A novel mutation in the coagulation factor 12 gene in patients with hereditary angioedema and normal C1-inhibitor

被引：0
|
作者：
Bork, K. [1 ]
Wulff, K. [2 ]
Meinke, P. [2 ]
Wagner, N. [3 ]
Hardt, J. [4 ]
Witzke, G. [1 ]
机构：
[1] Univ Hosp Mainz, Dept Dermatol, Mainz, Germany
[2] Ernst Moritz Arndt Univ Greifswald, Inst Human Genet, Greifswald, Germany
[3] Dist Hosp Darmstadt, Dept Dermatol, Darmstadt, Germany
[4] Johannes Gutenberg Univ Mainz, Dept Med Psychol & Med Sociol, D-55122 Mainz, Germany
来源：
ALLERGY | 2011年 / 66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：
1115
引用
收藏
页码：429 / 429
页数：1
相关论文
共 50 条
  • [21] Cinryze™ (C1-inhibitor) for the treatment of hereditary angioedema
    Gompels, Mark M.
    Lock, Robert John
    EXPERT REVIEW OF CLINICAL IMMUNOLOGY, 2011, 7 (05) : 569 - 573
  • [22] C1-INHIBITOR CONCENTRATE FOR TREATMENT OF HEREDITARY ANGIOEDEMA
    PHILLIPS, M
    NEW ENGLAND JOURNAL OF MEDICINE, 1980, 303 (09): : 526 - 527
  • [23] Glucocorticoid receptor gene polymorphisms in hereditary angioedema with C1-inhibitor deficiency
    Zotter, Zsuzsanna
    Nagy, Zsolt
    Patocs, Attila
    Csuka, Dorottya
    Veszeli, Nora
    Kohalmi, Kinga Viktoria
    Farkas, Henriette
    ORPHANET JOURNAL OF RARE DISEASES, 2017, 12
  • [24] Glucocorticoid receptor gene polymorphisms in hereditary angioedema with C1-inhibitor deficiency
    Zsuzsanna Zotter
    Zsolt Nagy
    Attila Patócs
    Dorottya Csuka
    Nóra Veszeli
    Kinga Viktória Kőhalmi
    Henriette Farkas
    Orphanet Journal of Rare Diseases, 12
  • [25] Hereditary Angioedema-Associated Acute Pancreatitis in C1-Inhibitor Deficient and Normal C1-Inhibitor Patients: Case Reports and Literature Review
    Veronez, Camila Lopes
    Campos, Regis Albuquerque
    Constantino-Silva, Rosemeire Navickas
    Nicolicht, Priscila
    Pesquero, Joao Bosco
    Grumach, Anete Sevciovic
    FRONTIERS IN MEDICINE, 2019, 6
  • [26] Oestrogen dependent hereditary angioedema with normal C1 inhibitor caused by a mutation in coagulation factor XII in a Spanish family
    Gomez-Traseira, C.
    Lopez-Lera, A.
    Caballero, T.
    Prior, N.
    Drouet, C.
    Lopez-Trascasa, M.
    ALLERGY, 2009, 64 : 283 - 283
  • [27] Hereditary angioedema in a Jordanian family with a novel missense mutation in the C1-inhibitor N-terminal domain
    Jaradat, Saied A.
    Caccia, Sonia
    Rawashdeh, Rifaat
    Melhem, Motasem
    Al-Hawamdeh, Ali
    Carzaniga, Thomas
    Haddad, Hazem
    MOLECULAR IMMUNOLOGY, 2016, 71 : 123 - 130
  • [28] Hereditary angioedema with normal C1Inhibitor and factor XII mutation: a French cohort
    Boccon-Gibod, I
    Bouillet, L.
    Gompel, A.
    Fain, O.
    Du-Thanh, A.
    Raison-Peyron, N.
    Ollivier, Y.
    Gayet, S.
    Pralong, P.
    Djenouhat, K.
    Kirk, R.
    ALLERGY, 2013, 68 : 432 - 432
  • [29] Recombinant human C1-inhibitor for the treatment of acute angioedema attacks in patients with hereditary angioedema
    Zuraw, Bruce
    Cicardi, Marco
    Levy, Robyn J.
    Nuijens, Jan H.
    Relan, Anurag
    Visscher, Sonja
    Haase, Gerald
    Kaufman, Leonard
    Hack, C. Erik
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2010, 126 (04) : 821 - U229
  • [30] 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
12345