Literature DB >> 2656080

Frequency of complement deficiencies in man, disease associations and chromosome assignment of complement genes and linkage groups. A summary of the data from the literature.

G Hauptmann1.   

Abstract

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Year:  1989        PMID： 2656080     DOI： 10.1159/000463077

Source DB:  PubMed          Journal:  Complement Inflamm        ISSN： 1012-8204


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  5 in total

1.  Prevalence of hereditary properdin, C7 and C8 deficiencies in patients with meningococcal infections.

Authors:  M Schlesinger; Z Nave; Y Levy; P E Slater; Z Fishelson
Journal:  Clin Exp Immunol       Date:  1990-09       Impact factor: 4.330

2.  Molecular defects of the C7 gene in two patients with complement C7 deficiency.

Authors:  Sonia Barroso; Claudine Rieubland; Antonia José álvarez; Margarita López-Trascasa; Pierre-Alexandre Bart; Antonio Núñez-Roldán; Berta Sánchez
Journal:  Immunology       Date:  2006-06       Impact factor: 7.397

3.  Molecular heterogeneity in deficiency of complement protein C2 type I.

Authors:  X Wang; A Circolo; M L Lokki; P G Shackelford; R A Wetsel; H R Colten
Journal:  Immunology       Date:  1998-02       Impact factor: 7.397

4.  Extensive genetic polymorphism in the human tumor necrosis factor region and relation to extended HLA haplotypes.

Authors:  C V Jongeneel; L Briant; I A Udalova; A Sevin; S A Nedospasov; A Cambon-Thomsen
Journal:  Proc Natl Acad Sci U S A       Date:  1991-11-01       Impact factor: 11.205

5.  Combined total deficiency of C7 and C4B with systemic lupus erythematosus (SLE).

Authors:  O G Segurado; A A Arnaiz-Villena; P Iglesias-Casarrubios; J Martinez-Laso; J L Vicario; G Fontan; M Lopez-Trascasa
Journal:  Clin Exp Immunol       Date:  1992-03       Impact factor: 4.330
  5 in total

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