92 related articles for article (PubMed ID: 3341877)
1. C5 deficiency and meningitis in a Swiss family.
Gianella-Borradori A; Borradori L; Späth P
Arch Intern Med; 1988 Mar; 148(3):754. PubMed ID: 3341877
[No Abstract] [Full Text] [Related]
2. Meningococcal disease in congenital absence of the fifth component of complement.
Nielsen HE; Koch C
Scand J Infect Dis; 1987; 19(6):635-9. PubMed ID: 3441749
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. C5 deficiency in a white family.
Boelaert J; Joos R; Criel A; Van Landuyt HW; Daha MR
Arch Intern Med; 1985 Jul; 145(7):1333. PubMed ID: 4015289
[No Abstract] [Full Text] [Related]
5. 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]
6. [Homozygotic C5 deficiency disclosed by purulent Neisseria meningitidis meningitis].
Cesbron JY; Maillet F; Valance J; Langlet N; Kazatchkine M
Presse Med; 1985 Dec; 14(45):2287-9. PubMed ID: 2935813
[TBL] [Abstract][Full Text] [Related]
7. [Hereditary C5 deficiency and recurrent Neisseria meningitidis meningitis].
Ducret F; Decoux M; Pointet P; Lambert C; Grosperrin E; Sédaillan A
Rev Med Interne; 1988; 9(5):534-7. PubMed ID: 3067301
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Recurrent bacterial meningitis due to genetic deficiencies of terminal complement components (C5 and C6).
Haeney MR; Ball AP; Thompson RA
Immunobiology; 1980; 158(1-2):101-6. PubMed ID: 7193645
[No Abstract] [Full Text] [Related]
10. [2 families with meningococcal infection and a hereditary disorder of the 5th component of the complement system].
Fijen CA; Kuijper EJ; Lindeboom SF; van Os J; van Putten JP
Ned Tijdschr Geneeskd; 1989 Sep; 133(36):1796-800. PubMed ID: 2682274
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Chronic meningococcal meningitis. An association with C5 deficiency.
Rosen MS; Lorber B; Myers AR
Arch Intern Med; 1988 Jun; 148(6):1441-2. PubMed ID: 3132125
[TBL] [Abstract][Full Text] [Related]
13. [The association between deficiency of terminal complement components and the occurrence of meningococcal meningitis].
Nishizaki M
Fukuoka Igaku Zasshi; 1992 May; 83(5):201-8. PubMed ID: 1612549
[TBL] [Abstract][Full Text] [Related]
14. [Recurring meningococcal meningitis in hereditary C 5 deficiency].
Hildenhagen O; Bitter-Suermann D
Dtsch Med Wochenschr; 1985 Sep; 110(39):1498-501. PubMed ID: 3928316
[TBL] [Abstract][Full Text] [Related]
15. [Recurring meningococcemia and C5 deficiency].
Ayensa C; Agud J; Gómez F; Echevarría MI
Med Clin (Barc); 1985 Mar; 84(11):463. PubMed ID: 3990415
[No 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. [Complement protein hereditary deficits during purulent meningitis: study of 61 adult Tunisian patients].
Kallel-Sellami M; Abdelmalek R; Zerzeri Y; Laadhar L; Blouin J; Zitouni M; Bacchi VF; Ben Chaabene T; Makni S
Arch Inst Pasteur Tunis; 2006; 83(1-4):25-34. PubMed ID: 19388594
[TBL] [Abstract][Full Text] [Related]
18. C5 complement deficiency in a Spanish family. Molecular characterization of the double mutation responsible for the defect.
Delgado-Cerviño E; Fontán G; López-Trascasa M
Mol Immunol; 2005 Jan; 42(1):105-11. PubMed ID: 15488949
[TBL] [Abstract][Full Text] [Related]
19. Novel Mutations Causing C5 Deficiency in Three North-African Families.
Colobran R; Franco-Jarava C; Martín-Nalda A; Baena N; Gabau E; Padilla N; de la Cruz X; Pujol-Borrell R; Comas D; Soler-Palacín P; Hernández-González M
J Clin Immunol; 2016 May; 36(4):388-96. PubMed ID: 27026170
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
