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Marguerite Hureaux

Showing results (1-10 of 35) with videos related to

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Molecular and Cellular Endocrinology|December 2, 2022
Genetic basis of nephrogenic diabetes insipidusMarguerite Hureaux, Rosa Vargas-Poussou
Medecine Sciences : M/S|March 21, 2023
[Major advances in pediatric nephro-genetics]Marguerite Hureaux, Laurence Heidet, Rosa Vargas-Poussou, et al.
Annals of the New York Academy of Sciences|January 9, 2023
Mechanisms of paracellular transport of magnesium in intestinal and renal epitheliaPascal Houillier, Loïc Lievre, Marguerite Hureaux, et al.
Clinical Kidney Journal|August 13, 2025
A puzzling renal Fanconi syndromeLudwig Haydock, Marguerite Hureaux, Maxime Hoffmann, et al.
Kidney International Reports|October 8, 2021
The variety of genetic defects explains the phenotypic heterogeneity of Familial Hyperkalemic HypertensionMarguerite Hureaux, Stephani Mazurkiewicz, Valerie Boccio, et al.
Journal of Nephrology|September 11, 2024
Prevalence of kidney failure in adults diagnosed with hereditary tubulopathiesMaureen Betton, Anne Blanchard, Pascal Houillier, et al.
The Journal of Steroid Biochemistry and Molecular Biology|October 5, 2020
Renin-aldosterone system evaluation over four decades in an extended family with autosomal dominant pseudohypoaldosteronism due to a deletion in the NR3C2 geneAaron Hanukoglu, Rosa Vargas-Poussou, Zohar Landau, et al.
Human Mutation|February 18, 2021
Diversity of functional alterations of the ClC-5 exchanger in the region of the proton glutamate in patients with Dent disease 1Imène Sakhi, Yohan Bignon, Nadia Frachon, et al.
Children (Basel, Switzerland)|November 10, 2020
A Rare Cause of Chronic Hypokalemia with Metabolic Alkalosis: Case Report and Differential DiagnosisCristina Bertulli, Marguerite Hureaux, Chiara De Mutiis, et al.
Molecular Cytogenetics|May 6, 2021
When a maternal heterozygous mutation of the CYP24A1 gene leads to infantile hypercalcemia through a maternal uniparental disomy of chromosome 20Marguerite Hureaux, Sandra Chantot-Bastaraud, Kévin Cassinari, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Molecular and Cellular Endocrinology|December 2, 2022
Genetic basis of nephrogenic diabetes insipidusMarguerite Hureaux, Rosa Vargas-Poussou
Medecine Sciences : M/S|March 21, 2023
[Major advances in pediatric nephro-genetics]Marguerite Hureaux, Laurence Heidet, Rosa Vargas-Poussou, et al.
Annals of the New York Academy of Sciences|January 9, 2023
Mechanisms of paracellular transport of magnesium in intestinal and renal epitheliaPascal Houillier, Loïc Lievre, Marguerite Hureaux, et al.
Clinical Kidney Journal|August 13, 2025
A puzzling renal Fanconi syndromeLudwig Haydock, Marguerite Hureaux, Maxime Hoffmann, et al.
Kidney International Reports|October 8, 2021
The variety of genetic defects explains the phenotypic heterogeneity of Familial Hyperkalemic HypertensionMarguerite Hureaux, Stephani Mazurkiewicz, Valerie Boccio, et al.
Journal of Nephrology|September 11, 2024
Prevalence of kidney failure in adults diagnosed with hereditary tubulopathiesMaureen Betton, Anne Blanchard, Pascal Houillier, et al.
The Journal of Steroid Biochemistry and Molecular Biology|October 5, 2020
Renin-aldosterone system evaluation over four decades in an extended family with autosomal dominant pseudohypoaldosteronism due to a deletion in the NR3C2 geneAaron Hanukoglu, Rosa Vargas-Poussou, Zohar Landau, et al.
Human Mutation|February 18, 2021
Diversity of functional alterations of the ClC-5 exchanger in the region of the proton glutamate in patients with Dent disease 1Imène Sakhi, Yohan Bignon, Nadia Frachon, et al.
Children (Basel, Switzerland)|November 10, 2020
A Rare Cause of Chronic Hypokalemia with Metabolic Alkalosis: Case Report and Differential DiagnosisCristina Bertulli, Marguerite Hureaux, Chiara De Mutiis, et al.
Molecular Cytogenetics|May 6, 2021
When a maternal heterozygous mutation of the CYP24A1 gene leads to infantile hypercalcemia through a maternal uniparental disomy of chromosome 20Marguerite Hureaux, Sandra Chantot-Bastaraud, Kévin Cassinari, et al.
Pageof 4