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List of works by Rosa Vargas-Poussou

A Rare Cause of Chronic Hypokalemia with Metabolic Alkalosis: Case Report and Differential Diagnosis

scientific article published on 05 November 2020

A mouse model for distal renal tubular acidosis reveals a previously unrecognized role of the V-ATPase a4 subunit in the proximal tubule

scientific article

A pseudo-dominant form of Gitelman's syndrome

scientific article published on 22 August 2011

Clinical Characteristics of Familial Hypocalciuric Hypercalcaemia Type 1: A Multicentre Study of 77 Adult Patients

scientific article published on 29 April 2020

Clinical utility gene card for: Familial hypomagnesemia with hypercalciuria and nephrocalcinosis with/without severe ocular involvement

scientific article published on 3 September 2014

Effect of hydrochlorothiazide on urinary calcium excretion in dent disease: an uncontrolled trial

scientific article

Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelman's syndrome

scientific article

Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences

scientific article published on 10 March 2016

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: phenotype-genotype correlation and outcome in 32 patients with CLDN16 or CLDN19 mutations

scientific article published on 15 March 2012

Fetal urine biochemistry in antenatal Bartter syndrome: a case report

scientific article published on 08 August 2016

Genetic testing in the diagnosis of chronic kidney disease: recommendations for clinical practice

scientific article published on 11 July 2021

Indomethacin, amiloride, or eplerenone for treating hypokalemia in Gitelman syndrome

scientific article

Investigation of Vestibular Function in Adult Patients with Gitelman Syndrome: Results of an Observational Study

scientific article published on 23 November 2020

Localization of tubular adaptation to renal sodium loss in Gitelman syndrome

scientific article published on 12 January 2012

Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1.

scientific article published on 11 June 2015

Mutations in ATP6V1B1 and ATP6V0A4 genes cause recessive distal renal tubular acidosis in Mexican families

scientific article published on 14 February 2016

Novel CLCN5 mutations in patients with Dent's disease result in altered ion currents or impaired exchanger processing

scientific article

Observations of a large Dent disease cohort

scientific article published on 22 June 2016

Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome

scientific article

Renal, Ocular, and Neuromuscular Involvements in Patients with CLDN19 Mutations ⬇️

scientific article published on October 28, 2010

Resistance to Insulin in Patients with Gitelman Syndrome and a Subtle Intermediate Phenotype in Heterozygous Carriers: A Cross-Sectional Study

scientific article published on 08 July 2019

Spectrum of mutations in Gitelman syndrome

scientific article

p.Ala541Thr variant of MEN1 gene: a non deleterious polymorphism or a pathogenic mutation?

scientific article

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