Pathogenetic and Clinical Aspects of C1 Inhibitor Deficiency-Reference-Cited by-同舟云学术

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Pathogenetic and Clinical Aspects of C1 Inhibitor Deficiency

Published:1998-08 Issue:2 Volume:199 Page:366-376
ISSN:0171-2985
Container-title:Immunobiology
language:en
Short-container-title:Immunobiology

Author:

Cicardi Marco,Bergamaschini Luigi,Cugno Massimo,Beretta Andrea,Zingale Lorenza C.,Colombo Monica,Agostoni Angelo

Publisher

Elsevier BV

Subject

Hematology,Immunology,Immunology and Allergy

Reference34 articles.

1. A biochemical abnormality in hereditary angioneurotic edema: absence of serum inhibitor of C1 esterase;Donaldson;Am. J. Med.,1963

2. Human C1 inhibitor primary structure, cDNA cloning, and chromosomal localization;Bock;Biochemistry,1986

3. C1 inhibitor hinge region mutations produce dysfunction by different mechanisms;Davis;Nature Genetics,1992

4. Crucial residues in the carboxy-terminal end of C1 inhibitor revealed by pathogenic mutants impaired in secretion and function;Verpy;J. Clin. Invest.,1995

5. COOH-terminal substitutions in the serpin C1 inhibitor that cause loop overinsertion and subsequent multimerization;Eldering;J. Biol. Chem.,1995

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1. Longitudinal experience with treatment of acquired angioedema using tranexamic acid;Allergy and Asthma Proceedings;2022-09-01

2. Angioedema Due to Acquired Deficiency of C1-Inhibitor: A Cohort Study in Spain and a Comparison with Other Series;The Journal of Allergy and Clinical Immunology: In Practice;2021-11

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