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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'SNP
Claire 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 syndrome
Fanny 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 study
Anne-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 investigation
Alexandre 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 mutations
Astrid 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 haemochromatosis
Julien 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 Syndrome
Anne 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 Population
Bénédicte 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 Recurrence
Jessica 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 trial
Julien Hogan, Aubriana Perez, Anne-Laure Sellier-Leclerc, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 84) with videos related to
Sort By:
Page
of 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'SNP
Claire 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 syndrome
Fanny 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 study
Anne-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 investigation
Alexandre 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 mutations
Astrid 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 haemochromatosis
Julien 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 Syndrome
Anne 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 Population
Bénédicte 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 Recurrence
Jessica 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 trial
Julien Hogan, Aubriana Perez, Anne-Laure Sellier-Leclerc, et al.
Page
of 9