Deficiencies of C1 inhibitor
Author:
Publisher
Elsevier BV
Subject
Gastroenterology
Reference47 articles.
1. A biochemical abnormality in hereditary angioneurotic edema: absence of serum inhibitor of C′1-esterase;Donaldson;Am J Med,1963
2. Acquired C1 deficiency in lymphosarcoma;Caldwell;Clin Immunol Immunopathol,1972
3. Hereditary angioneurotic edema. A clinical survey;Donaldson;Pediatrics,1966
4. Action of complement in hereditary angioneurotic edema: the role of C′1-esterase;Donaldson;J Clin Invest,1964
5. The metabolism of C1 inhibitor and C1q in patients with acquired C1-inhibitor deficiency;Melamed;J Allergy Clin Immunol,1986
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1. Mutational spectrum and genotype-phenotype relationships in a cohort of Romanian hereditary angioedema patients caused by C1 inhibitor deficiency;Revista Romana de Medicina de Laborator;2019-07-01
2. Complement: Measurement;eLS;2015-09-14
3. High-molecular-weight kininogen cleavage correlates with disease states in the bradykinin-mediated angioedema due to hereditary C1-inhibitor deficiency;Clinical & Experimental Allergy;2014-11-24
4. Hereditary angioedema with C1 inhibitor deficiency: clinical presentation and quality of life of 193 French patients;Annals of Allergy, Asthma & Immunology;2013-10
5. Potentiation of C1-esterase inhibitor by heparin and interactions with C1s protease as assessed by surface plasmon resonance;Biochimica et Biophysica Acta (BBA) - General Subjects;2012-01
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