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For: Taylor C. Complement factor H and the haemolytic uraemic syndrome. The Lancet 2001;358:1200-2. [DOI: 10.1016/s0140-6736(01)06339-5] [Cited by in Crossref: 37] [Cited by in F6Publishing: 9] [Article Influence: 1.8] [Reference Citation Analysis]
Number Citing Articles
1 Neumann HP, Salzmann M, Bohnert-Iwan B, Mannuelian T, Skerka C, Lenk D, Bender BU, Cybulla M, Riegler P, Königsrainer A, Neyer U, Bock A, Widmer U, Male DA, Franke G, Zipfel PF. Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries. J Med Genet 2003;40:676-81. [PMID: 12960213 DOI: 10.1136/jmg.40.9.676] [Cited by in Crossref: 153] [Cited by in F6Publishing: 147] [Article Influence: 8.1] [Reference Citation Analysis]
2 Cheong HI, Lee BS, Kang HG, Hahn H, Suh KS, Ha IS, Choi Y. Attempted treatment of factor H deficiency by liver transplantation. Pediatr Nephrol 2004;19:454-8. [PMID: 14986080 DOI: 10.1007/s00467-003-1371-2] [Cited by in Crossref: 61] [Cited by in F6Publishing: 52] [Article Influence: 3.4] [Reference Citation Analysis]
3 Oppermann M, Manuelian T, Józsi M, Brandt E, Jokiranta TS, Heinen S, Meri S, Skerka C, Götze O, Zipfel PF. The C-terminus of complement regulator Factor H mediates target recognition: evidence for a compact conformation of the native protein. Clin Exp Immunol 2006;144:342-52. [PMID: 16634809 DOI: 10.1111/j.1365-2249.2006.03071.x] [Cited by in Crossref: 121] [Cited by in F6Publishing: 118] [Article Influence: 7.6] [Reference Citation Analysis]
4 Kim S, Park E, Min SI, Yi NJ, Ha J, Ha IS, Cheong HI, Kang HG. Kidney Transplantation in Patients with Atypical Hemolytic Uremic Syndrome due to Complement Factor H Deficiency: Impact of Liver Transplantation. J Korean Med Sci 2018;33:e4. [PMID: 29215813 DOI: 10.3346/jkms.2018.33.e4] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
5 Zheng XL, Sadler JE. Pathogenesis of thrombotic microangiopathies. Annu Rev Pathol 2008;3:249-77. [PMID: 18215115 DOI: 10.1146/annurev.pathmechdis.3.121806.154311] [Cited by in Crossref: 139] [Cited by in F6Publishing: 106] [Article Influence: 9.9] [Reference Citation Analysis]
6 Hegasy GA, Manuelian T, Hogasen K, Jansen JH, Zipfel PF. The molecular basis for hereditary porcine membranoproliferative glomerulonephritis type II: point mutations in the factor H coding sequence block protein secretion. Am J Pathol 2002;161:2027-34. [PMID: 12466119 DOI: 10.1016/S0002-9440(10)64481-1] [Cited by in Crossref: 60] [Cited by in F6Publishing: 14] [Article Influence: 3.2] [Reference Citation Analysis]
7 Clark SJ, Bishop PN. Role of Factor H and Related Proteins in Regulating Complement Activation in the Macula, and Relevance to Age-Related Macular Degeneration. J Clin Med 2015;4:18-31. [PMID: 25729613 DOI: 10.3390/jcm4010018] [Cited by in Crossref: 27] [Cited by in F6Publishing: 26] [Article Influence: 3.9] [Reference Citation Analysis]
8 Manuelian T, Hellwage J, Meri S, Caprioli J, Noris M, Heinen S, Jozsi M, Neumann HP, Remuzzi G, Zipfel PF. Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome. J Clin Invest. 2003;111:1181-1190. [PMID: 12697737 DOI: 10.1172/jci16651] [Cited by in Crossref: 217] [Cited by in F6Publishing: 113] [Article Influence: 11.4] [Reference Citation Analysis]
9 Sethi SK, Marie-Agnes DD, Thaker N, Hari P, Bagga A. Hemolytic uremic syndrome due to homozygous factor H deficiency. Clin Exp Nephrol 2009;13:526-30. [PMID: 19568827 DOI: 10.1007/s10157-009-0205-3] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 0.4] [Reference Citation Analysis]