139 related articles for article (PubMed ID: 19414197)
1. 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]
2. 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]
3. The role of complement in anti-bacterial defence.
D'Amelio R; Biselli R
Ann Ital Med Int; 1994; 9(3):173-7. PubMed ID: 7946895
[TBL] [Abstract][Full Text] [Related]
4. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
5. Complement component C6 deficiency in a Spanish family: implications for clinical and molecular diagnosis.
Moya-Quiles MR; Bernardo-Pisa MV; Martínez P; Gimeno L; Bosch A; Salgado G; Martínez-Banaclocha H; Eguia J; Campillo JA; Muro M; Vidal-Bugallo JB; Alvarez-López MR; García-Alonso AM
Gene; 2013 May; 521(1):204-6. PubMed ID: 23537992
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. C5 complement deficiency in a Saudi family, molecular characterization of mutation and literature review.
Arnaout R; Al Shorbaghi S; Al Dhekri H; Al-Mousa H; Al Ghonaium A; Al Saud B; Al Muhsen S; Al Baik L; Hawwari A
J Clin Immunol; 2013 May; 33(4):871-5. PubMed ID: 23371790
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [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]
10. 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]
11. [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]
12. [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]
13. 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]
14. [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]
15. 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]
16. 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]
17. [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]
18. [Meningococcal meningitis in isolated familial deficiency of the 7th complement component, C7].
Straub PW; Späth P
Schweiz Med Wochenschr; 1986 May; 116(21):699-702. PubMed ID: 3726502
[TBL] [Abstract][Full Text] [Related]
19. [A case of C5 deficiency with polyarthritis].
Mimori M; Yamauchi I; Nishimura Y; Takada K; Inai S
Rinsho Byori; 1992 Jun; 40(6):660-4. PubMed ID: 1513039
[TBL] [Abstract][Full Text] [Related]
20. C8 beta subunit deficiency in a patient with recurrent neisserial infections.
Fontana L; Tedesco F; De Carolis C; Roncelli L; Teggi A; Paffetti A; Perricone R
Ric Clin Lab; 1987; 17(1):19-25. PubMed ID: 3109005
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]