Adolescence-onset atypical hemolytic uremic syndrome: is it different from infant-onset?-Reference-Cited by-同舟云学术

Adolescence-onset atypical hemolytic uremic syndrome: is it different from infant-onset?

Published:2024-05-05 Issue: Volume: Page:
ISSN:1342-1751
Container-title:Clinical and Experimental Nephrology
language:en
Short-container-title:Clin Exp Nephrol

Author:

Celegen Kubra,Gulhan Bora,Fidan Kibriya,Yuksel Selcuk,Yilmaz Neslihan,Yılmaz Aysun Caltik,Demircioğlu Kılıç Beltinge,Gokce Ibrahim,Kavaz Tufan Aslı,Kalyoncu Mukaddes,Nalcacıoglu Hulya,Ozlu Sare Gulfem,Kurt Sukur Eda Didem,Canpolat Nur,K. Bayazit Aysun,Çomak Elif,Tabel Yılmaz,Tulpar Sebahat,Celakil Mehtap,Bek Kenan,Zeybek Cengiz,Duzova Ali,Özçakar Zeynep Birsin,Topaloglu Rezan,Soylemezoglu Oguz,Ozaltin Fatih

Funder

Scientific Research Projects Coordination Unit of Hacettepe University

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s10157-024-02505-7.pdf

Reference36 articles.

1. Fremeaux-Bacchi V, Fakhouri F, Garnier A, Bienaime F, Dragon-Durey MA, Ngo S, et al. Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults. Clin J Am Soc Nephrol. 2013;8(4):554–62. https://doi.org/10.2215/CJN.04760512.

2. Noris M, Caprioli J, Bresin E, Mossali C, Pianetti G, Gamba S, et al. Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype. Clin J Am Soc Nephrol. 2010;5(10):1844–59. https://doi.org/10.2215/CJN.02210310.

3. Schaefer F, Ardissino G, Ariceta G, Fakhouri F, Scully M, Isbel N, et al. Clinical and genetic predictors of atypical hemolytic uremic syndrome phenotype and outcome. Kidney Int. 2018;94(2):408–18. https://doi.org/10.1016/j.kint.2018.02.029.

4. Feitz WJC, van de Kar N, Orth-Höller D, van den Heuvel L, Licht C. The genetics of atypical hemolytic uremic syndrome. Med Genet Mitteil Berufsver Med Genet. 2018;30(4):400–9. https://doi.org/10.1007/s11825-018-0216-0.

5. Ozaltin F, Li B, Rauhauser A, An SW, Soylemezoglu O, Gonul II, et al. DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN. J Am Soc Nephrol JASN. 2013;24(3):377–84. https://doi.org/10.1681/asn.2012090903.

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1. Correction to: Adolescence‑onset atypical hemolytic uremic syndrome: is it different from infant‑onset?;Clinical and Experimental Nephrology;2024-07-06