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Volumn 111, Issue 1, 2013, Pages 65-66

The nebulous diagnosis of type III hereditary angioedema

Author keywords

[No Author keywords available]

Indexed keywords

BRADYKININ; COMPLEMENT COMPONENT C1S INHIBITOR;

EID: 84879551832     PISSN: 10811206     EISSN: 15344436     Source Type: Journal    
DOI: 10.1016/j.anai.2013.04.006     Document Type: Article
Times cited : (3)

References (7)
  • 1
    • 84865510557 scopus 로고    scopus 로고
    • Type III hereditary angioedema: Clinical, biochemical, and genetic characterization in thirteen northwest Spanish families
    • C. Marcos, A.L. Lera, and S. Varela Type III hereditary angioedema: clinical, biochemical, and genetic characterization in thirteen northwest Spanish families Ann Allergy Asthma Immunol 109 2012 195 200
    • (2012) Ann Allergy Asthma Immunol , vol.109 , pp. 195-200
    • Marcos, C.1    Lera, A.L.2    Varela, S.3
  • 2
    • 84865451142 scopus 로고    scopus 로고
    • Type III hereditary angioedema: Defined, but not understood
    • A. Kaplan Type III hereditary angioedema: defined, but not understood Ann Allergy Asthma Immunol 109 2012 153 154
    • (2012) Ann Allergy Asthma Immunol , vol.109 , pp. 153-154
    • Kaplan, A.1
  • 3
    • 84867674317 scopus 로고    scopus 로고
    • Images in clinical medicine: Disfiguring angioedema
    • D.G. Ebo, and C.H. Bridts Images in clinical medicine: disfiguring angioedema N Engl J Med 367 2012 1539
    • (2012) N Engl J Med , vol.367 , pp. 1539
    • Ebo, D.G.1    Bridts, C.H.2
  • 4
    • 73249128396 scopus 로고    scopus 로고
    • Pathogenesis and laboratory diagnosis of hereditary angioedema
    • B.L. Zuraw, and S.C. Christiansen Pathogenesis and laboratory diagnosis of hereditary angioedema Allergy Asthma Proc 30 2009 487 492
    • (2009) Allergy Asthma Proc , vol.30 , pp. 487-492
    • Zuraw, B.L.1    Christiansen, S.C.2
  • 5
    • 67649224409 scopus 로고    scopus 로고
    • Kallikrein-kinin system and fibrinolysis in hereditary angioedema due to factor XII gene mutation Thr309Lys
    • K. Bork, R. Kleist, and J. Hardt Kallikrein-kinin system and fibrinolysis in hereditary angioedema due to factor XII gene mutation Thr309Lys Blood Coagul Fibrinolysis 20 2009 325 332
    • (2009) Blood Coagul Fibrinolysis , vol.20 , pp. 325-332
    • Bork, K.1    Kleist, R.2    Hardt, J.3
  • 6
    • 0019129748 scopus 로고
    • Rapid fibrinolysis, augmented Hageman factor (factor XII) titers, and decreased C1 esterase inhibitor titers in women taking oral contraceptives
    • E.M. Gordon, O.D. Ratnoff, and H. Saito Rapid fibrinolysis, augmented Hageman factor (factor XII) titers, and decreased C1 esterase inhibitor titers in women taking oral contraceptives J Lab Clin Med 96 1980 762 769
    • (1980) J Lab Clin Med , vol.96 , pp. 762-769
    • Gordon, E.M.1    Ratnoff, O.D.2    Saito, H.3
  • 7
    • 80053361954 scopus 로고    scopus 로고
    • Factor XII mutations, estrogen-dependent inherited angioedema, and related conditions
    • K. Binkley Factor XII mutations, estrogen-dependent inherited angioedema, and related conditions Allergy Asthma Clin Immunol 6 2010 16
    • (2010) Allergy Asthma Clin Immunol , vol.6 , pp. 16
    • Binkley, K.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.