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Aurelia Bertholet-Thomas

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The New England Journal of Medicine|April 4, 2014
Nephropathic cystinosis--a gap between developing and developed nationsAurelia Bertholet-Thomas, Justine Bacchetta, Velibor Tasic, et al.
Pediatric Nephrology (Berlin, Germany)|March 19, 2025
Granulomatous nephropathy: have you thought about genetics?Enzo Vedrine, Lucie Bessenay, Carole Philipponnet, et al.
European Journal of Pediatrics|September 11, 2025
Descriptive cohort study of transient isolated tubular acidosis in early childhood: experience from a rare kidney disease expert centerHajer Charfi, Aurelia Bertholet-Thomas, Justine Bacchetta, et al.
Pediatric Transplantation|May 11, 2020
Eplet incompatibility in pediatric renal transplantationAndreea Liana Rãchişan, Valerie Dubois, Bruno Ranchin, et al.
Pediatric Nephrology (Berlin, Germany)|August 1, 2024
Unveiling atypical diagnoses: when whole-genome analysis performed for refractory infantile hypomagnesemia reveals primary hyperoxaluriaDima Kayal, Enzo Vedrine, Claire Goursaud, et al.
Pediatric Nephrology (Berlin, Germany)|March 22, 2024
Addressing the psychosocial aspects of transition to adult care in patients with cystinosisStella Stabouli, Anna Sommer, Stefanie Kraft, et al.
Kidney International|January 29, 2021
Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular DisordersMartin Konrad, Tom Nijenhuis, Gema Ariceta, et al.
Molecular Genetics & Genomic Medicine|July 19, 2017
Clinical and molecular characterization of cystinuria in a French cohort: relevance of assessing large-scale rearrangements and splicing variantsPascaline Gaildrat, Said Lebbah, Abdellah Tebani, et al.
Kidney International|September 12, 2020
Cystinuria: clinical practice recommendationAude Servais, Kay Thomas, Luca Dello Strologo, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 28, 2022
Clinical and genetic characteristics of Dent's disease type 1 in EuropeCarla Burballa, Gerard Cantero-Recasens, Larisa Prikhodina, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
The New England Journal of Medicine|April 4, 2014
Nephropathic cystinosis--a gap between developing and developed nationsAurelia Bertholet-Thomas, Justine Bacchetta, Velibor Tasic, et al.
Pediatric Nephrology (Berlin, Germany)|March 19, 2025
Granulomatous nephropathy: have you thought about genetics?Enzo Vedrine, Lucie Bessenay, Carole Philipponnet, et al.
European Journal of Pediatrics|September 11, 2025
Descriptive cohort study of transient isolated tubular acidosis in early childhood: experience from a rare kidney disease expert centerHajer Charfi, Aurelia Bertholet-Thomas, Justine Bacchetta, et al.
Pediatric Transplantation|May 11, 2020
Eplet incompatibility in pediatric renal transplantationAndreea Liana Rãchişan, Valerie Dubois, Bruno Ranchin, et al.
Pediatric Nephrology (Berlin, Germany)|August 1, 2024
Unveiling atypical diagnoses: when whole-genome analysis performed for refractory infantile hypomagnesemia reveals primary hyperoxaluriaDima Kayal, Enzo Vedrine, Claire Goursaud, et al.
Pediatric Nephrology (Berlin, Germany)|March 22, 2024
Addressing the psychosocial aspects of transition to adult care in patients with cystinosisStella Stabouli, Anna Sommer, Stefanie Kraft, et al.
Kidney International|January 29, 2021
Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular DisordersMartin Konrad, Tom Nijenhuis, Gema Ariceta, et al.
Molecular Genetics & Genomic Medicine|July 19, 2017
Clinical and molecular characterization of cystinuria in a French cohort: relevance of assessing large-scale rearrangements and splicing variantsPascaline Gaildrat, Said Lebbah, Abdellah Tebani, et al.
Kidney International|September 12, 2020
Cystinuria: clinical practice recommendationAude Servais, Kay Thomas, Luca Dello Strologo, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 28, 2022
Clinical and genetic characteristics of Dent's disease type 1 in EuropeCarla Burballa, Gerard Cantero-Recasens, Larisa Prikhodina, et al.
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