Hereditary Angioedema Presenting with Recurrent Ascites
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology,Physiology
Link
http://link.springer.com/content/pdf/10.1007/s10620-005-1272-2.pdf
Reference15 articles.
1. 1. Donaldson VH, Evans RR: A biochemial abnormality in hereditary angioneurotic edema: Absence of serum inhibitor of C1-esterase. Am J Med 35:37?44, 1963
2. 2. Donaldson VH: Hereditary angioneurotic edema. Dis Mon 26:1?37, 1979
3. 3. Agostini A, Cicardi M: Hereditary and acquired C1-inhibitor deficiency: Biological and clinical characteristics in 235 patients. Medicine 71:206?215, 1992
4. 4. Stoppa-Lyonnet D, Tosi M, Laurent J: Altered C1 inhibitor genes in type I hereditary angioedema. N Engl J Med 317:1?6, 1987
5. 5. Rosen FS, Chharache P, Pensky J: Hereditary angioneurotic edema: Two genetic variants. Science 148:957?958, 1965
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1. Hereditary Angioedema: a Challenging Diagnosis for the Gastroenterologist;Journal of Interdisciplinary Medicine;2016-12-01
2. Erratum to: Hereditary Angioedema Presenting with Recurrent Ascites;Digestive Diseases and Sciences;2016-11-14
3. Successful use of daily intravenous infusion of C1 esterase inhibitor concentrate in the treatment of a hereditary angioedema patient with ascites, hypovolemic shock, sepsis, renal and respiratory failure;Allergy, Asthma & Clinical Immunology;2014-12
4. Œdème angioneurotique héréditaire compliqué d’invagination colocolique;Archives de Pédiatrie;2008-03
5. Gastrointestinal Involvement in a Case of Hereditary Angioedema: Could the Early Weaning Have Had a Role?;The American Journal of the Medical Sciences;2007-09
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