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Quoted phrase not found in phrase index: "CFH-Related Disorders"
Page 1
Mesangial C3 Deposition, Complement-Associated Variant, and Disease Progression in IgA Nephropathy.
Kang Y, Xu B, Shi S, Zhou X, Chen P, Liu L, Li Y, Leng Y, Lv J, Zhu L, Zhang H. Kang Y, et al. Clin J Am Soc Nephrol. 2023 Dec 1;18(12):1583-1591. doi: 10.2215/CJN.0000000000000290. Epub 2023 Aug 31. Clin J Am Soc Nephrol. 2023. PMID: 37651123
Our previous genome-wide association study identified complement factor H ( CFH ) variant rs6677604, tightly linked with the deletion of CFH -related protein 3 and CFH -related protein 1 genes ( deltaCFHR3-1 ), as IgA nephropathy susceptible variant, a …
Our previous genome-wide association study identified complement factor H ( CFH ) variant rs6677604, tightly linked with the deletion of …
Genetic prediction of ICU hospitalization and mortality in COVID-19 patients using artificial neural networks.
Asteris PG, Gavriilaki E, Touloumenidou T, Koravou EE, Koutra M, Papayanni PG, Pouleres A, Karali V, Lemonis ME, Mamou A, Skentou AD, Papalexandri A, Varelas C, Chatzopoulou F, Chatzidimitriou M, Chatzidimitriou D, Veleni A, Rapti E, Kioumis I, Kaimakamis E, Bitzani M, Boumpas D, Tsantes A, Sotiropoulos D, Papadopoulou A, Kalantzis IG, Vallianatou LA, Armaghani DJ, Cavaleri L, Gandomi AH, Hajihassani M, Hasanipanah M, Koopialipoor M, Lourenço PB, Samui P, Zhou J, Sakellari I, Valsami S, Politou M, Kokoris S, Anagnostopoulos A. Asteris PG, et al. J Cell Mol Med. 2022 Mar;26(5):1445-1455. doi: 10.1111/jcmm.17098. Epub 2022 Jan 22. J Cell Mol Med. 2022. PMID: 35064759 Free PMC article.
There is an unmet need of models for early prediction of morbidity and mortality of Coronavirus disease-19 (COVID-19). ...Through targeted next-generation sequencing, we identified variants in complement factor H/CFH, CFB, CFH-related, CFD, CD55, C3, C …
There is an unmet need of models for early prediction of morbidity and mortality of Coronavirus disease-19 (COVID-19). ...Thro …
Analysis of genetic and predisposing factors in Japanese patients with atypical hemolytic uremic syndrome.
Fan X, Yoshida Y, Honda S, Matsumoto M, Sawada Y, Hattori M, Hisanaga S, Hiwa R, Nakamura F, Tomomori M, Miyagawa S, Fujimaru R, Yamada H, Sawai T, Ikeda Y, Iwata N, Uemura O, Matsukuma E, Aizawa Y, Harada H, Wada H, Ishikawa E, Ashida A, Nangaku M, Miyata T, Fujimura Y. Fan X, et al. Mol Immunol. 2013 Jun;54(2):238-46. doi: 10.1016/j.molimm.2012.12.006. Epub 2013 Jan 8. Mol Immunol. 2013. PMID: 23314101
We analyzed the genetic variants of 6 candidate genes and the gene deletion in complement factor H (CFH) and CFH-related genes, examined the prevalence of CFH autoantibodies and evaluated the genotype-phenotype relationship in 10 Japanese patients with aHUS. ...The …
We analyzed the genetic variants of 6 candidate genes and the gene deletion in complement factor H (CFH) and CFH-related genes …
Complement factor H gene associations with end-stage kidney disease in African Americans.
Bonomo JA, Palmer ND, Hicks PJ, Lea JP, Okusa MD, Langefeld CD, Bowden DW, Freedman BI. Bonomo JA, et al. Nephrol Dial Transplant. 2014 Jul;29(7):1409-14. doi: 10.1093/ndt/gfu036. Epub 2014 Feb 28. Nephrol Dial Transplant. 2014. PMID: 24586071 Free PMC article.
These results suggest that a subset of cases with ESKD clinically ascribed to the effects of hypertension or glomerulosclerosis actually have CFH-related forms of mesangial proliferative glomerulonephritis. Genetic testing may prove useful to identify the causes of …
These results suggest that a subset of cases with ESKD clinically ascribed to the effects of hypertension or glomerulosclerosis actually hav …