Publicaciones en colaboración con investigadores/as de Universitat de Barcelona (8)

2021

  1. BMP8 and activated brown adipose tissue in human newborns

    Nature Communications, Vol. 12, Núm. 1

2020

  1. Holistic approach of the care of the infant with hypoxic-ischaemic encephalopathy in Spain

    Anales de Pediatria, Vol. 92, Núm. 5, pp. 286-296

2018

  1. Care of the newborn with perinatal asphyxia candidate for therapeutic hypothermia during the first six hours of life in Spain

    Anales de Pediatria, Vol. 89, Núm. 4, pp. 211-221

  2. Protocolo de homocistinuria

    Protocolos de diagnóstico y tratamiento de los errores congénitos del metabolismo (Ergon), pp. 167-180

2016

  1. Vertically transmitted cytomegalovirus infection in newborn preterm infants

    Journal of Perinatal Medicine, Vol. 44, Núm. 5, pp. 485-490

2007

  1. Erratum: The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America (Journal of Human Genetics 51, (305-313) DOI: 10.1007/s10038-006-0362-0)

    Journal of Human Genetics

2006

  1. The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America

    Journal of Human Genetics, Vol. 51, Núm. 4, pp. 305-313

2003

  1. Spectrum of CBS mutations in 16 homocystinuric patients from the Iberian Peninsula: high prevalence of T191M and absence of I278T or G307S.

    Human mutation, Vol. 22, Núm. 1, pp. 103