Publications (133) Publications in which a researcher has participated

2020

  1. A clinical scoring system for congenital contractural arachnodactyly

    Genetics in Medicine, Vol. 22, Núm. 1, pp. 124-131

  2. A new clinical score to identify children at low risk for appendicitis

    American Journal of Emergency Medicine, Vol. 38, Núm. 3, pp. 554-561

  3. A positive nitrite test was an independent risk factor for invasive bacterial infections in infants under 90 days of age with fever without source

    Acta Paediatrica, International Journal of Paediatrics, Vol. 109, Núm. 11, pp. 2316-2323

  4. Acidosis tubular renal distal (tipo 1) en un lactante

    Boletín de la Sociedad Vasco-Navarra de pediatría = Euskal Herriko Pediatria Elkartearen aldizkaria, Núm. 121, pp. 130-131

  5. Actualización del documento de consenso sobre el diagnóstico y tratamiento de la faringoamigdalitis aguda

    Anales de Pediatría: Publicación Oficial de la Asociación Española de Pediatría ( AEP ), Vol. 93, Núm. 3, pp. 206-206

  6. Acute severe paediatric asthma: Study protocol for the development of a core outcome set, a Pediatric Emergency Reserarch Networks (PERN) study

    Trials, Vol. 21, Núm. 1

  7. Addition of terlipressin to initial volume resuscitation in a pediatric model of hemorrhagic shock improves hemodynamics and cerebral perfusion

    PLoS ONE, Vol. 15, Núm. 7

  8. Adin erlatiboaren efektua eskola-garaian

    Uztaro: giza eta gizarte-zientzien aldizkaria, Núm. 113, pp. 93-109

  9. Associations of paediatric demyelinating and encephalitic syndromes with myelin oligodendrocyte glycoprotein antibodies: a multicentre observational study

    The Lancet Neurology, Vol. 19, Núm. 3, pp. 234-246

  10. Autoantibodies against type I IFNs in patients with life-threatening COVID-19

    Science, Vol. 370, Núm. 6515

  11. 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

  12. Basal renal function in paediatric patients: correlation of methods that depend on a 24 h urine collection with simpler methods that do not require a timed urine

    Anales de Pediatria, Vol. 92, Núm. 2, pp. 65-70

  13. Bebé colodión e ictiosis. A propósito de un caso

    Boletín de la Sociedad Vasco-Navarra de pediatría = Euskal Herriko Pediatria Elkartearen aldizkaria, Núm. 121, pp. 82-84

  14. Brain circuit alterations and cognitive disability in late-onset cobalamin d disorder

    Journal of Clinical Medicine, Vol. 9, Núm. 4

  15. Cambios a partir de la COVID-19: una perspectiva desde la pediatría interna hospitalaria

    Anales de Pediatría: Publicación Oficial de la Asociación Española de Pediatría ( AEP ), Vol. 93, Núm. 5, pp. 343-343

  16. 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

  17. Cervical pregnancy in assisted reproduction: an analysis of risk factors in 91,067 ongoing pregnancies

    Reproductive BioMedicine Online, Vol. 40, Núm. 3, pp. 355-361

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

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

  19. Clinical prediction rule for distinguishing bacterial from aseptic meningitis

    Pediatrics, Vol. 146, Núm. 3

  20. Complex I deficiency, due to NDUFAF4 mutations, causes severe mitochondrial dysfunction and is associated to early death and dysmorphia

    Mitochondrion, Vol. 55, pp. 78-84