Friedhelm Hildebrandt
7PUBLICATIONS
3CO-AUTHORS
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Publications (7)
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|Jan 23, 2026
Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndrome.Bshara Mansour, Katharina Lemberg, Ronen Schneider
|Nov 11, 2021
Whole exome sequencing identifies monogenic forms of nephritis in a previously unsolved cohort of children with steroid-resistant nephrotic syndrome and hematuria.Hongbo Xiao, Friedhelm Hildebrandt
|Sep 07, 2021
Prevalence and clinical prediction of mitochondrial disorders in a large neuropediatric cohort.Amelie T van der Ven, Jessika Johannsen, Fanny Kortüm
|Jun 24, 2019
COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans.Thomas M Kitzler, Ronen Schneider, Stefan Kohl
|Feb 20, 2019
Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis.Ali Amar, Amar J Majmundar, Ihsan Ullah
|Sep 19, 2017
Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center.Weizhen Tan, Svjetlana Lovric, Shazia Ashraf
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