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Scientific Reports|September 30, 2020
Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD)Kathrin Burgmaier, Gema Ariceta, Martin Bald, et al.
Kidney International Reports|January 16, 2023
Hyperparathyroidism Is an Independent Risk Factor for Allograft Dysfunction in Pediatric Kidney TransplantationAgnieszka Prytula, Rukshana Shroff, Kai Krupka, et al.
Clinical Journal of the American Society of Nephrology : CJASN|March 31, 2015
Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1Anja Lehnhardt, Claartje Karnatz, Thurid Ahlenstiel-Grunow, et al.
Orphanet Journal of Rare Diseases|June 3, 2021
The European Rare Kidney Disease Registry (ERKReg): objectives, design and initial resultsGiulia Bassanese, Tanja Wlodkowski, Aude Servais, et al.
Nature Reviews. Nephrology|June 15, 2026
Clinical practice recommendations for the diagnosis and management of nephropathic cystinosisKatharina Hohenfellner, Elke Wühl, Dieter Haffner, et al.
Human Mutation|November 8, 2006
Schimke immunoosseous dysplasia: suggestions of genetic diversityJ Marietta Clewing, Helen Fryssira, David Goodman, et al.
The Journal of Clinical Investigation|October 16, 2019
Human C-terminal CUBN variants associate with chronic proteinuria and normal renal functionMathilda Bedin, Olivia Boyer, Aude Servais, et al.
Nature Genetics|June 25, 2013
ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3Sylvia Hoff, Jan Halbritter, Daniel Epting, et al.
Transplantation|June 17, 2026
Evidence- and Consensus-based European Guideline for Immunosuppressive Therapy After Pediatric Kidney TransplantationAnna Grünewald, Thurid Ahlenstiel-Grunow, Zainab Arslan, et al.
The Journal of Pediatrics|May 14, 2018
Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney DiseaseKathrin Burgmaier, Kevin Kunzmann, Gema Ariceta, et al.
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