scholarly journals 241 The relationship between complement levels and disease activity in Japanese cases with hereditary angioedema with C1-inhibitor (C1INH) gene mutation

2017 ◽  
Vol 137 (5) ◽  
pp. S41
Author(s):  
A. Fukunaga ◽  
S. Tsuchiyama ◽  
K. Ri ◽  
C. Nishigori ◽  
T. Horiuchi
Keyword(s):  
Disease Activity ◽  
Gene Mutation ◽  
Hereditary Angioedema ◽  
C1 Inhibitor ◽  
The Relationship

scholarly journals The relationship between complement levels and disease activity in Japanese family cases of hereditary angioedema with C1-INH deficiency

2018 ◽  
Vol 67 (4) ◽  
pp. 518-520
Author(s):  
Atsushi Fukunaga ◽  
Shinji Tsuchiyama ◽  
Kasumi Lee ◽  
Ken Washio ◽  
Chinami Hashimura ◽  
...  
Keyword(s):  
Disease Activity ◽  
Hereditary Angioedema ◽  
Japanese Family ◽  
The Relationship

Plasminogen gene mutation with normal C1 inhibitor hereditary angioedema: Three additional French families

Allergy ◽  
2018 ◽  
Vol 73 (11) ◽  
pp. 2237-2239 ◽  
Author(s):  
Aude Belbézier ◽  
Gaelle Hardy ◽  
Raphael Marlu ◽  
Federica Defendi ◽  
Chantal Dumestre Perard ◽  
...  
Keyword(s):  
Gene Mutation ◽  
Hereditary Angioedema ◽  
C1 Inhibitor

Hereditary Angioedema Without C1 Inhibitor Deficiency: Observation Of Patients Homozygous For FXII GENE Mutation

2014 ◽  
Vol 133 (2) ◽  
pp. AB31
Author(s):  
Christiane Stieber ◽  
Camila Veronez ◽  
Nathalia Cagini ◽  
Elisabete Cordeiro ◽  
Anete S. Grumach ◽  
...  
Keyword(s):  
Gene Mutation ◽  
Hereditary Angioedema ◽  
C1 Inhibitor ◽  
C1 Inhibitor Deficiency

scholarly journals Switch to Icatibant in a Patient Affected by Hereditary Angioedema with High Disease Activity: A Case Report

2012 ◽  
Vol 25 (1) ◽  
pp. 269-273
Author(s):  
D. Firinu ◽  
M.P. Barca ◽  
L. Serusi ◽  
M.M. Lorrai ◽  
M.M. Peralta ◽  
...  
Keyword(s):  
Case Report ◽  
Disease Activity ◽  
Hereditary Angioedema ◽  
High Disease Activity ◽  
C1 Inhibitor ◽  
Bradykinin B2 Receptor ◽  
Acute Attacks ◽  
The Eu

Icatibant, an antagonist of the bradykinin B2 receptor, was approved for the treatment of acute attacks of hereditary angioedema in the EU in 2008. This paper presents the case of a 65-year-old woman affected by frequent acute attacks of hereditary angioedema who benefitted from a change of therapy to icatibant, following years of treatment with C1-inhibitor.

scholarly journals Coagulation Factor XII Gene Mutation in Brazilian Families with Hereditary Angioedema with Normal C1 Inhibitor

2015 ◽  
Vol 166 (2) ◽  
pp. 114-120 ◽  
Author(s):  
Adriana S. Moreno ◽  
Solange O.R. Valle ◽  
Soloni Levy ◽  
Alfeu T. França ◽  
Faradiba S. Serpa ◽  
...  
Keyword(s):  
Gene Mutation ◽  
Hereditary Angioedema ◽  
Coagulation Factor ◽  
Factor Xii ◽  
C1 Inhibitor
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