Renaud De La Faille

Place Amélie Raba Léon
Bordeaux, 33000, France

Last Updated: 09/26/2026

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Found 10 publications

Epidemiology of urinary stone composition in the Southwest of France: A 23-year single-center retrospective study.

Epidemiology of urinary stone composition in the Southwest of France: A 23-year single-center retrospective study.

Journal: The French journal of urology

Published: May 12, 2025

Performance of real-time PCR in suspected haemodialysis catheter-related bloodstream infection: a proof-of-concept study.

Performance of real-time PCR in suspected haemodialysis catheter-related bloodstream infection: a proof-of-concept study.

Journal: Clinical kidney journal

Published: July 03, 2022

Impact of menopausal status on kidney adaptation after unilateral nephrectomy for kidney donation in women.

Impact of menopausal status on kidney adaptation after unilateral nephrectomy for kidney donation in women.

Journal: Journal of nephrology

Published: February 01, 2021

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

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

Journal: Journal of the American Society of Nephrology : JASN

Published: January 14, 2019

A prospective comparison of dynamic contrast-enhanced MRI and 51Cr-EDTA clearance for glomerular filtration rate measurement in 42 kidney transplant recipients.

A prospective comparison of dynamic contrast-enhanced MRI and 51Cr-EDTA clearance for glomerular filtration rate measurement in 42 kidney transplant recipients.

Journal: European journal of radiology

Published: November 20, 2018

Late diagnosis of primary hyperoxaluria type III.

Late diagnosis of primary hyperoxaluria type III.

Journal: Annals of clinical biochemistry

Published: October 16, 2016

Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations.

Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations.

Journal: Journal of medical genetics

Published: May 11, 2016

Hypomagnesemia as First Clinical Manifestation of ADTKD-HNF1B: A Case Series and Literature Review.

Hypomagnesemia as First Clinical Manifestation of ADTKD-HNF1B: A Case Series and Literature Review.

Journal: American journal of nephrology

Published: September 05, 2015

Observations of a large Dent disease cohort.

Observations of a large Dent disease cohort.

Journal: Kidney international

Published: July 22, 2015

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

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

Journal: Human mutation

Published: February 11, 2015

Showing 1-10 of 10

Last Updated: 09/26/2026