Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Vincent Guigonis

Showing results (71-80 of 84) with videos related to

Pageof 9
Sort By:
Pediatric Nephrology (Berlin, Germany)|March 3, 2025
A "Trial within a Cohort" platform for pediatric clinical trials on idiopathic nephrotic syndrome: scope, objectives, and design of the retrospective-prospective cohort PIN'SNPClaire Bahans, Olivia Boyer, Olivier Dunand, et al.
Archives of Disease in Childhood|October 18, 2014
Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndromeFanny Laffargue, Sylvie Bourthoumieu, Brigitte Llanas, et al.
Pediatric Nephrology (Berlin, Germany)|May 8, 2023
Outcome of children with IgA vasculitis with nephritis treated with steroids: a matched controlled studyAnne-Lise Mary, Stéphanie Clave, Caroline Rousset-Rouviere, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2024
X-linked transient antenatal Bartter syndrome related to MAGED2 gene: Enriching the phenotypic description and pathophysiologic investigationAlexandre Buffet, Mathilde Filser, Alexandra Bruel, 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.
Journal of Pediatric Gastroenterology and Nutrition|August 1, 2014
Transient neonatal liver disease after maternal antenatal intravenous Ig infusions in gestational alloimmune liver disease associated with neonatal haemochromatosisJulien Baruteau, Sophie Heissat, Pierre Broué, et al.
Clinical Journal of the American Society of Nephrology : CJASN|November 18, 2017
Prevalence of Novel <i>MAGED2</i> Mutations in Antenatal Bartter SyndromeAnne Legrand, Cyrielle Treard, Isabelle Roncelin, et al.
Kidney International Reports|May 2, 2022
Social Deprivation Is Associated With Lower Access to Pre-emptive Kidney Transplantation and More Urgent-Start Dialysis in the Pediatric PopulationBénédicte Driollet, Florian Bayer, Theresa Kwon, et al.
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.
BMJ Open|September 24, 2020
Efficacy and safety of intravenous immunoglobulin with rituximab versus rituximab alone in childhood-onset steroid-dependent and frequently relapsing nephrotic syndrome: protocol for a multicentre randomised controlled trialJulien Hogan, Aubriana Perez, Anne-Laure Sellier-Leclerc, et al.
Pageof 9

Showing results (71-80 of 84) with videos related to

Sort By:
Pageof 9
Pediatric Nephrology (Berlin, Germany)|March 3, 2025
A "Trial within a Cohort" platform for pediatric clinical trials on idiopathic nephrotic syndrome: scope, objectives, and design of the retrospective-prospective cohort PIN'SNPClaire Bahans, Olivia Boyer, Olivier Dunand, et al.
Archives of Disease in Childhood|October 18, 2014
Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndromeFanny Laffargue, Sylvie Bourthoumieu, Brigitte Llanas, et al.
Pediatric Nephrology (Berlin, Germany)|May 8, 2023
Outcome of children with IgA vasculitis with nephritis treated with steroids: a matched controlled studyAnne-Lise Mary, Stéphanie Clave, Caroline Rousset-Rouviere, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2024
X-linked transient antenatal Bartter syndrome related to MAGED2 gene: Enriching the phenotypic description and pathophysiologic investigationAlexandre Buffet, Mathilde Filser, Alexandra Bruel, 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.
Journal of Pediatric Gastroenterology and Nutrition|August 1, 2014
Transient neonatal liver disease after maternal antenatal intravenous Ig infusions in gestational alloimmune liver disease associated with neonatal haemochromatosisJulien Baruteau, Sophie Heissat, Pierre Broué, et al.
Clinical Journal of the American Society of Nephrology : CJASN|November 18, 2017
Prevalence of Novel <i>MAGED2</i> Mutations in Antenatal Bartter SyndromeAnne Legrand, Cyrielle Treard, Isabelle Roncelin, et al.
Kidney International Reports|May 2, 2022
Social Deprivation Is Associated With Lower Access to Pre-emptive Kidney Transplantation and More Urgent-Start Dialysis in the Pediatric PopulationBénédicte Driollet, Florian Bayer, Theresa Kwon, et al.
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.
BMJ Open|September 24, 2020
Efficacy and safety of intravenous immunoglobulin with rituximab versus rituximab alone in childhood-onset steroid-dependent and frequently relapsing nephrotic syndrome: protocol for a multicentre randomised controlled trialJulien Hogan, Aubriana Perez, Anne-Laure Sellier-Leclerc, et al.
Pageof 9