The genetics of Henoch-Schönlein purpura: A systematic review and meta-analysis

Rheumatology International

Volumn 33, Issue 6, 2013, Pages 1387-1395

  He, Xuelian ^a   Yu, Chunhua ^a   Zhao, Peiwei ^a   Ding, Yan ^a   Liang, Xiaohui ^c   Zhao, Yulan ^b   Yue, Xin ^a   Wu, Yanxiang ^a   Yin, Wei ^a  

^a Wuhan Children's Hospital   (China)

^b EAST CHINA NORMAL UNIVERSITY   (China)

^c WUHAN UNIVERSITY   (China)

Author keywords

Genetic association studies; Genetic polymorphisms; Henoch Sch nlein purpura

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); ANGIOTENSINOGEN; CYTOTOXIC T LYMPHOCYTE ANTIGEN 4; DIPEPTIDYL CARBOXYPEPTIDASE; ENDOTHELIAL LEUKOCYTE ADHESION MOLECULE 1; ENDOTHELIAL NITRIC OXIDE SYNTHASE; HLA A ANTIGEN; HLA B ANTIGEN; HLA DQA1 ANTIGEN; HLA DRB1 ANTIGEN; INTERCELLULAR ADHESION MOLECULE 1; INTERLEUKIN 8; NON RECEPTOR PROTEIN TYROSINE PHOSPHATASE 22; RANTES; TOLL LIKE RECEPTOR 2; TOLL LIKE RECEPTOR 4; VASCULOTROPIN;

ANAPHYLACTOID PURPURA; COMPLEMENT SYSTEM; DISEASE SEVERITY; FAMILIAL MEDITERRANEAN FEVER; GENE DELETION; GENE FUNCTION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC REGULATION; GENETIC SUSCEPTIBILITY; HLA SYSTEM; HUMAN; INFLAMMATION; META ANALYSIS; PRIORITY JOURNAL; RENIN ANGIOTENSIN ALDOSTERONE SYSTEM; REVIEW; SYSTEMATIC REVIEW;

CYTOKINES; GENES, MHC CLASS II; GENOME-WIDE ASSOCIATION STUDY; HUMANS; PEPTIDYL-DIPEPTIDASE A; POLYMORPHISM, GENETIC; PURPURA, SCHOENLEIN-HENOCH;

EID: 84878676796     PISSN: 01728172     EISSN: 1437160X     Source Type: Journal    
DOI: 10.1007/s00296-012-2661-4     Document Type: Review

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