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[Electrolyte disorders].
Satanovskij RM, Renders L. Satanovskij RM, et al. Among authors: renders l. MMW Fortschr Med. 2015 Jul 23;157(13):54-9; quiz 60. doi: 10.1007/s15006-015-2728-8. MMW Fortschr Med. 2015. PMID: 26206040 Review. German. No abstract available.
A new missense mutation in UMOD gene leads to severely reduced serum uromodulin concentrations - A tool for the diagnosis of uromodulin-associated kidney disease.
Satanovskij R, Bader A, Block M, Herbst V, Schlumberger W, Haack T, Nockher WA, Heemann U, Renders L, Schmaderer C, Angermann S, Wen M, Meitinger T, Scherberich J, Steubl D. Satanovskij R, et al. Among authors: renders l. Clin Biochem. 2017 Feb;50(3):155-158. doi: 10.1016/j.clinbiochem.2016.10.003. Epub 2016 Oct 10. Clin Biochem. 2017. PMID: 27729211
Heterozygous COL4A3 Variants in Histologically Diagnosed Focal Segmental Glomerulosclerosis.
Braunisch MC, Büttner-Herold M, Günthner R, Satanovskij R, Riedhammer KM, Herr PM, Klein HG, Wahl D, Küchle C, Renders L, Heemann U, Schmaderer C, Hoefele J. Braunisch MC, et al. Among authors: renders l. Front Pediatr. 2018 Jun 12;6:171. doi: 10.3389/fped.2018.00171. eCollection 2018. Front Pediatr. 2018. PMID: 29946535 Free PMC article.
[The hepatorenal syndrome].
Heemann U, Füeßl HS, Renders L. Heemann U, et al. Among authors: renders l. Dtsch Med Wochenschr. 2015 Oct;140(20):1520-3. doi: 10.1055/s-0041-105807. Epub 2015 Oct 7. Dtsch Med Wochenschr. 2015. PMID: 26445256 German.
122 results