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

2024

  1. Hypomagnesaemia with varying degrees of extrarenal symptoms as a consequence of heterozygous CNNM2 variants

    Scientific Reports, Vol. 14, Núm. 1

2021

  1. Impact of covid-19 on patients in radiotherapy oncology departaments in Spain

    Radiotherapy and Oncology

2020

  1. Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis

    Molecular Genetics and Genomic Medicine, Vol. 8, Núm. 11

2019

  1. Characterization of two novel mutations in the claudin-16 and claudin-19 genes that cause familial hypomagnesemia with hypercalciuria and nephrocalcinosis

    Gene, Vol. 689, pp. 227-234

2013

  1. Pediatric cyanide poisoning by fire smoke inhalation: A European expert consensus

    Pediatric Emergency Care, Vol. 29, Núm. 11, pp. 1234-1240

2007

  1. Molecular analysis of the CLCN5 gene in Dent's disease: First mutation identified in a patient from South America

    Clinical Nephrology, Vol. 68, Núm. 6, pp. 367-372

2004

  1. Changes in pediatric toxic dose of acetaminophen [8]

    American Journal of Emergency Medicine