Worsening Fluid Retention in a Patient with Hereditary Angioedema and End-stage Renal Disease
Author:
Affiliation:
1. Internal Medicine II, Nihon University School of Medicine
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
http://www.jstage.jst.go.jp/article/internalmedicine/43/8/43_8_708/_pdf
Reference16 articles.
1. Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedema
2. Pathogenetic and Clinical Aspects of C1 Inhibitor Deficiency
3. Activities of the MBL-associated serine proteases (MASPs) and their regulation by natural inhibitors
4. Immune complexes in hereditary angioneurotic edema (HANE)
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1. The Gut-Kidney Axis: Putative Interconnections Between Gastrointestinal and Renal Disorders;Frontiers in Endocrinology;2018-09-19
2. Leukocytosis and high hematocrit levels during abdominal attacks of hereditary angioedema;BMC Gastroenterology;2013-08-02
3. Treatment with C1-esterase inhibitor concentrate in type I or II hereditary angioedema: A systematic literature review;Allergy and Asthma Proceedings;2013-07-22
4. A Case of Hereditary Angioedema with Laryngeal Edema Leading to Suffocation;Nihon Naika Gakkai Zasshi;2013
5. 急性腹症を呈した腸管浮腫の一例;Juntendo Medical Journal;2011
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