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Items: 1 to 20 of 88

1.
Mannan-binding lectin may facilitate the clearance of circulating immune complexes – implications from a study on C2-deficient individuals
S Saevarsdottir, K Steinsson, B R Ludviksson, G Grondal, H Valdimarsson
Clin Exp Immunol. 2007 May; 148(2): 248–253. doi: 10.1111/j.1365-2249.2007.03349.x
PMCID:
PMC1868874
AbstractArticlePDF–186K
2.
Hereditary deficiency of the second component of complement (C2) in man: correlation of C2 haemolytic activity with immunochemical measurements of C2 protein
S. Ruddy, M. R. Klemperer, F. S. Rosen, K. F. Austen, J. Kumate
Immunology. 1970 Jun; 18(6): 943–954.
PMCID:
PMC1455728
SummaryPage BrowsePDF–1.4M
3.
Simultaneous occurrence of hereditary C6 and C2 deficiency in a French-Canadian family.
J M Delâge, G Lehner-Netsch, R Lafleur, J Simard, G Brun, E Prochazka
Immunology. 1979 Jun; 37(2): 419–428.
PMCID:
PMC1457517
SummaryPage BrowsePDF–1.2M
4.
Hypocomplementaemia due to a genetic deficiency of beta 1H globulin.
R A Thompson, M H Winterborn
Clin Exp Immunol. 1981 Oct; 46(1): 110–119.
PMCID:
PMC1536333
SummaryPage BrowsePDF–1.2M
5.
Renal transplantation in a patient with hereditary deficiency of the second component of complement.
H J Zeitz, A Gewurz, O Jonasson, W P Geis, H Gewurz
Clin Exp Immunol. 1981 Nov; 46(2): 420–424.
PMCID:
PMC1536388
SummaryPage BrowsePDF–607K
6.
Familial C1q deficiency associated with renal and cutaneous disease.
F Leyva-Cobián, I Moneo, F Mampaso, M Sánchez-Bayle, J L Ecija, A Bootello
Clin Exp Immunol. 1981 Apr; 44(1): 173–180.
PMCID:
PMC1537222
SummaryPage BrowsePDF–1.2M
7.
C3 metabolism in a patient with deficiency of the second component of complement (C2) and discoid lupus erythematosus.
J H Wild, N J Zvaifler, H J Müller-Eberhard, C B Wilson
Clin Exp Immunol. 1976 May; 24(2): 238–248.
PMCID:
PMC1538409
SummaryPage BrowsePDF–1.8M
8.
Heterogeneity of the clinical syndrome in patients with systemic lupus erythematosus and genetic deficiency of the second complement component.
R I Rynes, R E Urizar, R J Pickering
Clin Exp Immunol. 1978 Apr; 32(1): 59–68.
PMCID:
PMC1541290
SummaryPage BrowsePDF–2.7M
9.
Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility.
A H Fielder, M J Walport, J R Batchelor, R I Rynes, C M Black, I A Dodi, G R Hughes
Br Med J (Clin Res Ed) 1983 Feb 5; 286(6363): 425–428. doi: 10.1136/bmj.286.6363.425
PMCID:
PMC1546768
SummaryPage BrowsePDF–839K
10.
Homozygous deficiency of the second component of complement presenting with recurrent bacterial meningitis.
Y H Thong, D A Simpson, H J Müller-Eberhard
Arch Dis Child. 1980 Jun; 55(6): 471–473. doi: 10.1136/adc.55.6.471
PMCID:
PMC1626939
SummaryPage BrowsePDF–373K
11.
Immunoglobulins and complement factor C4 in adult rhinosinusitis
M Seppänen, J Suvilehto, M-L Lokki, I-L Notkola, A Järvinen, H Jarva, I Seppälä, O Tahkokallio, H Malmberg, S Meri, V Valtonen
Clin Exp Immunol. 2006 Aug; 145(2): 219–227. doi: 10.1111/j.1365-2249.2006.03134.x
PMCID:
PMC1809671
AbstractArticlePDF–130K
12.
Cleavage of the second component of complement by plasma proteases: implications in hereditary C1-inhibitor deficiency.
M A Smith, M A Kerr
Immunology. 1985 Nov; 56(3): 561–570.
PMCID:
PMC1453753
SummaryPage BrowsePDF–1.5M
13.
Lack of evidence of a specific role for C4A gene deficiency in determining disease susceptibility among C4-deficient patients with systemic lupus erythematosus (SLE)
M -A Dragon-Durey, N Rougier, J -P Clauvel, S Caillat-Zucman, P Remy, L Guillevin, F Liote, J Blouin, F Ariey, B U Lambert, M D Kazatchkine, L Weiss
Clin Exp Immunol. 2001 Jan; 123(1): 133–139. doi: 10.1046/j.1365-2249.2001.01438.x
PMCID:
PMC1905972
AbstractArticlePDF–98K
14.
Immune complex processing in C1q-deficient mice
J T Nash, P R Taylor, M Botto, P J Norsworthy, K A Davies, M J Walport
Clin Exp Immunol. 2001 Feb; 123(2): 196–202. doi: 10.1046/j.1365-2249.2001.01459.x
PMCID:
PMC1905984
AbstractArticlePDF–162K
15.
IN VITRO STUDIES OF COMPLEMENT FUNCTION IN SERA OF C4-DEFICIENT GUINEA PIGS
Michael M. Frank, Joseph May, Thelma Gaither, Leonard Ellman
J Exp Med. 1971 Jul 1; 134(1): 176–187. doi: 10.1084/jem.134.1.176
PMCID:
PMC2139026
SummaryPDF–612K
16.
EVIDENCE FOR LINKAGE BETWEEN HL-A HISTOCOMPATIBILITY GENES AND THOSE INVOLVED IN THE SYNTHESIS OF THE SECOND COMPONENT OF COMPLEMENT
S. M. Fu, H. G. Kunkel, H. P. Brusman, F. H. Allen, Jr., M. Fotino
J Exp Med. 1974 Oct 1; 140(4): 1108–1111. doi: 10.1084/jem.140.4.1108
Correction in:
J Exp Med. 1974 Nov 30; 140(6): 1437.
PMCID:
PMC2139628
SummaryPDF–200K
17.
T Cell–dependent Immune Response in C1q-deficient Mice: Defective Interferon γ Production by Antigen-specific T Cells
Antony J. Cutler, Marina Botto, Dominic van Essen, Roberta Rivi, Kevin A. Davies, David Gray, Mark J. Walport
J Exp Med. 1998 Jun 1; 187(11): 1789–1797. doi: 10.1084/jem.187.11.1789
PMCID:
PMC2212306
AbstractArticlePDF–6.4M
18.
Transgenic Mice Overexpressing the Complement Inhibitor Crry as a Soluble Protein Are Protected from Antibody-induced Glomerular Injury
Richard J. Quigg, Chun He, Alice Lim, Dawn Berthiaume, Jessy J. Alexander, Damian Kraus, V. Michael Holers
J Exp Med. 1998 Oct 5; 188(7): 1321–1331. doi: 10.1084/jem.188.7.1321
PMCID:
PMC2212499
AbstractArticlePDF–1.5M
19.
Depressed activation of the lectin pathway of complement in hereditary angioedema
L Varga, G Széplaki, J Laki, A Kocsis, K Kristóf, P Gál, Z Bajtay, J Wieslander, M R Daha, P Garred, H O Madsen, G Füst, H Farkas
Clin Exp Immunol. 2008 Jul; 153(1): 68–74. doi: 10.1111/j.1365-2249.2008.03671.x
PMCID:
PMC2432099
AbstractArticlePDF–179K
20.
Complement 4 phenotypes and genotypes in Brazilian patients with classical 21-hydroxylase deficiency
G Guerra-Junior, A Sevciovic Grumach, S H Valente de Lemos-Marini, M Kirschfink, A Condino Neto, M de Araujo, M Palandi De Mello
Clin Exp Immunol. 2009 Feb; 155(2): 182–188. doi: 10.1111/j.1365-2249.2008.03838.x
PMCID:
PMC2675248
AbstractArticlePDF–212K

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