Hereditary angioedema with dominant cerebral symptoms finally leading to chronic disability
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),General Medicine,Surgery
Reference7 articles.
1. A review of the reported defects in the human C1 esterase inhibitor gene producing hereditary angioedema including four new mutations;Bowen;Clin Immunol,2001
2. C1 inhibitor, a multi-functional serine protease inhibitor;Davis;Thromb Haemost,2010
3. Hereditary angioedema in childhood: an approach to management;Ebo;Paediatr Drugs,2010
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
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1. Neurologic and Psychiatric Manifestations of Bradykinin-Mediated Angioedema: Old and New Challenges;International Journal of Molecular Sciences;2023-07-29
2. Hereditary angio-oedema with C1 inhibitor deficiency type I, an unusual stroke mimic;BMJ Case Reports;2022-04
3. An unusual presentation of hereditary angioedema type II with amnesia, poor concentration, and headache;Annals of Allergy, Asthma & Immunology;2020-10
4. Knockdown of circulating C1 inhibitor induces neurovascular impairment, glial cell activation, neuroinflammation, and behavioral deficits;Glia;2019-03-18
5. The Diagnosis of Hereditary Angioedema: Family Caregivers’ Experiences;Clinical Nursing Research;2018-06-04
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