Treatment of patients with hereditary angioedema with normal C1 inhibitor and F12 gene mutations

被引：0
|
作者：
Bork, K. [1 ]
Witzke, G. [1 ]
Wulff, K. [2 ]
Hardt, J. [3 ]
机构：
[1] Johannes Gutenberg Univ Mainz, Dept Dermatol, D-55122 Mainz, Germany
[2] Ernst Moritz Arndt Univ Greifswald, Greifswald, Germany
[3] Johannes Gutenberg Univ Mainz, Dept Med Psychol & Med Sociol, D-55122 Mainz, Germany
来源：
ALLERGY | 2015年 / 70卷
关键词：
D O I：
暂无
中图分类号：
R392 [医学免疫学];
学科分类号：
100102 ;
摘要：
1143
引用
收藏
页码：470 / 470
页数：1
相关论文
共 50 条
  • [41] Hereditary angioedema with a normal C1 inhibitor in Japanese man
    Kamiga, Mayuna
    Hayashi, Shujiro
    Ikegami, Tetsuharu
    Tokoro, Shown
    Igawa, Ken
    JOURNAL OF DERMATOLOGY, 2024, 51 (09): : e298 - e299
  • [42] Hereditary Angioedema with Normal C1 Inhibitor: An Italian Survey
    Bafunno, Valeria
    Bova, Maria
    Zanichelli, Andrea
    Suffritti, Chiara
    Montinaro, Vincenzo
    Triggiani, Massimo
    Margaglione, Maurizio
    Cicardi, Marco
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2015, 135 (02) : AB195 - AB195
  • [43] New Mutations in SERPING1, the Gene Coding for C1 Inhibitor, in Patients with Hereditary Angioedema in Brazil
    Moreno, Adriana S.
    Delcaro, Luana
    Dias, Marina M.
    Valle, Solange R.
    Franca, Alfeu T.
    Levy, Soloni
    Roxo, Persio, Jr.
    da Silva Junior, Wilson
    Arruda, Luisa Karla P.
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2015, 135 (02) : AB196 - AB196
  • [44] C1 Inhibitor Activity and Angioedema Attacks in Patients with Hereditary Angioedema
    Kaplan, Allen P.
    Pawaskar, Dipti
    Chiao, Joseph
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2020, 8 (03): : 892 - 900
  • [45] A missense mutation of the plasminogen gene in hereditary angioedema with normal C1 inhibitor in Japan
    Yakushiji, Hiromasa
    Hashimura, Chinami
    Fukuoka, Kazuhito
    Kaji, Arito
    Miyahara, Hisaaki
    Kaname, Shinya
    Horiuchi, Takahiko
    ALLERGY, 2018, 73 (11) : 2244 - 2247
  • [46] A missense mutation of the plasminogen gene in hereditary angioedema with normal C1 inhibitor in Japan
    Horiuchi, T.
    Yakushiji, H.
    Fukuoka, K.
    Miyahara, H.
    Hashimura, C.
    ALLERGY, 2019, 74 : 214 - 214
  • [47] Characterization of a partial exon 9/intron 9 deletion in the coagulation factor XII gene (F12) detected in two Turkish families with hereditary angioedema and normal C1 inhibitor
    Bork, K.
    Wulff, K.
    Hardt, J.
    Witzke, G.
    Lohse, P.
    HAEMOPHILIA, 2014, 20 (05) : e372 - e375
  • [48] C1 inhibitor gene analysis for patients with hereditary angioedema in the United Kingdom
    Mohammadi, M.
    Longhurst, H.
    Sinnott, P.
    TISSUE ANTIGENS, 2006, 67 (06): : 456 - 457
  • [49] Missense mutations of coagulation factor XII in hereditary angioedema with normal complement C1 inhibitor
    Dewald, Georg
    Bork, Konrad
    MOLECULAR IMMUNOLOGY, 2007, 44 (1-3) : 163 - 163
  • [50] Newly Found C1 Inhibitor Gene Mutation in Hereditary Angioedema Patients
    Rui Tang and Hong-yu Zhang Department of Allergy
    ChineseMedicalSciencesJournal, 2009, 24 (04) : 252 - 252
12345