Hereditary Angioedema with Normal C1-INH with Versus without a Specific Mutation in the F12 Gene

被引：0
|
作者：
Bork, Konrad [1 ]
Wulff, Karin [2 ]
Witzke, Guenther [1 ]
Hardt, Jochen [3 ]
机构：
[1] Johannes Gutenberg Univ Mainz, Dept Dermatol, D-55122 Mainz, Germany
[2] Ernst Moritz Arndt Univ Greifswald, Univ Med, Greifswald, Germany
[3] Johannes Gutenberg Univ Mainz, Dept Med Psychol & Med Sociol, D-55122 Mainz, Germany
来源：
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY | 2015年 / 135卷 / 02期
关键词：
D O I：
10.1016/j.jaci.2014.12.1582
中图分类号：
R392 [医学免疫学];
学科分类号：
100102 ;
摘要：
641
引用
收藏
页码：AB198 / AB198
页数：1
相关论文
共 50 条
  • [1] Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutations
    Bork, K.
    Wulff, K.
    Witzke, G.
    Hardt, J.
    ALLERGY, 2015, 70 (08) : 1004 - 1012
  • [2] Tamoxifen, a Trigger Factor of Hereditary Angioedema with Normal C1-INH with a Specific Mutation in the F12 Gene (HAE-FXII)
    Rietz, Stephan
    Bork, Konrad
    Wulff, Karin
    Witzke, Guenther
    Hardt, Jochen
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2016, 137 (02) : AB254 - AB254
  • [3] Treatment for hereditary angioedema with normal C1-INH and specific mutations in the F12 gene (HAE-FXII)
    Bork, K.
    Wulff, K.
    Witzke, G.
    Hardt, J.
    ALLERGY, 2017, 72 (02) : 320 - 324
  • [4] Screening of p.Lys330Glu (K330E) mutation in the plasminogen gene in hereditary angioedema patients with normal C1-INH and without mutation in the F12 gene
    Birben, E.
    Karakaya, G.
    Sahiner, U.
    Celebioglu, E.
    Kalyoncu, A. F.
    Sekerel, B. E.
    Soyer, O. U.
    ALLERGY, 2018, 73 : 284 - 284
  • [5] C1-INH concentrate for prophylaxis during pregnancy in hereditary angioedema with normal C1-INH
    Valencia, Reimus M.
    Wu, Shan Shan
    Gibbons, Kathleen R.
    Peppers, Brian P.
    Hostoffer, Robert W.
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2019, 7 (02): : 754 - 754
  • [6] Pregnancies in hereditary angioedema with normal C1 inhibitor with or without F12 gene mutations
    Bork, K.
    Witzke, G.
    Wulff, K.
    Hardt, J.
    ALLERGY, 2015, 70 : 59 - 59
  • [7] Estrogens and F12 gene mutations in women with antihistamine-resistant angioedema with normal C1-INH and negative family history
    Bork, K.
    Wulff, K.
    Witzke, G.
    Stanger, C.
    Lohse, P.
    Hardt, J.
    ALLERGY, 2014, 69 : 87 - 87
  • [8] Treatment with icatibant in hereditary angioedema with normal C1 inhibitor without F12 gene mutations
    Bork, K.
    Wulff, K.
    Hardt, J.
    ALLERGY, 2015, 70 : 472 - 473
  • [9] Hereditary Angioedema with Normal C1-INH (HAE Type III)
    Riedl, Marc A.
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2013, 1 (05): : 427 - 432
  • [10] Clinical features of a Brazilian family with hereditary angioedema with normal C1 inhibitor and mutation in F12 gene
    Ferriani, M. P. L.
    Maia, L.
    Nociti, T. M.
    Dias, M. M.
    Moreno, A. S.
    Arruda, L. K.
    ALLERGY, 2016, 71 : 555 - 556
12345