Renin-angiotensin system gene polymorphisms: Association with susceptibility to Henoch-Schonlein purpura and renal involvement

Clinical Rheumatology

Volumn 25, Issue 6, 2006, Pages 861-865

  Özkaya, Ozan ^a,b   Söylemezoǧlu, Oǧuz ^a   Gönen, Sevim ^a   Misirlioǧolu, Müge ^a   Tuncer, Serdar ^a   Kalman, Süleyman ^a   Buyan, Necla ^a   Hasanoǧlu, Enver ^a  

^a GAZI UNIVERSITY   (Turkey)

^b ONDOKUZ MAYIS UNIVERSITY   (Turkey)

Author keywords

Children; Gene; Henoch Sch nlein purpura; Polymorphism; Renin angiotensin system

Indexed keywords

ANGIOTENSIN 1 RECEPTOR; ANGIOTENSINOGEN; CORTICOSTEROID; CYCLOPHOSPHAMIDE; DIPEPTIDYL CARBOXYPEPTIDASE; DNA; METHYLPREDNISOLONE; PREDNISONE;

ADOLESCENT; ANAPHYLACTOID PURPURA; ARTICLE; CHILD; CONFIDENCE INTERVAL; CONTROLLED STUDY; CORRELATION ANALYSIS; DISEASE ASSOCIATION; DISEASE SEVERITY; DNA EXTRACTION; DRUG PULSE THERAPY; FEMALE; GENE DELETION; GENE FREQUENCY; GENE INSERTION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; GENOTYPE; HIGH RISK PATIENT; HUMAN; KIDNEY BIOPSY; MAJOR CLINICAL STUDY; MALE; NEPHRITIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEINURIA; RENIN ANGIOTENSIN ALDOSTERONE SYSTEM; RISK ASSESSMENT;

ADOLESCENT; ALANINE; ANGIOTENSINOGEN; CHILD; CHILD, PRESCHOOL; CYSTEINE; DNA TRANSPOSABLE ELEMENTS; FEMALE; GENE DELETION; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; KIDNEY DISEASES; MALE; METHIONINE; NEPHROTIC SYNDROME; PEPTIDYL-DIPEPTIDASE A; POLYMORPHISM, GENETIC; PROTEINURIA; PURPURA, SCHOENLEIN-HENOCH; RECEPTOR, ANGIOTENSIN, TYPE 1; RENIN-ANGIOTENSIN SYSTEM; SEVERITY OF ILLNESS INDEX; THREONINE;

EID: 33749182222     PISSN: 07703198     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10067-006-0207-4     Document Type: Article

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