Publicacións en colaboración con investigadores/as de Universidad de Cantabria (10)

2023

  1. Breastfeeding and Inborn Errors of Amino Acid and Protein Metabolism: A Spreadsheet to Calculate Optimal Intake of Human Milk and Disease-Specific Formulas

    Nutrients, Vol. 15, Núm. 16

2022

  1. A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy

    Communications Biology, Vol. 5, Núm. 1

2020

  1. Cribado selectivo de la hipofosfatasia en la población pediátrica del País Vasco

    Boletín de la Sociedad Vasco-Navarra de pediatría = Euskal Herriko Pediatria Elkartearen aldizkaria, Núm. 121, pp. 14-17

2017

  1. Utilidad de un dispositivo luminoso simple para mejorar el aprendizaje del masaje cardiaco

    Revista Espanola de Anestesiologia y Reanimacion, Vol. 64, Núm. 9, pp. 506-512

2009

  1. When rare diseases become urgent: Inborn errors of metabolism in primary care

    Atencion Primaria, Vol. 41, Núm. 4, pp. 223-228

  2. When rare diseases become urgent: inborn errors of metabolism in primary care

    Atencion primaria / Sociedad Española de Medicina de Familia y Comunitaria, Vol. 41, Núm. 4, pp. 221-226

2004

  1. Implications of upper respiratory tract infections and drugs in the clinical spectrum of Henoch-Schönlein purpura in children

    Clinical and Experimental Rheumatology, Vol. 22, Núm. 6, pp. 781-784

2002

  1. A new prognostic scoring system for meningococcal septic shock in children. Comparison with three other scoring systems

    Intensive Care Medicine, Vol. 28, Núm. 3, pp. 341-351

  2. Henoch-Schönlein purpura in children and adults: Clinical differences in a defined population

    Seminars in Arthritis and Rheumatism, Vol. 32, Núm. 3, pp. 149-156

2001

  1. Henoch-Schönlein purpura in children from northwestern Spain: A 20-year epidemiologic and clinical study

    Medicine, Vol. 80, Núm. 5, pp. 279-290