These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
24. Compound heterozygous mutations in the C6 gene of a child with recurrent infections. Westra D; Kurvers RA; van den Heuvel LP; Würzner R; Hoppenreijs EP; van der Flier M; van de Kar NC; Warris A Mol Immunol; 2014 Apr; 58(2):201-5. PubMed ID: 24378253 [TBL] [Abstract][Full Text] [Related]
26. Prophylaxis against Neisseria meningitidis infections and antibody responses in patients with deficiency of the sixth component of complement. Potter PC; Frasch CE; van der Sande WJ; Cooper RC; Patel Y; Orren A J Infect Dis; 1990 May; 161(5):932-7. PubMed ID: 2109021 [TBL] [Abstract][Full Text] [Related]
27. The human complement C9 gene: identification of two mutations causing deficiency and revision of the gene structure. Witzel-Schlömp K; Späth PJ; Hobart MJ; Fernie BA; Rittner C; Kaufmann T; Schneider PM J Immunol; 1997 May; 158(10):5043-9. PubMed ID: 9144525 [TBL] [Abstract][Full Text] [Related]
28. Absence of the sixth component of complement in a patient with repeated episodes of meningococcal meningitis. Lim D; Gewurz A; Lint TF; Ghaze M; Sepheri B; Gewurz H J Pediatr; 1976 Jul; 89(1):42-7. PubMed ID: 819642 [TBL] [Abstract][Full Text] [Related]
29. Recurrent meningococcal meningitis with complement 6 (C6) deficiency: A case report. Bae JY; Ham A; Choi HJ; Kim CJ Medicine (Baltimore); 2020 May; 99(21):e20362. PubMed ID: 32481330 [TBL] [Abstract][Full Text] [Related]
30. Genetic detection of the silent allele (*Q0) in hereditary deficiencies of the human complement C6, C7, and C9 components. Alvarez V; Coto E; Setién F; Spath PJ; López-Larrea C Am J Med Genet; 1995 Feb; 55(4):408-13. PubMed ID: 7762578 [TBL] [Abstract][Full Text] [Related]
31. Association of a 12.5-kilobase allele of the MspI restriction fragment length polymorphism of the C6 gene in patients with total deficiency of the sixth component of complement. Potter PC; Warburton C; Würzner R; Orren A; Di Scipio R Exp Clin Immunogenet; 1993; 10(1):38-44. PubMed ID: 7691111 [TBL] [Abstract][Full Text] [Related]
32. Recurrent bacterial meningitis in patients with genetic defects of terminal complement components. Haeney MR; Thompson RA; Faulkner J; Mackintosh P; Ball AP Clin Exp Immunol; 1980 Apr; 40(1):16-24. PubMed ID: 7389212 [TBL] [Abstract][Full Text] [Related]
33. C6 haplotypes: associations of a Dde I site polymorphism to complement deficiency genes and the Msp I restriction fragment length polymorphism (RFLP). Fernie BA; Hobart MJ; Delbridge G; Potter PC; Orren A; Lachmann PJ Clin Exp Immunol; 1994 Feb; 95(2):351-6. PubMed ID: 7508350 [TBL] [Abstract][Full Text] [Related]
34. Recurrent meningococcal meningitis with absence of the sixth component of complement: an evaluation of underlying immunologic mechanisms. Vogler LB; Newman SL; Stroud RM; Johnston RB Pediatrics; 1979 Oct; 64(4):465-7. PubMed ID: 492812 [TBL] [Abstract][Full Text] [Related]
35. [Complement terminal fraction deficiency revealed at first invasive meningococcal infection]. de Marcellus C; Taha MK; Gaudelus J; Fremeaux-Bacchi V; de Pontual L; Guiddir T Arch Pediatr; 2015 Mar; 22(3):296-9. PubMed ID: 25534556 [TBL] [Abstract][Full Text] [Related]
36. Neisseria meningitidis. Early treatment and complement deficiency. Vega C; Quinby PM J Ky Med Assoc; 1994 Jun; 92(6):227-9. PubMed ID: 8051497 [No Abstract] [Full Text] [Related]
37. Genetic control of C6 polymorphism and C6 deficiency in rabbits. Goldman MB; Cohen C; Stronski K; Bangalore S; Goldman JN J Immunol; 1982 Jan; 128(1):43-8. PubMed ID: 6172488 [TBL] [Abstract][Full Text] [Related]
38. [Deficiency of the 6th component of complement. Recurrent meningococcal and streptococcal meningitis]. Vincent D; Zemrag S; Rancurel G; Buge A Rev Med Interne; 1988; 9(1):93-6. PubMed ID: 3285426 [TBL] [Abstract][Full Text] [Related]
39. Molecular, genetic, and functional analysis of homozygous C8 beta-chain deficiency in two siblings. Kotnik V; Luznik-Bufon T; Schneider PM; Kirschfink M Immunopharmacology; 1997 Dec; 38(1-2):215-21. PubMed ID: 9476133 [TBL] [Abstract][Full Text] [Related]
40. Combined hereditary deficiency of the sixth component of complement and factor VIII coagulant activity in a Dutch family. Daha MR; Bertina RM; Thompson J; Kauffmann RH; Nicholson-Weller A; Veltkamp JJ; Briët E Clin Exp Immunol; 1982 Jun; 48(3):733-8. PubMed ID: 6811172 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]