Publicaciones en las que colabora con Laura Espinosa Román (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. Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population

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

2013

  1. Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

    PLoS ONE, Vol. 8, Núm. 1

2011

  1. Gitelman syndrome in Gypsy paediatric patients carrying the same intron 9 + 1 G>T mutation. Clinical features and impact on quality of life

    Nephrology Dialysis Transplantation, Vol. 26, Núm. 1, pp. 151-155

2007

  1. A missense mutation in the chloride/proton ClC-5 antiporter gene results in increased expression of an alternative mRNA form that lacks exons 10 and 11. Identification of seven new CLCN5 mutations in patients with Dent's disease

    Journal of Human Genetics, Vol. 52, Núm. 3, pp. 255-261

2003

  1. Renin-angiotensin system polymorphisms and renal scarring

    Pediatric Nephrology, Vol. 18, Núm. 2, pp. 110-114

2000

  1. Analysis of chromosome 6p in Spanish families with recessive polycystic kidney disease

    Pediatric Nephrology, Vol. 14, Núm. 3, pp. 205-207