Lack of Association between the HLA-A10 (A25), B18 and C2° Haplotype and Anaphylactoid Purpura (AP)
Author:
Publisher
Wiley
Subject
Genetics,Biochemistry,Immunology,General Medicine,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0039.1980.tb00887.x/fullpdf
Reference20 articles.
1. Complement deficiency states;Agnello;Medicine (Baltimore),1978
2. Die klinische Bedeutung der Gewebsantigene (HL-A) des Menschen;Albert;Munch, med. Wscbr,1976
3. Biological Amplification Systems in Immunology
4. Biosynthetic defect in monocytes from human beings with genetic deficiency of the second component of complement;Einstein;New Engl. J.Med,1975
5. Evidence for linkage between HL-A histocompatibility genes and those involved in the synthesis of the second component of complement;Fu;J. exp.Med,1974
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Henoch-Schönlein Purpura in Children: Report of 100 Patients and Review of the Literature;Medicine;1999-11
2. Recurrent post-infective Henoch-Schönlein syndrome: A genetic influence related to HLA B35?;Journal of Infection;1992-09
3. Allergy;HLA and Disease Associations;1985
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