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Hypertension (Dallas, Tex. : 1979)|April 8, 2025
Hypertension Management Dynamics in Pediatric CKD: Insights From the 4C StudyAnke Doyon, Aysun Karabay Bayazit, Ali Duzova, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 26, 2020
Active vitamin D is cardioprotective in experimental uraemia but not in children with CKD Stages 3-5Anne Schön, Maren Leifheit-Nestler, Jennifer Deppe, et al.
Kidney International Reports|June 9, 2025
Longitudinal Lipid Trajectories and Progression of CKD in ChildrenUwe Querfeld, Marietta Kirchner, Francesca Mencarelli, et al.
Pediatric Nephrology (Berlin, Germany)|May 8, 2024
Dyslipidemia in children with chronic kidney disease-findings from the Cardiovascular Comorbidity in Children with Chronic Kidney Disease (4C) studyFrancesca Mencarelli, Karolis Azukaitis, Marietta Kirchner, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 1, 2015
Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression ConsortiumMatthias Wuttke, Craig S Wong, Elke Wühl, et al.
Clinical Journal of the American Society of Nephrology : CJASN|November 10, 2016
Cardiovascular Phenotypes in Children with CKD: The 4C StudyFranz Schaefer, Anke Doyon, Karolis Azukaitis, et al.
American Journal of Human Genetics|March 15, 2011
CNNM2, encoding a basolateral protein required for renal Mg2+ handling, is mutated in dominant hypomagnesemiaMarchel Stuiver, Sergio Lainez, Constanze Will, et al.
Eclinicalmedicine|July 25, 2024
Changes in the cardiovascular risk profile in children approaching kidney replacement therapyPriyanka Khandelwal, Jonas Hofstetter, Karolis Azukaitis, et al.
Nature Communications|October 14, 2014
Germline variants in the SEMA4A gene predispose to familial colorectal cancer type XEduard Schulz, Petra Klampfl, Stefanie Holzapfel, et al.
Human Mutation|July 1, 2015
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney DiseaseJulia Vodopiutz, Rainer Seidl, Daniela Prayer, et al.
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