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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 26, 2024
Lung structural and functional impairments in young children with cystic fibrosis diagnosed following newborn screening - A nationwide observational studyBettina S Frauchiger, Corin Willers, Jasna Cotting, et al.
Kidney International Reports|May 7, 2026
German Clinical Practice Guideline on Microhematuria in Children and Young Adults: Evaluating Early Detection of Kidney DiseaseKay Latta, Jan Boeckhaus, Ina Weinreich, et al.
Pediatric Nephrology (Berlin, Germany)|January 26, 2025
Factors associated with statural growth in pediatric kidney transplant recipients with focus on metabolic acidosisAgnieszka Prytuła, Dries Reynders, Els Goetghebeur, et al.
Pediatric Nephrology (Berlin, Germany)|June 8, 2024
Morphological changes and their associations with clinical parameters in children with nephropathic cystinosis and chronic kidney disease prior to kidney replacement therapy over 25 yearsMalina Brügelmann, Sophia Müller, Alina V Bohlen, et al.
Pediatric Transplantation|June 11, 2022
Timing of reconstruction of the lower urinary tract in pediatric kidney transplant recipients: A CERTAIN multicenter analysis of current practiceChristian Patry, Britta Höcker, Luca Dello Strologo, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|June 7, 2012
An outbreak of Shiga toxin-producing Escherichia coli O104:H4 hemolytic uremic syndrome in Germany: presentation and short-term outcome in childrenSebastian Loos, Thurid Ahlenstiel, Brigitta Kranz, et al.
Open Forum Infectious Diseases|August 8, 2026
Pediatric Hemolytic Uremic Syndrome in North-Eastern Germany During the STEC O45:H2 Outbreak in 2025: Clinical Features and Short-Term OutcomesLea M Merz, Katja Doerry, Florian Buerger, et al.
Acta Neuropathologica|December 21, 2013
Disturbed function of the blood-cerebrospinal fluid barrier aggravates neuro-inflammationGijs Kooij, Kathrin Kopplin, Rosel Blasig, 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.
Pediatric Nephrology (Berlin, Germany)|January 23, 2019
HNF1B nephropathy has a slow-progressive phenotype in childhood-with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood RegistryChristine Okorn, Anne Goertz, Udo Vester, et al.
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