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Stéphane Decramer

Showing results (81-90 of 107) with videos related to

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Kidney International Reports|May 20, 2024
Steroid-Resistant Nephrotic Syndrome due to <i>NPHS2</i> Variants Is Not Associated With Posttransplant RecurrenceJessica Kachmar, Olivia Boyer, Beata Lipska-Ziętkiewicz, et al.
Rheumatology (Oxford, England)|April 27, 2026
Belimumab use in pediatric-onset systemic lupus erythematosus: a status report in France from a retrospective multicentre descriptive studyDorian Bigey-Frau, Damia Leguevaques, Heloise Reumaux, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 14, 2015
Clinical characteristics and outcomes of childhood-onset ANCA-associated vasculitis: a French nationwide studyAnne-Sylvia Sacri, Tristan Chambaraud, Bruno Ranchin, et al.
The Journal of Pathology|May 14, 2021
Mapping of the amniotic fluid proteome of fetuses with congenital anomalies of the kidney and urinary tract identifies plastin 3 as a protein involved in glomerular integrityCamille Fédou, Mylène Camus, Ophélie Lescat, et al.
Journal of the American Society of Nephrology : JASN|July 4, 2015
Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney DiseaseMarie-Pierre Audrézet, Christine Corbiere, Said Lebbah, et al.
Proteomics. Clinical Applications|February 5, 2010
CE-MS analysis of the human urinary proteome for biomarker discovery and disease diagnosticsJoshua J Coon, Petra Zürbig, Mohammed Dakna, et al.
British Journal of Clinical Pharmacology|May 24, 2025
Population pharmacokinetic modelling of prednisolone in systemic lupus erythematosus patients: Analysis of exposure and disease activityNaïm Bouazza, Michaela Semeraro, Gabrielle Lui, et al.
European Journal of Human Genetics : EJHG|September 5, 2019
School level of children carrying a HNF1B variant or a deletionFanny Laliève, Stéphane Decramer, Laurence Heidet, et al.
The Journal of Clinical Investigation|August 14, 2020
Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosisHélène Louis-Dit-Picard, Ilektra Kouranti, Chloé Rafael, et al.
Joint Bone Spine|January 1, 2017
Familial and syndromic lupus share the same phenotype as other early-onset forms of lupusOlivia Weill, Stéphane Decramer, Christophe Malcus, et al.
Pageof 11

Showing results (81-90 of 107) with videos related to

Sort By:
Pageof 11
Kidney International Reports|May 20, 2024
Steroid-Resistant Nephrotic Syndrome due to <i>NPHS2</i> Variants Is Not Associated With Posttransplant RecurrenceJessica Kachmar, Olivia Boyer, Beata Lipska-Ziętkiewicz, et al.
Rheumatology (Oxford, England)|April 27, 2026
Belimumab use in pediatric-onset systemic lupus erythematosus: a status report in France from a retrospective multicentre descriptive studyDorian Bigey-Frau, Damia Leguevaques, Heloise Reumaux, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 14, 2015
Clinical characteristics and outcomes of childhood-onset ANCA-associated vasculitis: a French nationwide studyAnne-Sylvia Sacri, Tristan Chambaraud, Bruno Ranchin, et al.
The Journal of Pathology|May 14, 2021
Mapping of the amniotic fluid proteome of fetuses with congenital anomalies of the kidney and urinary tract identifies plastin 3 as a protein involved in glomerular integrityCamille Fédou, Mylène Camus, Ophélie Lescat, et al.
Journal of the American Society of Nephrology : JASN|July 4, 2015
Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney DiseaseMarie-Pierre Audrézet, Christine Corbiere, Said Lebbah, et al.
Proteomics. Clinical Applications|February 5, 2010
CE-MS analysis of the human urinary proteome for biomarker discovery and disease diagnosticsJoshua J Coon, Petra Zürbig, Mohammed Dakna, et al.
British Journal of Clinical Pharmacology|May 24, 2025
Population pharmacokinetic modelling of prednisolone in systemic lupus erythematosus patients: Analysis of exposure and disease activityNaïm Bouazza, Michaela Semeraro, Gabrielle Lui, et al.
European Journal of Human Genetics : EJHG|September 5, 2019
School level of children carrying a HNF1B variant or a deletionFanny Laliève, Stéphane Decramer, Laurence Heidet, et al.
The Journal of Clinical Investigation|August 14, 2020
Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosisHélène Louis-Dit-Picard, Ilektra Kouranti, Chloé Rafael, et al.
Joint Bone Spine|January 1, 2017
Familial and syndromic lupus share the same phenotype as other early-onset forms of lupusOlivia Weill, Stéphane Decramer, Christophe Malcus, et al.
Pageof 11