Rosa Poussou-Vargas

Paris, France

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 83 publications

SLC4A1 mutations that cause distal renal tubular acidosis alter cytoplasmic pH and cellular autophagy.

SLC4A1 mutations that cause distal renal tubular acidosis alter cytoplasmic pH and cellular autophagy.

Journal: eLife

Published: March 04, 2026

Clinical Characteristics, Symptoms, and Long-Term Outcomes in Gitelman Syndrome.

Clinical Characteristics, Symptoms, and Long-Term Outcomes in Gitelman Syndrome.

Journal: Kidney international reports

Published: July 31, 2025

A puzzling renal Fanconi syndrome.

A puzzling renal Fanconi syndrome.

Journal: Clinical kidney journal

Published: October 14, 2024

International expert consensus statement on the diagnosis and management of congenital nephrogenic diabetes insipidus (arginine vasopressin resistance).

International expert consensus statement on the diagnosis and management of congenital nephrogenic diabetes insipidus (arginine vasopressin resistance).

Journal: Nature reviews. Nephrology

Published: September 13, 2024

CCDC158: A novel regulator in renal proximal tubular endocytosis unveiled through exome sequencing and interactome analysis.

CCDC158: A novel regulator in renal proximal tubular endocytosis unveiled through exome sequencing and interactome analysis.

Journal: Journal of cellular physiology

Published: February 15, 2024

The SLC6A18 Transporter Is Most Likely a Na-Dependent Glycine/Urea Antiporter Responsible for Urea Secretion in the Proximal Straight Tubule: Influence of This Urea Secretion on Glomerular Filtration Rate.

The SLC6A18 Transporter Is Most Likely a Na-Dependent Glycine/Urea Antiporter Responsible for Urea Secretion in the Proximal Straight Tubule: Influence of This Urea Secretion on Glomerular Filtration Rate.

Journal: Nephron

Published: February 13, 2024

Prevalence of kidney failure in adults diagnosed with hereditary tubulopathies.

Prevalence of kidney failure in adults diagnosed with hereditary tubulopathies.

Journal: Journal of nephrology

Published: February 06, 2024

X-linked transient antenatal Bartter syndrome related to MAGED2 gene: Enriching the phenotypic description and pathophysiologic investigation.

X-linked transient antenatal Bartter syndrome related to MAGED2 gene: Enriching the phenotypic description and pathophysiologic investigation.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: November 30, 2023

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

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

Journal: Scientific reports

Published: August 03, 2023

Clinical Findings and Genetic Analysis of Nine Mexican Families with Bartter Syndrome.

Clinical Findings and Genetic Analysis of Nine Mexican Families with Bartter Syndrome.

Journal: Archives of medical research

Published: April 04, 2023

Major advances in pediatric nephro-genetics

Major advances in pediatric nephro-genetics

Journal: Medecine sciences : M/S

Published: March 21, 2023

Comment to "Recommendation on an updated standardization of serum magnesium reference ranges".

Comment to "Recommendation on an updated standardization of serum magnesium reference ranges".

Journal: European journal of nutrition

Published: June 26, 2022

Showing 1-12 of 83

Last Updated: 09/26/2026