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Volumn 12, Issue 8, 2005, Pages 1232-1236

Hereditary angioneurotic edema: A case report in a 3-year-old child;Œdème angioneurotique héréditaire: À propos d'une observation chez un enfant de trois ans

Author keywords

Angioneurotic edema; Child; Complement 1 inactivators, therapeutic use; Dyspnea; Hereditary diseases; Tranexamic acid, therapeutic use

Indexed keywords

ADRENALIN; ANAPEN; METHYLPREDNISOLONE; TRANEXAMIC ACID; ADRENERGIC RECEPTOR STIMULATING AGENT; ANTIFIBRINOLYTIC AGENT; ANTIINFLAMMATORY AGENT; COMPLEMENT COMPONENT C1S INHIBITOR;

EID: 22944441277     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.arcped.2005.03.052     Document Type: Article
Times cited : (9)

References (10)
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    • A. Agostini, and M. Cicardi Hereditary and acquired C1-inhibitor deficiency: biological and chemical characteristics in 235 patients Med. (Baltimore) 71 1992 206 215
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    • Exhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angioedema
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.