-
2
-
-
39349110015
-
Emergence of endemic serogroup W135 meningococcal disease associated with a high mortality rate in South Africa
-
von Gottberg A, du Plessis M, Cohen C, et al. Emergence of endemic serogroup W135 meningococcal disease associated with a high mortality rate in South Africa. Clin Infect Dis 2008;46:377-386. [http://dx.doi.org/10.1086/525260]
-
(2008)
Clin Infect Dis
, vol.46
, pp. 377-386
-
-
von Gottberg, A.1
du Plessis, M.2
Cohen, C.3
-
3
-
-
0023424916
-
Deficiency of the sixth component of complement and susceptibility to Neisseria meningitidis infections. Studies in ten families and five isolated cases
-
Orren A, Potter PC, Cooper R, du Toit E. Deficiency of the sixth component of complement and susceptibility to Neisseria meningitidis infections. Studies in ten families and five isolated cases. Immunology 1987;62:249-253.
-
(1987)
Immunology
, vol.62
, pp. 249-253
-
-
Orren, A.1
Potter, P.C.2
Cooper, R.3
du Toit, E.4
-
4
-
-
0026016383
-
Functionally active complement proteins C6 and C7 detected in C6-and C7-deficient individuals
-
Würzner R, Orren A, Potter P, et al. Functionally active complement proteins C6 and C7 detected in C6-and C7-deficient individuals. Clin Exp Immunol 1991;83:430-437. [http://dx.doi.org/10.1111/j.1365-2249.1991.tb05656.x]
-
(1991)
Clin Exp Immunol
, vol.83
, pp. 430-437
-
-
Würzner, R.1
Orren, A.2
Potter, P.3
-
5
-
-
0031784829
-
The molecular bases of C6 deficiency in the Western Cape, South Africa
-
Hobart MJ, Fernie BA, Fijen KAPM, Orren A. The molecular bases of C6 deficiency in the Western Cape, South Africa. Hum Genetics 1998;103:506-512. [http://dx.doi.org/10.1007/s004390050858]
-
(1998)
Hum Genetics
, vol.103
, pp. 506-512
-
-
Hobart, M.J.1
Fernie, B.A.2
Fijen, K.A.P.M.3
Orren, A.4
-
6
-
-
13344259991
-
Molecular bases for inherited human complement component C6 deficiency in two unrelated individuals
-
Nishizaka H, Horiuchi T, Zhu ZB, et al. Molecular bases for inherited human complement component C6 deficiency in two unrelated individuals. J Immunology 1996;156:2309-2315.
-
(1996)
J Immunology
, vol.156
, pp. 2309-2315
-
-
Nishizaka, H.1
Horiuchi, T.2
Zhu, Z.B.3
-
7
-
-
0031881824
-
Molecular defects leading to human complement component C6 deficiency in an African-American family
-
Zhu ZB, Totemchokchyakarn K, Atkinson TP, Volanakis JE. Molecular defects leading to human complement component C6 deficiency in an African-American family. Clin Exp Immunol 1998;111:91-96. [http://dx.doi.org/10.1046/j.1365-2249.1998.00455.x]
-
(1998)
Clin Exp Immunol
, vol.111
, pp. 91-96
-
-
Zhu, Z.B.1
Totemchokchyakarn, K.2
Atkinson, T.P.3
Volanakis, J.E.4
-
8
-
-
84870356044
-
Complement component 5 deficiency (C5D) in South Africa
-
Orren A, Owen EP, Potter PC, Leisegang F, Morgan BP, Wurzner R. Complement component 5 deficiency (C5D) in South Africa. Molecular Immunology 2011;48:1863.
-
(2011)
Molecular Immunology
, vol.48
, pp. 1863
-
-
Orren, A.1
Owen, E.P.2
Potter, P.C.3
Leisegang, F.4
Morgan, B.P.5
Wurzner, R.6
-
9
-
-
0025913102
-
Infectious diseases associated with complement deficiencies
-
Figueroa JE, Densen P. Infectious diseases associated with complement deficiencies. Clin Microbiol 1991;4:359-395
-
(1991)
Clin Microbiol
, vol.4
, pp. 359-395
-
-
Figueroa, J.E.1
Densen, P.2
-
10
-
-
84856386049
-
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, et al. 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. Clinical and Experimental Immunology 2012;167:459-471. [http://dx.doi.org/10.1111/j.1365-2249.2011.04525.x]
-
(2012)
Clinical and Experimental Immunology
, vol.167
, pp. 459-471
-
-
Orren, A.1
Owen, E.P.2
Henderson, H.E.3
-
11
-
-
0029062206
-
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, et al. 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. J Immunol 1995;154:5464-5471.
-
(1995)
J Immunol
, vol.154
, pp. 5464-5471
-
-
Wang, X.1
Fleischer, D.T.2
Whitehead, W.T.3
-
12
-
-
33846913468
-
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, et al. 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. Mol Immunol 2007;44:2756-2760.
-
(2007)
Mol Immunol
, vol.44
, pp. 2756-2760
-
-
Parham, K.L.1
Roberts, A.2
Thomas, A.3
-
13
-
-
0025913053
-
Blood dendritic cells carry terminal complement complexes on their cell surface as detected by newly developed neoepitope-specific monoclonal antibodies
-
PMID 1718850
-
Würzner R, Xu H, Franzke A, Schulze M, Peters JH, Götze O. Blood dendritic cells carry terminal complement complexes on their cell surface as detected by newly developed neoepitope-specific monoclonal antibodies. Immunology 1991;74:132-138. [PMID 1718850]
-
(1991)
Immunology
, vol.74
, pp. 132-138
-
-
Würzner, R.1
Xu, H.2
Franzke, A.3
Schulze, M.4
Peters, J.H.5
Götze, O.6
-
14
-
-
67349229266
-
Molecular Immunology. 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. Molecular Immunology. Molecular characterization of three new mutations causing C5 deficiency in two non-related families. Mol Immunol 2009;46:2340-2347.
-
(2009)
Mol Immunol
, vol.46
, pp. 2340-2347
-
-
López-Lera, A.1
Garrido, S.2
de la Cruz, R.M.3
Fontán, G.4
López-Trascasa, M.5
-
15
-
-
67349098522
-
Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability
-
Aguilar-Ramireza P, Reis ES, Floridoa MPC, et al. Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability. Mol Immunol 2009;46:2116-2123. [http://dx.doi.org/10.1016/j.molimm.2008.10.035]
-
(2009)
Mol Immunol
, vol.46
, pp. 2116-2123
-
-
Aguilar-Ramireza, P.1
Reis, E.S.2
Floridoa, M.P.C.3
-
16
-
-
0037932209
-
-
Statistics South Africa. Pretoria, Statistics South Africa,(accessed 11 April 2012)
-
Statistics South Africa. Census 2001. Pretoria, Statistics South Africa, 2003. http://www.statssa.gov.za/census01/html/default.asp (accessed 11 April 2012).
-
(2003)
Census 2001
-
-
-
17
-
-
33846680365
-
Meningococcal disease in South Africa, 1999-2002
-
Coulson GB, von Gottberg A, du Plessis M, Smith AM, de Gouvia L, Klugman KP. Meningococcal disease in South Africa, 1999-2002. Emerging Infect Diseases 2007;13:273-278. [http://dx.doi.org/10.3201/eid1302.051553]
-
(2007)
Emerging Infect Diseases
, vol.13
, pp. 273-278
-
-
Coulson, G.B.1
von Gottberg, A.2
du Plessis, M.3
Smith, A.M.4
de Gouvia, L.5
Klugman, K.P.6
-
18
-
-
79951812892
-
Distribution of factor H binding protein beyond serogroup B: Variation among five serogroups of invasive Neisseria meningitidis in South Africa
-
Kedibone MM, du Plessis M, von Gottberg A, et al. Distribution of factor H binding protein beyond serogroup B: Variation among five serogroups of invasive Neisseria meningitidis in South Africa. Vaccine 2011;29:2187-2192. [http://dx.doi.org/10.1016/j.vaccine.2010.11.072]
-
(2011)
Vaccine
, vol.29
, pp. 2187-2192
-
-
Kedibone, M.M.1
du Plessis, M.2
von Gottberg, A.3
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