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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 14, 2015
Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemiaJeroen H F de Baaij, Eiske M Dorresteijn, Eric A M Hennekam, et al.
Frontiers in Immunology|November 13, 2023
Modeling complement activation on human glomerular microvascular endothelial cellsKes H Stevens, Laura M Baas, Thea J A M van der Velden, et al.
Frontiers in Immunology|August 30, 2021
Different Aspects of Classical Pathway Overactivation in Patients With C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative GlomerulonephritisMarloes A H M Michels, Nicole C A J van de Kar, Sanne A W van Kraaij, 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.
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.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 2, 2012
Best supportive care and therapeutic plasma exchange with or without eculizumab in Shiga-toxin-producing E. coli O104:H4 induced haemolytic-uraemic syndrome: an analysis of the German STEC-HUS registryJan T Kielstein, Gernot Beutel, Susanne Fleig, et al.
Kidney International|August 20, 2023
Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney diseaseLaura R Claus, Chuan Chen, Jennifer Stallworth, et al.
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