Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Idiopathic myopathy"'
Autor:
Ichiro Kobayashi
Publikováno v:
Children, Vol 11, Iss 9, p 1046 (2024)
Juvenile idiopathic inflammatory myopathy (JIIM) is a rare systemic autoimmune disease characterized by skeletal muscle weakness with or without a skin rash. Juvenile dermatomyositis (JDM) is the most common subtype of JIIM, accounting for 80% of JII
Externí odkaz:
https://doaj.org/article/e222a781f8af431eb601253183c45234
High-Dimensional Cytometry Dissects Immunological Fingerprints of Idiopathic Inflammatory Myopathies
Autor:
Christopher Nelke, Marc Pawlitzki, Christina B. Schroeter, Niklas Huntemann, Saskia Räuber, Vera Dobelmann, Corinna Preusse, Andreas Roos, Yves Allenbach, Olivier Benveniste, Heinz Wiendl, Ingrid E. Lundberg, Werner Stenzel, Sven G. Meuth, Tobias Ruck
Publikováno v:
Cells, Vol 11, Iss 20, p 3330 (2022)
Chronic inflammation of skeletal muscle is the common feature of idiopathic inflammatory myopathies (IIM). Given the rarity of the disease and potential difficulty of routinely obtaining target tissue, i.e., standardized skeletal muscle, our understa
Externí odkaz:
https://doaj.org/article/06d6225a81b143049de1692e73bb1a58
Akademický článek
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Publikováno v:
Clinical, Cosmetic and Investigational Dermatology. 13:123-126
Dermatomyositis is an idiopathic myopathy involving progressive muscle weakness with skin manifestation. Diagnosis is based upon the progressive muscle weakness, skin rashes, elevated serum muscle enzymes, muscle biopsy, and abnormal electromyogram.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f759d85890c7bccd84da3666c40d4a4
https://doi.org/10.2147/ccid.s234452
https://doi.org/10.2147/ccid.s234452
Akademický článek
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Autor:
David A. Isenberg, K. E. N. Clark
Publikováno v:
European Journal of Neurology. 25:13-23
Inflammatory idiopathic myopathies are a group of autoimmune diseases affecting predominantly the proximal skeletal muscles, with raised muscle enzymes, with or without skin involvement and extramuscular organ involvement. Autoantibodies help to char
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd358d5d159e541321dccce4c9583648
https://doi.org/10.1111/ene.13357
https://doi.org/10.1111/ene.13357
Autor:
Sonja Suntrup-Krueger, Inga Claus, Tobias Warnecke, Tobias Ruck, Sven G. Meuth, Paul Muhle, Heinz Wiendl, Marc Pawlitzki, Bendix Labeit, Rainer Dziewas
Publikováno v:
Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 9, Iss 2150, p 2150 (2020)
Journal of Clinical Medicine, Vol 9, Iss 2150, p 2150 (2020)
(1) Background: Dysphagia is a clinical hallmark and part of the current American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) diagnostic criteria for idiopathic inflammatory myopathy (IIM). However, the data on dysphagia in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ca876668ba48164c1f04a300f1a51bf
https://doi.org/10.3390/jcm9072150
https://doi.org/10.3390/jcm9072150
AIM: To conduct an epidemiological investigation of an idiopathic myopathy, known as “Go Slow” (GSM), which was initially recognised in dogs used for pig hunting. A secondary aim was to describe the hunting activities, diet and health of dogs use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b8de938e4e24feee3bf2a79a3ff7d56
Autor:
Artur da Rocha Corrêa Fernandes, Leonardo Valente de Camargo, Edmar Zanoteli, Thomas M. Link, Luca Facchetti, Julio Brandao Guimaraes, Lorenzo Nardo
Publikováno v:
AJR. American journal of roentgenology. 209(6)
The purpose of this prospective study is to assess MRI findings in patients with sporadic inclusion body myositis (IBM) and correlate them with clinical and functional parameters.This study included 12 patients with biopsy-proven sporadic IBM. All pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cafc3351613435ea8b87574e201e88b
https://pubmed.ncbi.nlm.nih.gov/28952813
https://pubmed.ncbi.nlm.nih.gov/28952813
Autor:
J. Weihrauch, N. Hunzelmann
Publikováno v:
HG Zeitschrift fur Hautkrankheiten. 77:6-12
Zusammenfassung: Die Dermatomyositis ist eine seltene idiopathische entzundliche Muskelerkrankung mit charakteristischen Hautmanifestationen und Muskelschwache. Bei circa einem Drittel der Patienten finden sich krankheitsspezifische Autoantikorper, d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e412be9f09966e398195d804bf43ed00
https://doi.org/10.1046/j.1439-0353.2002.01075.x
https://doi.org/10.1046/j.1439-0353.2002.01075.x