High prevalence of epilepsy in HAE with normal C1–INH-Reference-Cited by-同舟云学术

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High prevalence of epilepsy in HAE with normal C1–INH

Published:2020-10 Issue:4 Volume:69 Page:630-632
ISSN:1323-8930
Container-title:Allergology International
language:en
Short-container-title:Allergology International

Author:

Kuwahara Saki,Fukunaga Atsushi,Ohata Marie,Nakatani Shoko,Yokoyama Daisuke,Nakauchi Emi,Yoshioka Ai,Kinoshita Masako,Nishigori Chikako

Funder

Shire

CSL Behring

Daiichi Sankyo

Publisher

Elsevier BV

Subject

General Medicine,Immunology and Allergy

Reference16 articles.

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

2. Hereditary angioedema with normal C1 inhibitor: four types and counting;Zuraw;J Allergy Clin Immunol,2018

3. Hereditary angioedema cosegregating with a novel kininogen 1 gene mutation changing the N-terminal cleavage site of bradykinin;Bork;Allergy,2019

4. Hereditary angioedema: new findings concerning symptoms, affected organs, and course;Bork;Am J Med,2006

5. Migraine-like headache in a patient with complement 1 inhibitor deficient hereditary angioedema;Chung;J Korean Med Sci,2012

Cited by 3 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. Managing Diagnosis, Treatment, and Burden of Disease in Hereditary Angioedema Patients with Normal C1-Esterase Inhibitor;Journal of Asthma and Allergy;2023-04

2. Hereditary angioedema with normal C1 inhibitor with steroid responsiveness in a patient with psychiatric comorbidities;The Journal of Dermatology;2023-01-11

3. Hereditary Angioedema: Diagnosis, Clinical Implications, and Pathophysiology;Advances in Therapy;2023-01-07

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