Transplantation, Vol. 27, Núm. 2

11. Dual latent tuberculosis screening with tuberculin skin tests and QuantiFERON-TB assays before TNF-α inhibitor initiation in children in Spain

    European Journal of Pediatrics, Vol. 182, Núm. 1, pp. 307-317

12. Germline heterozygous exons 8–11 pathogenic BARD1 gene deletion reported for the first time in a family with suspicion of a hereditary colorectal cancer syndrome: more than an incidental finding?

    Hereditary Cancer in Clinical Practice, Vol. 21, Núm. 1

13. Haploidentical vs. HLA-matched donor hematopoietic stem-cell transplantation for pediatric patients with acute lymphoblastic leukemia in second remission: A collaborative retrospective study of the Spanish Group for Bone Marrow Transplantation in Children (GETMON/GETH) and the Spanish Childhood Relapsed ALL Board (ReALLNet)

    Frontiers in Pediatrics, Vol. 11

14. Identification of germline cancer predisposition variants in pediatric sarcoma patients from somatic tumor testing

    Scientific Reports, Vol. 13, Núm. 1

15. Position statement on infection screening, prophylaxis, and vaccination in pediatric patients with rheumatic diseases and immunosuppressive therapies, part 2: infection prophylaxis

    European Journal of Pediatrics, Vol. 182, Núm. 9, pp. 4271-4284

16. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

    Genome Medicine, Vol. 15, Núm. 1

17. Rituximab-associated hypogammaglobulinemia in children with idiopathic nephrotic syndrome: results of an ESPN survey

    Pediatric Nephrology, Vol. 38, Núm. 9, pp. 3035-3042

18. The Value of the Second QuantiFERON-TB Gold-Plus Antigen Tube at Diagnosis and at Treatment Completion in Spanish Children With Tuberculosis

    Pediatric Infectious Disease Journal, Vol. 42, Núm. 11, pp. 1017-1020

19. Treatment and long-term outcome in primary nephrogenic diabetes insipidus

    Nephrology Dialysis Transplantation, Vol. 38, Núm. 10, pp. 2120-2130

20. Trombocitopenia inmune neonatal, una patología poco conocida y un reto diagnóstico

    Boletín de la Sociedad Vasco-Navarra de pediatría = Euskal Herriko Pediatria Elkartearen aldizkaria, Núm. 124, pp. 85-89