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Kidney International|September 30, 2011
Nephrocalcinosis and urolithiasis in childrenSandra Habbig, Bodo Bernhard Beck, Bernd Hoppe
Pediatric Nephrology (Berlin, Germany)|April 30, 2017
Expanding the role of vasopressin antagonism in polycystic kidney diseases: From adults to children?Peter Janssens, Caroline Weydert, Stephanie De Rechter, et al.
Molecular and Cellular Pediatrics|February 24, 2021
Molecular causes of congenital anomalies of the kidney and urinary tract (CAKUT)Stefan Kohl, Sandra Habbig, Lutz T Weber, et al.
Expert Opinion on Investigational Drugs|November 22, 2012
Hyperoxaluria and systemic oxalosis: an update on current therapy and future directionsBodo B Beck, Heike Hoyer-Kuhn, Heike Göbel, et al.
Pediatric Nephrology (Berlin, Germany)|February 4, 2021
Complement activation in children with Streptococcus pneumoniae associated hemolytic uremic syndromeJohannes Holle, Sandra Habbig, Alexander Gratopp, et al.
Clinical Nephrology|May 16, 2017
A case report on the exceptional coincidence of two inherited renal disorders: ADPKD and Alport syndromeKathrin Ebner, Nadine Reintjes, Markus Feldkötter, et al.
Pediatric Nephrology (Berlin, Germany)|February 13, 2021
Differential assessment of fluid compartments by bioimpedance in pediatric patients with kidney diseasesSandra M Frey, Bruno Vogt, Giacomo D Simonetti, et al.
HGG Advances|April 2, 2025
Severe Joubert syndrome in family with homozygous POC1B p.Arg106Pro variant is due to a co-inherited deep-intronic mutation in the neighboring CEP290 geneChristian Betz, Björn Reusch, Thomas Langmann, et al.
Clinical Nephrology|October 30, 2018
Discontinuation of maintenance therapy in frequently relapsing nephrotic syndromeJulia Vogd, Agnes Hackl, Sandra Habbig, et al.
BMC Nephrology|April 17, 2015
Loss of Dgcr8-mediated microRNA expression in the kidney results in hydronephrosis and renal malformationMalte P Bartram, Claudia Dafinger, Sandra Habbig, et al.
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