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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 23, 2016
Genetic risk variants for membranous nephropathy: extension of and association with other chronic kidney disease aetiologiesPeggy Sekula, Yong Li, Horia C Stanescu, et al.
Pediatric Nephrology (Berlin, Germany)|January 10, 2022
Whole-exome sequencing and variant spectrum in children with suspected inherited renal tubular disorder: the East India Tubulopathy Gene StudyRajiv Sinha, Subal Pradhan, Sushmita Banerjee, et al.
Pediatric Nephrology (Berlin, Germany)|October 5, 2021
Long-term kidney function in children with Wilms tumour and constitutional WT1 pathogenic variantMaria Pia Falcone, Kathryn Pritchard-Jones, Jesper Brok, et al.
Kidney International|December 23, 2016
Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies ConferenceAnne Blanchard, Detlef Bockenhauer, Davide Bolignano, 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.
Pediatric Nephrology (Berlin, Germany)|February 1, 2025
Characteristics of patients with autosomal polycystic kidney disease reaching kidney failure by age 40Stijn Wigerinck, Pieter Schellekens, Byron H Smith, et al.
The Journal of Clinical Investigation|August 27, 2024
Quantifying variant contributions in cystic kidney disease using national-scale whole-genome sequencingOmid Sadeghi-Alavijeh, Melanie My Chan, Gabriel T Doctor, et al.
Kidney & Blood Pressure Research|May 25, 2025
CFHR5 Nephropathy Case Report: A Novel Variant Characterized by Tubulointerstitial Kidney DiseaseRita Santarsiere, Giulia Florio, Annalisa Gonnella, et al.
Nature Reviews. Nephrology|October 22, 2024
International expert consensus statement on the diagnosis and management of congenital nephrogenic diabetes insipidus (arginine vasopressin resistance)Elena Levtchenko, Gema Ariceta, Olga Arguedas Flores, et al.
The Journal of Physiology|February 9, 2011
Altered electroretinograms in patients with KCNJ10 mutations and EAST syndromeDorothy A Thompson, Sally Feather, Horia C Stanescu, et al.
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