Ulrike Walden
Augsburg, BY, Germany
Last Updated: 09/26/2026
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Found 8 publications
Terminal 4q duplication and extended 10q deletion in a preterm infant with linear growth restriction: transcriptomic evidence of disrupted developmental and metabolic pathways.
Journal: Frontiers in pediatrics
Published: April 08, 2026
SGLT2-Inhibition in Patients With Alport Syndrome.
Journal: Kidney international reports
Published: July 23, 2024
The need for tumor surveillance of children and adolescents with cancer predisposition syndromes: a retrospective cohort study in a tertiary-care children's hospital.
Journal: European journal of pediatrics
Published: July 26, 2021
HNF1B nephropathy has a slow-progressive phenotype in childhood-with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry.
Journal: Pediatric nephrology (Berlin, Germany)
Published: May 14, 2018
Presentation of pediatric Henoch-Schönlein purpura nephritis changes with age and renal histology depends on biopsy timing.
Journal: Pediatric nephrology (Berlin, Germany)
Published: June 18, 2017
Phenotypic Spectrum of Children with Nephronophthisis and Related Ciliopathies.
Journal: Clinical journal of the American Society of Nephrology : CJASN
Published: February 03, 2017
Novel biomarker and easy to perform ELISA for monitoring complement inhibition in patients with atypical hemolytic uremic syndrome treated with eculizumab.
Journal: Journal of immunological methods
Published: August 07, 2015
Mutations in WDR19 encoding the intraflagellar transport component IFT144 cause a broad spectrum of ciliopathies.
Journal: Pediatric nephrology (Berlin, Germany)
Published: November 20, 2013
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Last Updated: 09/26/2026