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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 13, 2006
Novel OCRL1 mutations in patients with the phenotype of Dent diseaseBoris Utsch, Arend Bökenkamp, Marcus R Benz, et al.
Kidney International|September 10, 2015
Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidneyRik Westland, Miguel Verbitsky, Katarina Vukojevic, et al.
Kidney International Reports|December 12, 2022
Circulating Permeability Factors in Focal Segmental Glomerulosclerosis: <i>In</i> <i>V</i> <i>itro</i> DetectionSusan T Veissi, Bart Smeets, Joanna A E van Wijk, et al.
Annals of Clinical and Translational Neurology|March 17, 2026
A Depolarizing Leak in Sodium Bicarbonate Cotransporter NBCe1 Causes Brain EdemaQuinty Bisseling, Mark D Parker, Sven Kerst, et al.
Platelets|June 12, 2020
Harmonizing light transmission aggregometry in the Netherlands by implementation of the SSC-ISTH guidelineI C A Munnix, R Van Oerle, P Verhezen, et al.
Pediatric Nephrology (Berlin, Germany)|September 3, 2021
Long-term follow-up including extensive complement analysis of a pediatric C3 glomerulopathy cohortMarloes A H M Michels, Kioa L Wijnsma, Roel A J Kurvers, et al.
Pediatric Nephrology (Berlin, Germany)|October 9, 2016
Serological and genetic complement alterations in infection-induced and complement-mediated hemolytic uremic syndromeDineke Westra, Elena B Volokhina, Renate G van der Molen, 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.
Kidney International Reports|January 16, 2023
Early Eculizumab Withdrawal in Patients With Atypical Hemolytic Uremic Syndrome in Native Kidneys Is Safe and Cost-Effective: Results of the CUREiHUS StudyRomy N Bouwmeester, Caroline Duineveld, Kioa L Wijnsma, et al.
American Journal of Human Genetics|November 4, 2017
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney MalformationsSimone Sanna-Cherchi, Kamal Khan, Rik Westland, et al.
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