For: | Almalki AH, Sadagah LF, Qureshi M, Maghrabi H, Algain A, Alsaeed A. Atypical hemolytic-uremic syndrome due to complement factor I mutation. World J Nephrol 2017; 6(6): 243-250 [PMID: 29226095 DOI: 10.5527/wjn.v6.i6.243] |
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URL: | https://www.wjgnet.com/2220-6124/full/v6/i6/243.htm |
Number | Citing Articles |
1 |
Farhana Begum, Nida Khan, Stephanie Boisclair, Deepa A. Malieckal, David Chitty. Complement Inhibitors in the Management of Complement-Mediated Hemolytic Uremic Syndrome and Paroxysmal Nocturnal Hemoglobinuria. American Journal of Therapeutics 2023; 30(3): e209 doi: 10.1097/MJT.0000000000001609
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2 |
Omar K Abughanimeh, Muhamed Baljevic, Alex Nester. Novel Heterozygous Missense Variants in Diacylglycerol Kinase Epsilon and Complement Factor I: Potential Pathogenic Association With Atypical Hemolytic Uremic Syndrome. Cureus 2024; doi: 10.7759/cureus.52633
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3 |
Daigo Nakazawa. Targeting complement in kidney transplantation: Therapeutic approaches based on preclinical and experimental evidence. Transplantation Reviews 2025; 39(1): 100887 doi: 10.1016/j.trre.2024.100887
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4 |
Yulia V. Lavrishcheva, Alexander A. Yakovenko, Dmitrii A. Kudlai. The experience of using the Russian biosimilar of the original drug eculizumab for the treatment of patients with atypical hemolytic-uremic syndrome. Terapevticheskii arkhiv 2020; 92(6): 76 doi: 10.26442/00403660.2020.06.000649
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