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Dominique Chauveau

Showing results (81-90 of 104) with videos related to

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Nephrologie & Therapeutique|February 21, 2024
Kidney biopsy for the diagnosis and treatment of kidney diseases. Recommendations from the French speaking Society of Nephrology (SFNDT) and French National Authority for Health (HAS) 2022Louis de Laforcade, Mickaël Bobot, Jean-Jacques Boffa, et al.
Journal of the American Society of Nephrology : JASN|October 22, 2003
A cluster of mutations in the UMOD gene causes familial juvenile hyperuricemic nephropathy with abnormal expression of uromodulinKarin Dahan, Olivier Devuyst, Michèle Smaers, et al.
Clinical Journal of the American Society of Nephrology : CJASN|March 17, 2012
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: phenotype-genotype correlation and outcome in 32 patients with CLDN16 or CLDN19 mutationsAstrid Godron, Jérôme Harambat, Valérie Boccio, et al.
European Journal of Internal Medicine|June 27, 2021
Systemic autoimmune disorders associated with thrombotic microangiopathy: A cross-sectional analysis from the French National TMA registry: Systemic autoimmune disease-associated TMANihal Martis, Matthieu Jamme, Corinne Bagnis-Isnard, et al.
Kidney International|January 11, 2017
The clinicopathologic characteristics of kidney diseases related to monotypic IgA depositsMarguerite Vignon, Camille Cohen, Stanislas Faguer, et al.
Transplantation|November 12, 2015
Calcineurin Inhibitors Downregulate HNF-1β and May Affect the Outcome of HNF1B Patients After Renal TransplantationStanislas Faguer, Laure Esposito, Audrey Casemayou, et al.
Diabetes|October 27, 2005
Large genomic rearrangements in the hepatocyte nuclear factor-1beta (TCF2) gene are the most frequent cause of maturity-onset diabetes of the young type 5Christine Bellanné-Chantelot, Séverine Clauin, Dominique Chauveau, et al.
Eclinicalmedicine|December 1, 2025
The personalized approach to rituximab treatment in membranous nephropathy: a multi-center randomized controlled trialVesna Brglez, Maxime Teisseyre, Kévin Zorzi, et al.
American Journal of Hematology|January 31, 2017
Thrombotic thrombocytopenic purpura misdiagnosed as autoimmune cytopenia: Causes of diagnostic errors and consequence on outcome. Experience of the French thrombotic microangiopathies reference centreMaximilien Grall, Elie Azoulay, Lionel Galicier, et al.
RMD Open|January 22, 2026
Impact of ANCA specificity on risk of cardiovascular events and death in ANCA-associated vasculitisJon Idoate Lacasia, Morgane Mourguet, Thomas Villeneuve, et al.
Pageof 11

Showing results (81-90 of 104) with videos related to

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Pageof 11
Nephrologie & Therapeutique|February 21, 2024
Kidney biopsy for the diagnosis and treatment of kidney diseases. Recommendations from the French speaking Society of Nephrology (SFNDT) and French National Authority for Health (HAS) 2022Louis de Laforcade, Mickaël Bobot, Jean-Jacques Boffa, et al.
Journal of the American Society of Nephrology : JASN|October 22, 2003
A cluster of mutations in the UMOD gene causes familial juvenile hyperuricemic nephropathy with abnormal expression of uromodulinKarin Dahan, Olivier Devuyst, Michèle Smaers, et al.
Clinical Journal of the American Society of Nephrology : CJASN|March 17, 2012
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: phenotype-genotype correlation and outcome in 32 patients with CLDN16 or CLDN19 mutationsAstrid Godron, Jérôme Harambat, Valérie Boccio, et al.
European Journal of Internal Medicine|June 27, 2021
Systemic autoimmune disorders associated with thrombotic microangiopathy: A cross-sectional analysis from the French National TMA registry: Systemic autoimmune disease-associated TMANihal Martis, Matthieu Jamme, Corinne Bagnis-Isnard, et al.
Kidney International|January 11, 2017
The clinicopathologic characteristics of kidney diseases related to monotypic IgA depositsMarguerite Vignon, Camille Cohen, Stanislas Faguer, et al.
Transplantation|November 12, 2015
Calcineurin Inhibitors Downregulate HNF-1β and May Affect the Outcome of HNF1B Patients After Renal TransplantationStanislas Faguer, Laure Esposito, Audrey Casemayou, et al.
Diabetes|October 27, 2005
Large genomic rearrangements in the hepatocyte nuclear factor-1beta (TCF2) gene are the most frequent cause of maturity-onset diabetes of the young type 5Christine Bellanné-Chantelot, Séverine Clauin, Dominique Chauveau, et al.
Eclinicalmedicine|December 1, 2025
The personalized approach to rituximab treatment in membranous nephropathy: a multi-center randomized controlled trialVesna Brglez, Maxime Teisseyre, Kévin Zorzi, et al.
American Journal of Hematology|January 31, 2017
Thrombotic thrombocytopenic purpura misdiagnosed as autoimmune cytopenia: Causes of diagnostic errors and consequence on outcome. Experience of the French thrombotic microangiopathies reference centreMaximilien Grall, Elie Azoulay, Lionel Galicier, et al.
RMD Open|January 22, 2026
Impact of ANCA specificity on risk of cardiovascular events and death in ANCA-associated vasculitisJon Idoate Lacasia, Morgane Mourguet, Thomas Villeneuve, et al.
Pageof 11