Literature DB >> 2231209

Association of Henoch-Schönlein purpura glomerulonephritis with C4B deficiency.

B H Ault1, F B Stapleton, M L Rivas, F B Waldo, S Roy, R H McLean, J A Bin, R J Wyatt.   

Abstract

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Year:  1990        PMID： 2231209     DOI： 10.1016/s0022-3476(05)83336-0

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  6 in total

1.  A unique recombination event resulting in a C4A*Q0,C4B*Q0 double null haplotype.

Authors:  M B Fasano; J A Winkelstein; T LaRosa; W B Bias; R H McLean
Journal:  J Clin Invest       Date:  1992-10       Impact factor: 14.808

2.  Defective prevention of immune precipitation in autoimmune diseases is independent of C4A*Q0.

Authors:  G J Arason; R Kolka; A B Hreidarsson; H Gudjonsson; P M Schneider; L Fry; A Arnason
Journal:  Clin Exp Immunol       Date:  2005-06       Impact factor: 4.330

3.  Familial C4B deficiency and immune complex glomerulonephritis.

Authors:  K Soto; Y L Wu; A Ortiz; S R Aparício; C Y Yu
Journal:  Clin Immunol       Date:  2010-07-02       Impact factor: 3.969

Review 4.  Complement and glomerulonephritis--an update.

Authors:  R H McLean
Journal:  Pediatr Nephrol       Date:  1993-04       Impact factor: 3.714

5.  Real-time PCR quantification of human complement C4A and C4B genes.

Authors:  Agnes Szilagyi; Bernadett Blasko; Denes Szilassy; George Fust; Maria Sasvari-Szekely; Zsolt Ronai
Journal:  BMC Genet       Date:  2006-01-10       Impact factor: 2.797

Review 6.  Pathogenesis of Henoch-Schönlein purpura nephritis.

Authors:  Keith K Lau; Hitoshi Suzuki; Jan Novak; Robert J Wyatt
Journal:  Pediatr Nephrol       Date:  2009-06-13       Impact factor: 3.714
  6 in total

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