129 related articles for article (PubMed ID: 22668955)
1. Complement component C5 and C6 mutation screening indicated in meningococcal disease in South Africa.
Owen EP; Leisegang F; Whitelaw A; Simpson J; Baker S; Würzner R; Potter P; Orren A
S Afr Med J; 2012 May; 102(6):525-7. PubMed ID: 22668955
[TBL] [Abstract][Full Text] [Related]
2. Complete deficiency of the sixth complement component (C6Q0), susceptibility to Neisseria meningitidis infections and analysis of the frequencies of C6Q0 gene defects in South Africans.
Orren A; Owen EP; Henderson HE; van der Merwe L; Leisegang F; Stassen C; Potter PC
Clin Exp Immunol; 2012 Mar; 167(3):459-71. PubMed ID: 22288589
[TBL] [Abstract][Full Text] [Related]
3. A complement C5 gene mutation, c.754G>A:p.A252T, is common in the Western Cape, South Africa and found to be homozygous in seven percent of Black African meningococcal disease cases.
Owen EP; Würzner R; Leisegang F; Rizkallah P; Whitelaw A; Simpson J; Thomas AD; Harris CL; Giles JL; Hellerud BC; Mollnes TE; Morgan BP; Potter PC; Orren A
Mol Immunol; 2015 Mar; 64(1):170-6. PubMed ID: 25534848
[TBL] [Abstract][Full Text] [Related]
4. Prevalence of mutations leading to complete C6 deficiency (C6Q0) in the Western Cape, South Africa and detection of novel mutations leading to C6Q0 in an Irish family.
Parham KL; Roberts A; Thomas A; Würzner R; Henderson HE; Potter PC; Morgan BP; Orren A
Mol Immunol; 2007 Apr; 44(10):2756-60. PubMed ID: 17257682
[TBL] [Abstract][Full Text] [Related]
5. Complement factor 5 (C5) p.A252T mutation is prevalent in, but not restricted to, sub-Saharan Africa: implications for the susceptibility to meningococcal disease.
Franco-Jarava C; Comas D; Orren A; Hernández-González M; Colobran R
Clin Exp Immunol; 2017 Aug; 189(2):226-231. PubMed ID: 28369827
[TBL] [Abstract][Full Text] [Related]
6. The molecular basis of C6 deficiency in the western Cape, South Africa.
Hobart MJ; Fernie BA; Fijen KA; Orren A
Hum Genet; 1998 Oct; 103(4):506-12. PubMed ID: 9856498
[TBL] [Abstract][Full Text] [Related]
7. High prevalence of complement component C6 deficiency among African-Americans in the south-eastern USA.
Zhu Z; Atkinson TP; Hovanky KT; Boppana SB; Dai YL; Densen P; Go RC; Jablecki JS; Volanakis JE
Clin Exp Immunol; 2000 Feb; 119(2):305-10. PubMed ID: 10632667
[TBL] [Abstract][Full Text] [Related]
8. [Hereditary complement C5 deficiency: study of 3 Tunisian adult cases and literature review].
Zerzri Y; Kallel-Sellami M; Abdelmalek R; Laadhar L; Ben Chaabane T; Makni S
Tunis Med; 2010 Apr; 88(4):269-76. PubMed ID: 20446263
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Deficiency of the sixth component of complement and susceptibility to Neisseria meningitidis infections: studies in 10 families and five isolated cases.
Orren A; Potter PC; Cooper RC; du Toit E
Immunology; 1987 Oct; 62(2):249-53. PubMed ID: 3679285
[TBL] [Abstract][Full Text] [Related]
11. Molecular defects leading to human complement component C6 deficiency in an African-American family.
Zhu ZB; Totemchokchyakarn K; Atkinson TP; Volanakis JE
Clin Exp Immunol; 1998 Jan; 111(1):91-6. PubMed ID: 9472666
[TBL] [Abstract][Full Text] [Related]
12. Invasive Meningococcal Disease Unraveling a Novel Mutation in the C5 Gene in a Portuguese Family.
Marujo F; Costa LC; Duarte R; Brito MJ; Cordeiro A; Neves C; Neves JF
Pediatr Infect Dis J; 2019 Apr; 38(4):416-418. PubMed ID: 30882736
[TBL] [Abstract][Full Text] [Related]
13. Combined complete C5 and partial C4 deficiency in humans: clinical consequences and complement-mediated functions in vitro.
Gianella-Borradori A; Borradori L; Schneider PM; Gautier E; Späth PJ
Clin Immunol Immunopathol; 1990 Apr; 55(1):41-55. PubMed ID: 2306879
[TBL] [Abstract][Full Text] [Related]
14. Inherited human complement C5 deficiency. Nonsense mutations in exons 1 (Gln1 to Stop) and 36 (Arg1458 to Stop) and compound heterozygosity in three African-American families.
Wang X; Fleischer DT; Whitehead WT; Haviland DL; Rosenfeld SI; Leddy JP; Snyderman R; Wetsel RA
J Immunol; 1995 May; 154(10):5464-71. PubMed ID: 7730648
[TBL] [Abstract][Full Text] [Related]
15. [Recurrent meningococcal meningitis associated with complement C6 deficiency (author's transl)].
Avril MF; Lebas J; Autran B; Modai J
Nouv Presse Med; 1981 Oct; 10(37):3057-9. PubMed ID: 7290963
[TBL] [Abstract][Full Text] [Related]
16. Molecular characterization of three new mutations causing C5 deficiency in two non-related families.
López-Lera A; Garrido S; de la Cruz RM; Fontán G; López-Trascasa M
Mol Immunol; 2009 Jul; 46(11-12):2340-7. PubMed ID: 19414197
[TBL] [Abstract][Full Text] [Related]
17. Terminal complement component deficiencies in Japan.
Fukumori Y; Horiuchi T
Exp Clin Immunogenet; 1998; 15(4):244-8. PubMed ID: 10072634
[TBL] [Abstract][Full Text] [Related]
18. Meningococcal meningitis in familial deficiency of the fifth component of complement.
Peter G; Weigert MB; Bissel AR; Gold R; Kreutzer D; McLean RH
Pediatrics; 1981 Jun; 67(6):882-6. PubMed ID: 6785713
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Novel pathogenic mutations identified in the first Chinese pedigree of complete C6 deficiency.
Li PH; Wong WW; Leung EN; Lau CS; Au E
Clin Transl Immunology; 2020; 9(7):e1148. PubMed ID: 32670577
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
