Publicaciones en colaboración con investigadores/as de Hospital Severo Ochoa (7)

2021

  1. 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

  2. Familial hypercholesterolaemia in twin brothers born using in-vitro fertilisation with donor semen and ovules

    Anales de Pediatria, Vol. 94, Núm. 3, pp. 179-180

  3. Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population

    Orphanet Journal of Rare Diseases, Vol. 16, Núm. 1

2017

  1. A new SLC12A3 founder mutation (p.Val647Met) in Gitelman's syndrome patients of Roma ancestry

    Nefrologia, Vol. 37, Núm. 4, pp. 423-428

2007

  1. Strontium oral load test in children with idiopathic hypercalciuria

    Pediatric Nephrology, Vol. 22, Núm. 9, pp. 1303-1307

2003

  1. IL-1α (-889) promoter polymorphism is a risk factor for osteomyelitis

    American Journal of Medical Genetics, Vol. 119 A, Núm. 2, pp. 132-136

1996

  1. Expression of collagenase-3 in the rat ovary during the ovulatory process

    Journal of Endocrinology, Vol. 149, Núm. 3, pp. 405-415