Publicaciones en colaboración con investigadores/as de Complejo Asistencial Universitario de León (12)

2023

  1. A second update on mapping the human genetic architecture of COVID-19

    Nature

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

2019

  1. NFKBIZ and CW6 in Adalimumab Response Among Psoriasis Patients: Genetic Association and Alternative Transcript Analysis

    Molecular Diagnosis and Therapy, Vol. 23, Núm. 5, pp. 627-633

  2. Risk of cardiovascular involvement in pediatric patients with X-linked hypophosphatemia

    Pediatric Nephrology, Vol. 34, Núm. 6, pp. 1077-1086

2018

  1. Marker of vitamin D status in healthy children: Free or total 25-hydroxyvitamin D?

    PLoS ONE, Vol. 13, Núm. 8

  2. Salt-losing tubulopathy and chronic dermatitis

    Kidney International, Vol. 94, Núm. 2, pp. 433

2008

  1. Urinary interleukin-6 is useful in distinguishing between upper and lower urinary tract infections

    Pediatric Nephrology, Vol. 23, Núm. 3, pp. 429-433

2007

  1. Strontium oral load test in children with idiopathic hypercalciuria

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

2001

  1. Alteraciones moleculares en los carcinomas epidermoides de la orofaringe

    Acta Otorrinolaringologica Espanola, Vol. 52, Núm. 1, pp. 24-31

  2. Asociación entre la integración del virus del papiloma humano y la pérdida de heterozigosidad del gen P53 en los carcinomas epidermoides de cabeza y cuello

    Acta Otorrinolaringologica Espanola, Vol. 52, Núm. 7, pp. 546-552

1995

  1. Effect of a low sodium diet on urinary elimination of cystine in cystinuric children

    Nephron, Vol. 71, Núm. 4, pp. 416-418