The relationship between complement levels and disease activity in Japanese family cases of hereditary angioedema with C1-INH deficiency-Reference-Cited by-同舟云学术

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

Published:2018-10 Issue:4 Volume:67 Page:518-520
ISSN:1323-8930
Container-title:Allergology International
language:en
Short-container-title:Allergology International

Author:

Fukunaga Atsushi,Tsuchiyama Shinji,Lee Kasumi,Washio Ken,Hashimura Chinami,Horiuchi Takahiko,Nishigori Chikako

Funder

Japan Society for the Promotion of Science KAKENHI

Ministry of Education, Culture, Sports, Science, and Technology, Japan

Publisher

Elsevier BV

Subject

General Medicine,Immunology and Allergy

Reference9 articles.

1. Hereditary and acquired C1-inhibitor deficiency: biological and clinical characteristics in 235 patients;Agostoni;Medicine (Baltim),1992

2. Hereditary angioedema in Japan: genetic analysis of 13 unrelated cases;Yamamoto;Am J Med Sci,2012

3. Novel and recurrent C1 inhibitor gene mutations in nine Japanese patients with hereditary angioedema;Iwamoto;J Dermatol Sci,2012

4. International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency;Farkas;Allergy,2017

5. Parameters of the classical complement pathway predict disease severity in hereditary angioedema;Csuka;Clin Immunol,2011

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Systemic lupus erythematosus with various clinical manifestations in a patient with hereditary angioedema: a case report;Allergy, Asthma & Clinical Immunology;2022-09-18

2. Cut-off value of C1-inhibitor function for the diagnosis of hereditary angioedema due to C1-inhibitor deficiency;Intractable & Rare Diseases Research;2021-02-28

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