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Pascal Houillier

Showing results (171-180 of 176) with videos related to

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Kidney International Reports|November 24, 2025
Clinical Characteristics, Symptoms, and Long-Term Outcomes in Gitelman SyndromeMichiel L A J Wieërs, Lise Allard, Viola D'Ambrosio, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 9, 2022
Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional studyMaartje F A Verploegen, Rosa Vargas-Poussou, Stephen B Walsh, et al.
Human Mutation|April 25, 2015
Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1Lamisse Mansour-Hendili, Anne Blanchard, Nelly Le Pottier, et al.
Nephron. Physiology|February 26, 2013
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsGraciana Jaureguiberry, Muriel De la Dure-Molla, David Parry, et al.
Geriatrie Et Psychologie Neuropsychiatrie Du Vieillissement|November 8, 2016
French law: what about a reasoned reimbursement of serum vitamin D assays?Jean-Claude Souberbielle, Claude Laurent Benhamou, Bernard Cortet, et al.
Annales De Biologie Clinique|August 15, 2014
[Weakening osteopathies, chronic kidney disease, malabsorption, biological anomalies of calium/phosphorus metabolism: appropriate indications for a reasoned reimbursment of serum vitamin D measurement]Jean-Claude Souberbielle, Claude Laurent Benhamou, Bernard Cortet, et al.
Pageof 18

Showing results (171-180 of 176) with videos related to

Sort By:
Pageof 18
You have reached the last page of results.This site can display upto 176 results.
Kidney International Reports|November 24, 2025
Clinical Characteristics, Symptoms, and Long-Term Outcomes in Gitelman SyndromeMichiel L A J Wieërs, Lise Allard, Viola D'Ambrosio, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 9, 2022
Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional studyMaartje F A Verploegen, Rosa Vargas-Poussou, Stephen B Walsh, et al.
Human Mutation|April 25, 2015
Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1Lamisse Mansour-Hendili, Anne Blanchard, Nelly Le Pottier, et al.
Nephron. Physiology|February 26, 2013
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsGraciana Jaureguiberry, Muriel De la Dure-Molla, David Parry, et al.
Geriatrie Et Psychologie Neuropsychiatrie Du Vieillissement|November 8, 2016
French law: what about a reasoned reimbursement of serum vitamin D assays?Jean-Claude Souberbielle, Claude Laurent Benhamou, Bernard Cortet, et al.
Annales De Biologie Clinique|August 15, 2014
[Weakening osteopathies, chronic kidney disease, malabsorption, biological anomalies of calium/phosphorus metabolism: appropriate indications for a reasoned reimbursment of serum vitamin D measurement]Jean-Claude Souberbielle, Claude Laurent Benhamou, Bernard Cortet, et al.
Pageof 18