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Lessons learned from an animal model of Kawasaki disease
Kawasaki disease is the most common cause of multisystem vasculitis in childhood. Kawasaki disease has been reported throughout the world and affects children of all ethnicity. Coronary artery damage from Kawasaki disease is the leading cause of acquired heart disease in children in the developed wo...
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Published in: | Clinical and experimental rheumatology 2007, Vol.25 (1), p.S69-S71 |
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container_title | Clinical and experimental rheumatology |
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creator | YEUNG, R. S. M |
description | Kawasaki disease is the most common cause of multisystem vasculitis in childhood. Kawasaki disease has been reported throughout the world and affects children of all ethnicity. Coronary artery damage from Kawasaki disease is the leading cause of acquired heart disease in children in the developed world. Diagnostic tests and prognostic markers are lacking, and questions remain unanswered in our understanding of the etiopathogenesis of the disease, thus limiting our ability to improve therapy and coronary outcome. In this article I will review advances made in an animal model of disease, which has helped advance our understanding of the etiology and pathogenesis of this fascinating clinical syndrome. |
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S. M</creator><creatorcontrib>YEUNG, R. S. M</creatorcontrib><description>Kawasaki disease is the most common cause of multisystem vasculitis in childhood. Kawasaki disease has been reported throughout the world and affects children of all ethnicity. Coronary artery damage from Kawasaki disease is the leading cause of acquired heart disease in children in the developed world. Diagnostic tests and prognostic markers are lacking, and questions remain unanswered in our understanding of the etiopathogenesis of the disease, thus limiting our ability to improve therapy and coronary outcome. In this article I will review advances made in an animal model of disease, which has helped advance our understanding of the etiology and pathogenesis of this fascinating clinical syndrome.</description><identifier>ISSN: 0392-856X</identifier><identifier>EISSN: 1593-098X</identifier><identifier>PMID: 17428374</identifier><language>eng</language><publisher>Pisa: Clinical and Experimental Rheumatology</publisher><subject>Animals ; Biological and medical sciences ; Child ; Coronary Aneurysm - diagnosis ; Coronary Aneurysm - prevention & control ; Disease Models, Animal ; Humans ; Immunoglobulins, Intravenous - therapeutic use ; Medical sciences ; Mice ; Mice, Inbred Strains ; Mucocutaneous Lymph Node Syndrome - drug therapy ; Mucocutaneous Lymph Node Syndrome - etiology ; Mucocutaneous Lymph Node Syndrome - pathology ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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M</creatorcontrib><title>Lessons learned from an animal model of Kawasaki disease</title><title>Clinical and experimental rheumatology</title><addtitle>Clin Exp Rheumatol</addtitle><description>Kawasaki disease is the most common cause of multisystem vasculitis in childhood. Kawasaki disease has been reported throughout the world and affects children of all ethnicity. Coronary artery damage from Kawasaki disease is the leading cause of acquired heart disease in children in the developed world. Diagnostic tests and prognostic markers are lacking, and questions remain unanswered in our understanding of the etiopathogenesis of the disease, thus limiting our ability to improve therapy and coronary outcome. In this article I will review advances made in an animal model of disease, which has helped advance our understanding of the etiology and pathogenesis of this fascinating clinical syndrome.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Coronary Aneurysm - diagnosis</subject><subject>Coronary Aneurysm - prevention & control</subject><subject>Disease Models, Animal</subject><subject>Humans</subject><subject>Immunoglobulins, Intravenous - therapeutic use</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Mucocutaneous Lymph Node Syndrome - drug therapy</subject><subject>Mucocutaneous Lymph Node Syndrome - etiology</subject><subject>Mucocutaneous Lymph Node Syndrome - pathology</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p239t-4a18ae8449293e7005b7a06a865404ff50a0e0e7ab6cfeecda35e0d4f20374d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Coronary Aneurysm - diagnosis</topic><topic>Coronary Aneurysm - prevention & control</topic><topic>Disease Models, Animal</topic><topic>Humans</topic><topic>Immunoglobulins, Intravenous - therapeutic use</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Mucocutaneous Lymph Node Syndrome - drug therapy</topic><topic>Mucocutaneous Lymph Node Syndrome - etiology</topic><topic>Mucocutaneous Lymph Node Syndrome - pathology</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lessons learned from an animal model of Kawasaki disease</atitle><jtitle>Clinical and experimental rheumatology</jtitle><addtitle>Clin Exp Rheumatol</addtitle><date>2007</date><risdate>2007</risdate><volume>25</volume><issue>1</issue><spage>S69</spage><epage>S71</epage><pages>S69-S71</pages><issn>0392-856X</issn><eissn>1593-098X</eissn><abstract>Kawasaki disease is the most common cause of multisystem vasculitis in childhood. Kawasaki disease has been reported throughout the world and affects children of all ethnicity. Coronary artery damage from Kawasaki disease is the leading cause of acquired heart disease in children in the developed world. Diagnostic tests and prognostic markers are lacking, and questions remain unanswered in our understanding of the etiopathogenesis of the disease, thus limiting our ability to improve therapy and coronary outcome. In this article I will review advances made in an animal model of disease, which has helped advance our understanding of the etiology and pathogenesis of this fascinating clinical syndrome.</abstract><cop>Pisa</cop><pub>Clinical and Experimental Rheumatology</pub><pmid>17428374</pmid></addata></record> |
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language | eng |
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source | Freely Accessible Science Journals |
subjects | Animals Biological and medical sciences Child Coronary Aneurysm - diagnosis Coronary Aneurysm - prevention & control Disease Models, Animal Humans Immunoglobulins, Intravenous - therapeutic use Medical sciences Mice Mice, Inbred Strains Mucocutaneous Lymph Node Syndrome - drug therapy Mucocutaneous Lymph Node Syndrome - etiology Mucocutaneous Lymph Node Syndrome - pathology Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis |
title | Lessons learned from an animal model of Kawasaki disease |
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