Mireia Aguirre
Barakaldo, PV, Spain
Last Updated: 09/26/2026
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Found 8 publications
Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3.
Journal: Scientific reports
Published: January 13, 2023
On the relevance of thrombomodulin variants in atypical hemolytic uremic syndrome.
Journal: Kidney international
Published: December 02, 2022
Molecular aspects and long-term outcome of patients with primary distal renal tubular acidosis.
Journal: Pediatric nephrology (Berlin, Germany)
Published: November 06, 2020
Characterization of two novel mutations in the claudin-16 and claudin-19 genes that cause familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Journal: Gene
Published: October 10, 2018
Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome.
Journal: PloS one
Published: July 15, 2016
Novel mutations associated with nephrogenic diabetes insipidus. A clinical-genetic study.
Journal: European journal of pediatrics
Published: January 13, 2015
Genetics of type III Bartter syndrome in Spain, proposed diagnostic algorithm.
Journal: PloS one
Published: May 08, 2013
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Last Updated: 09/26/2026