Mechanizmy svalového zánětu a jejich klinické projevy u nemocných polymyozitidou a dermatomyozitidou

Mechanizmy svalového zánětu a jejich klinické projevy u nemocných polymyozitidou a dermatomyozitidou

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Idiopathic inflammatory myopathies (IIM) is a heterogeneous group of acquired diseases with varying course and prognosis nehnisavým caused by inflammation of striated muscle. Clinically they are characterized primarily by proximal muscular weakness. On the basis of specific clinical, histopathologic...

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Main Author: Studýnková-Tomasová, Jana
Other Authors: Vencovský, Jiří
Format: Doctoral Thesis
Language:Czech
Published: 2006
Online Access:http://www.nusl.cz/ntk/nusl-450607
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spelling ndltd-nusl.cz-oai-invenio.nusl.cz-4506072021-09-20T05:10:13Z Mechanizmy svalového zánětu a jejich klinické projevy u nemocných polymyozitidou a dermatomyozitidou Mechanisms of muscle inflammation and clinical manifestations in patients polymyositis and dermatomyositis Studýnková-Tomasová, Jana Vencovský, Jiří Bartůňková, Jiřina Hrnčíř, Zbyněk Idiopathic inflammatory myopathies (IIM) is a heterogeneous group of acquired diseases with varying course and prognosis nehnisavým caused by inflammation of striated muscle. Clinically they are characterized primarily by proximal muscular weakness. On the basis of specific clinical, histopathological, immunological and demographic features of the breakers can be divided into three subgroups dermatomyositis (DM), polymyositis (PM) and inclusion bodies with myositis (IBM). The aetiology of these diseases is unknown and there is also rooted difficulties with their treatment. The common objective of the project was to try to map out the mechanisms leading to inflammatory infiltration of muscles, muscle tissue edema and tissue damage, and subsequently to clinical manifestations of disease in patients with PM and DM. 2006 info:eu-repo/semantics/doctoralThesis http://www.nusl.cz/ntk/nusl-450607 cze info:eu-repo/semantics/restrictedAccess
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language Czech
format Doctoral Thesis
sources NDLTD
description Idiopathic inflammatory myopathies (IIM) is a heterogeneous group of acquired diseases with varying course and prognosis nehnisavým caused by inflammation of striated muscle. Clinically they are characterized primarily by proximal muscular weakness. On the basis of specific clinical, histopathological, immunological and demographic features of the breakers can be divided into three subgroups dermatomyositis (DM), polymyositis (PM) and inclusion bodies with myositis (IBM). The aetiology of these diseases is unknown and there is also rooted difficulties with their treatment. The common objective of the project was to try to map out the mechanisms leading to inflammatory infiltration of muscles, muscle tissue edema and tissue damage, and subsequently to clinical manifestations of disease in patients with PM and DM.
author2 Vencovský, Jiří
author_facet Vencovský, Jiří
Studýnková-Tomasová, Jana
author Studýnková-Tomasová, Jana
spellingShingle Studýnková-Tomasová, Jana
Mechanizmy svalového zánětu a jejich klinické projevy u nemocných polymyozitidou a dermatomyozitidou
author_sort Studýnková-Tomasová, Jana
title Mechanizmy svalového zánětu a jejich klinické projevy u nemocných polymyozitidou a dermatomyozitidou
title_short Mechanizmy svalového zánětu a jejich klinické projevy u nemocných polymyozitidou a dermatomyozitidou
title_full Mechanizmy svalového zánětu a jejich klinické projevy u nemocných polymyozitidou a dermatomyozitidou
title_fullStr Mechanizmy svalového zánětu a jejich klinické projevy u nemocných polymyozitidou a dermatomyozitidou
title_full_unstemmed Mechanizmy svalového zánětu a jejich klinické projevy u nemocných polymyozitidou a dermatomyozitidou
title_sort mechanizmy svalového zánětu a jejich klinické projevy u nemocných polymyozitidou a dermatomyozitidou
publishDate 2006
url http://www.nusl.cz/ntk/nusl-450607
work_keys_str_mv AT studynkovatomasovajana mechanizmysvalovehozanetuajejichklinickeprojevyunemocnychpolymyozitidouadermatomyozitidou
AT studynkovatomasovajana mechanismsofmuscleinflammationandclinicalmanifestationsinpatientspolymyositisanddermatomyositis
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