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Volumn 114, Issue 2, 2015, Pages 154-156

Idiopathic angioedema with F12 mutation: Is it a new entity'

Author keywords

[No Author keywords available]

Indexed keywords

ANTIHISTAMINIC AGENT; BRADYKININ; COMPLEMENT COMPONENT C1Q; COMPLEMENT COMPONENT C4; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; NONSTEROID ANTIINFLAMMATORY AGENT; PROLINE; PROLINE RICH PROTEIN; TRANEXAMIC ACID; BLOOD CLOTTING FACTOR 12; COMPLEMENT COMPONENT C1S INHIBITOR;

EID: 84921597282     PISSN: 10811206     EISSN: 15344436     Source Type: Journal    
DOI: 10.1016/j.anai.2014.11.018     Document Type: Article
Times cited : (9)

References (9)
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  • 2
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    • Hereditary angioedema with normal C1 inhibitor function: Consensus of an international expert panel
    • B.L. Zuraw, K. Bork, and K.E. Binkley Hereditary angioedema with normal C1 inhibitor function: consensus of an international expert panel Allergy Asthma Proc 33 suppl 1 2012 S145 S156
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    • Zuraw, B.L.1    Bork, K.2    Binkley, K.E.3
  • 3
    • 33646026697 scopus 로고    scopus 로고
    • Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor
    • G. Dewald, and K. Bork Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor Biochem Biophys Res Commun 343 2006 1286 1289
    • (2006) Biochem Biophys Res Commun , vol.343 , pp. 1286-1289
    • Dewald, G.1    Bork, K.2
  • 4
    • 80053130267 scopus 로고    scopus 로고
    • A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor
    • K. Bork, K. Wulff, P. Meinke, N. Wagner, J. Hardt, and G. Witzke A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor Clin Immunol 141 2011 31 35
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    • Bork, K.1    Wulff, K.2    Meinke, P.3    Wagner, N.4    Hardt, J.5    Witzke, G.6
  • 5
    • 84884374545 scopus 로고    scopus 로고
    • Novel duplication in the F12 gene in a patient with recurrent angioedema
    • N. Kiss, E. Barabas, and K. Varnai Novel duplication in the F12 gene in a patient with recurrent angioedema Clin Immunol 149 2012 142 145
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    • Kiss, N.1    Barabas, E.2    Varnai, K.3
  • 6
    • 79952507041 scopus 로고    scopus 로고
    • Factor XII Osaka: Abnormal factor XII with partially defective prekallikrein cleavage activity
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    • (2011) Thromb Haemost , vol.105 , pp. 473-478
    • Iijima, K.1    Arakawa, Y.2    Sugahara, Y.3
  • 7
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    • The novel acceptor splice site mutation 11396(G→A) in the factor XII gene causes a truncated transcript in cross-reacting material negative patients
    • M. Schloesser, S. Hofferbert, U. Bartz, G. Lutze, B. Lämmle, and W. Engel The novel acceptor splice site mutation 11396(G→A) in the factor XII gene causes a truncated transcript in cross-reacting material negative patients Hum Mol Genet 4 1995 1235 1237
    • (1995) Hum Mol Genet , vol.4 , pp. 1235-1237
    • Schloesser, M.1    Hofferbert, S.2    Bartz, U.3    Lutze, G.4    Lämmle, B.5    Engel, W.6
  • 8
    • 80055104672 scopus 로고    scopus 로고
    • Factor XII gene mutation in the Hageman family
    • Y.O. Xu-Cai, J. Shen, and S. Chen Factor XII gene mutation in the Hageman family J Thromb Haemost 9 2011 2329 2331
    • (2011) J Thromb Haemost , vol.9 , pp. 2329-2331
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  • 9
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    • Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.