Publicaciones en colaboración con investigadores/as de Universidad del País Vasco/Euskal Herriko Unibertsitatea (21)

2023

  1. Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3

    Scientific reports, Vol. 13, Núm. 1, pp. 12587

  2. Hypercalcemia in patients with mutations in NR3C2 and SCNN1B

    Medicina Clinica

2022

  1. Flexible multiplex PCR to detect SARS-CoV-2, coronavirus OC43 and influenza A virus in nasopharyngeal swab samples

    Journal of Applied Microbiology, Vol. 133, Núm. 6, pp. 3534-3545

  2. Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study

    Nephrology Dialysis Transplantation, Vol. 37, Núm. 12, pp. 2474-2486

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. Hereditary distal renal tubular acidosis: Genotypic correlation, evolution to long term, and new therapeutic perspectives

    Nefrologia, Vol. 41, Núm. 4, pp. 383-390

  3. Importance of timely treatment initiation in infantile-onset pompe disease, a single-centre experience

    Children, Vol. 8, Núm. 11

  4. Molecular aspects and long-term outcome of patients with primary distal renal tubular acidosis

    Pediatric Nephrology, Vol. 36, Núm. 10, pp. 3133-3142

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

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

2017

  1. Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome

    PLoS ONE, Vol. 12, Núm. 3

2015

  1. Novel mutations associated with nephrogenic diabetes insipidus. A clinical-genetic study

    European Journal of Pediatrics, Vol. 174, Núm. 10, pp. 1373-1385

2013

  1. Genetics of Type III Bartter Syndrome in Spain, Proposed Diagnostic Algorithm

    PLoS ONE, Vol. 8, Núm. 9

2011

  1. Hipomagnesemia renal hereditaria

    Revista Espanola de Pediatria, Vol. 67, Núm. 6, pp. 347-353

2010

  1. Dosis de aclaramiento en insuficiencia renal aguda

    Nefrologia, Vol. 30, Núm. 2, pp. 147-150

2003

  1. Análisis estadístico de la incidencia de cánceres «de novo» en pacientes trasplantados renales: Una nueva metodología de estudio

    Nefrologia, Vol. 23, Núm. 5, pp. 395-398

  2. Safety and efficacy of tacrolimus rescue therapy in 55 kidney transplant patients treated with cyclosporine

    Transplantation Proceedings

2001

  1. Assessment of integrated replacement therapy in patients with terminal renal insufficiency: selection vs election

    Nefrología : publicación oficial de la Sociedad Española Nefrologia, Vol. 21 Suppl 5, pp. 4-13

  2. Presentation of cancers in recipients of a solid-organ transplant

    Nefrología : publicación oficial de la Sociedad Española Nefrologia, Vol. 21, Núm. 6, pp. 528-537

1998

  1. Sindrome hemofagocitico en la infancia: A proposito de 4 casos

    Anales Espanoles de Pediatria, Vol. 49, Núm. 3, pp. 289-293

1997

  1. Aminoglycoside-associated Fanconi's syndrome: An underrecognized entity

    NEPHRON, Vol. 77, Núm. 2, pp. 205-211