Pediatría y sus áreas específicas

2020

1. Availability, accessibility and delivery to patients of the 28 orphan medicines approved by the European Medicine Agency for hereditary metabolic diseases in the MetabERN network

   Orphanet Journal of Rare Diseases, Vol. 15, Núm. 1

2. Canavan gaixotasuna (aspartoazilasaren gabezia): Euskal Herriko lehen kasuaren eta Europako mutazio berri baten aurkezpena

   Osagaiz: osasun-zientzien aldizkaria, Vol. 4, Núm. 2, pp. 71-78

3. Changes from COVID-19. A perspective from internal pediatric medicine

   Anales de Pediatria, Vol. 93, Núm. 5, pp. 343.e1-343.e8

4. Consensus Document on Community-Acquired Pneumonia in Children. SENP-SEPAR-SEIP

   Archivos de Bronconeumologia, Vol. 56, Núm. 11, pp. 725-741

5. Diagnosis and treatment of acute tonsillopharyngitis. Consensus document update

   Anales de Pediatria, Vol. 93, Núm. 3, pp. 206.e1-206.e8

6. 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

7. Forty-One Individuals With Mutations in the AVP-NPII Gene Associated With Familial Neurohypophyseal Diabetes Insipidus

   The Journal of clinical endocrinology and metabolism, Vol. 105, Núm. 4

8. Gene signatures of early response to anti-TNF drugs in pediatric inflammatory bowel disease

   International Journal of Molecular Sciences, Vol. 21, Núm. 9

9. Genetic Predictors of Long-term Response to Antitumor Necrosis Factor Agents in Pediatric Inflammatory Bowel Disease

   Journal of pediatric gastroenterology and nutrition, Vol. 71, Núm. 4, pp. 508-515

10. Hemangiomatosis neonatal difusa. Presentación de un caso clínico

    Boletín de la Sociedad Vasco-Navarra de pediatría = Euskal Herriko Pediatria Elkartearen aldizkaria, Núm. 121, pp. 102-104

11. Hiperfosfatasemia transitoria benigna de la infancia, presentación de dos casos

    Boletín de la Sociedad Vasco-Navarra de pediatría = Euskal Herriko Pediatria Elkartearen aldizkaria, Núm. 121, pp. 105-108

12. Hypophosphataemic Rickets: Similar Phenotype of Different Diseases

    Advances in Therapy, Vol. 37, pp. 80-88

13. Ictus en la edad pediátrica y vacunación reciente de meningococo B. ¿Hay una relación causal?

    Boletín de la Sociedad Vasco-Navarra de pediatría = Euskal Herriko Pediatria Elkartearen aldizkaria, Núm. 121, pp. 111-112

14. Inequalities in diagnosis and registration of pediatric very rare tumors: a European study on pleuropulmonary blastoma

    European Journal of Pediatrics, Vol. 179, Núm. 5, pp. 749-756

15. Measurable Residual Disease Assessed by Flow-Cytometry Is a Stable Prognostic Factor for Pediatric T-Cell Acute Lymphoblastic Leukemia in Consecutive SEHOP Protocols Whereas the Impact of Oncogenetics Depends on Treatment

    Frontiers in Pediatrics, Vol. 8

16. Metabolismo fosfocálcico

    Pediatria Integral, Vol. 24, Núm. 5, pp. 268-275

17. Oocytes of women who are obese or overweight have lower levels of n-3 polyunsaturated fatty acids compared with oocytes of women with normal weight

    Fertility and Sterility, Vol. 113, Núm. 1, pp. 53-61

18. Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies

    Journal of Medical Genetics, Vol. 57, Núm. 4, pp. 258-268

19. Spanish Pediatric Inflammatory Bowel Disease Diagnostic Delay Registry: SPIDER Study From Sociedad Española de Gastroenterología, Hepatología y Nutrición Pediátrica

    Frontiers in Pediatrics, Vol. 8

20. Study protocol for a phase II, multicentre, prospective, non-randomised clinical trial to assess the safety and efficacy of infusing allogeneic activated and expanded natural killer cells as consolidation therapy for paediatric acute myeloblastic leukaemia

    BMJ Open, Vol. 10, Núm. 1