Publicaciones (96) Publicaciones en las que ha participado algún/a investigador/a

2021

  1. 2-Deoxy-D-glucose couples mitochondrial DNA replication with mitochondrial fitness and promotes the selection of wild-type over mutant mitochondrial DNA

    Nature Communications, Vol. 12, Núm. 1

  2. 3D Printable Conducting and Biocompatible PEDOT-graft-PLA Copolymers by Direct Ink Writing

    Macromolecular Rapid Communications, Vol. 42, Núm. 12

  3. A Novel Noninvasive Method Based on Salivary Inflammatory Biomarkers for the Screening of Celiac Disease

    Cellular and Molecular Gastroenterology and Hepatology

  4. A Validated WISC-V Short-Form to Estimate Intellectual Functioning in Very Preterm Children at Early School Age

    Frontiers in Psychology, Vol. 12

  5. A system pharmacology multi-omics approach toward uncontrolled pediatric asthma

    Journal of Personalized Medicine, Vol. 11, Núm. 6

  6. A systematic two-sample mendelian randomization analysis identifies shared genetic origin of endometriosis and associated phenotypes

    Life, Vol. 11, Núm. 1, pp. 1-12

  7. Accuracy of PECARN rule for predicting serious bacterial infection in infants with fever without a source

    Archives of Disease in Childhood, Vol. 106, Núm. 2, pp. 143-148

  8. Acidosis tubular renal distal hereditaria: correlación genotípica, evolución a largo plazo y nuevas perspectivas terapéuticas

    Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia, Vol. 41, Núm. 4, pp. 383-390

  9. Actions that should not be taken with a paediatric patient who has been exposed to a potentially toxic substance

    Anales de Pediatria, Vol. 94, Núm. 5, pp. 285-292

  10. Additive Prognostic Impact of Gastrointestinal Involvement in Severe Multisystem Langerhans Cell Histiocytosis

    Journal of Pediatrics, Vol. 237, pp. 65-70.e3

  11. Appropriateness of antidotes administered in spanish pediatric emergency departments

    Emergencias, Vol. 33, Núm. 6, pp. 479-481

  12. Blood enterovirus polymerase chain reaction testing in young febrile infants

    Archives of Disease in Childhood, Vol. 106, Núm. 12, pp. 1179-1183

  13. Bloqueo auriculoventricular congénito. Revisión temática

    Boletín de la Sociedad Vasco-Navarra de pediatría = Euskal Herriko Pediatria Elkartearen aldizkaria, Núm. 122, pp. 88-90

  14. COVID-19 aurkako txertoarekin erlazionatutako Guillain-Barré kasu baten aurkezpena

    Boletín de la Sociedad Vasco-Navarra de pediatría = Euskal Herriko Pediatria Elkartearen aldizkaria, Núm. 122, pp. 112-114

  15. Calidad de vida relacionada con la salud en pacientes pediátricos celíacos vascos

    Boletín de la Sociedad Vasco-Navarra de pediatría = Euskal Herriko Pediatria Elkartearen aldizkaria, Núm. 122, pp. 39-44

  16. Chemerin concentrations in infants born small for gestational age: correlations with triglycerides and parameters related to glucose homeostasis

    Journal of Physiology and Biochemistry, Vol. 77, Núm. 1, pp. 133-140

  17. Clinical value of NGS genomic studies for clinical management of pediatric and young adult bone sarcomas

    Cancers, Vol. 13, Núm. 21

  18. 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

  19. 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

  20. 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