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Orphanet Journal of Rare Diseases|March 10, 2022
Primary URECs: a source to better understand the pathology of renal tubular epithelia in pediatric hereditary cystic kidney diseasesWolfgang H Ziegler, Sarah Lüdiger, Fatima Hassan, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 20, 2025
Polycystic Kidney Disease in Children: The Current Status and the Next HorizonMelissa A Cadnapaphornchai, Katherine M Dell, Charlotte Gimpel, et al.
The Journal of Biological Chemistry|March 2, 2011
Nephrocystin-4 regulates Pyk2-induced tyrosine phosphorylation of nephrocystin-1 to control targeting to monociliaMax C Liebau, Katja Höpker, Roman U Müller, et al.
The Journal of Clinical Investigation|May 5, 2010
PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndromeInga Ebermann, Jennifer B Phillips, Max C Liebau, et al.
Radiology|January 2, 2019
Imaging of Kidney Cysts and Cystic Kidney Diseases in Children: An International Working Group Consensus StatementCharlotte Gimpel, E Fred Avni, Luc Breysem, et al.
Pediatric Nephrology (Berlin, Germany)|February 4, 2025
Urinary Dickkopf-related protein 3 as a novel biomarker for kidney function decline in children with Alport syndromeJan Boeckhaus, Burkhard Tönshoff, Lutz T Weber, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|March 23, 2017
Intermediate Follow-up of Pediatric Patients With Hemolytic Uremic Syndrome During the 2011 Outbreak Caused by E. coli O104:H4Sebastian Loos, Wiebke Aulbert, Bernd Hoppe, et al.
Scientific Reports|May 30, 2019
Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD)Kathrin Burgmaier, Samuel Kilian, Bert Bammens, et al.
Experimental & Molecular Medicine|July 1, 2018
Targeted deletion of the AAA-ATPase Ruvbl1 in mice disrupts ciliary integrity and causes renal disease and hydrocephalusClaudia Dafinger, Markus M Rinschen, Lori Borgal, et al.
Nature Reviews. Nephrology|May 24, 2019
International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young peopleCharlotte Gimpel, Carsten Bergmann, Detlef Bockenhauer, et al.
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