WordNet
- (of diseases) arising from an unknown cause; "idiopathic epilepsy"
- myositis characterized by weakness of limb and neck muscles and much muscle pain and swelling; progression and severity vary among individuals
PrepTutorEJDIC
- 特発性疾患の(病気の原因があいまいな,また不明な場合)
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- 1. 成人における皮膚筋炎および多発性筋炎の診断および鑑別診断 diagnosis and differential diagnosis of dermatomyositis and polymyositis in adults
- 2. 成人における皮膚筋炎および多発性筋炎の臨床症状 clinical manifestations of dermatomyositis and polymyositis in adults
- 3. 成人における皮膚筋炎および多発性筋炎の初期治療 initial treatment of dermatomyositis and polymyositis in adults
- 4. 皮膚筋炎および多発性筋炎における間質性肺疾患：臨床症状および診断 interstitial lung disease in dermatomyositis and polymyositis clinical manifestations and diagnosis
- 5. Juvenile dermatomyositis and polymyositis: Diagnosis
English Journal
- Cardiac involvement in polymyositis and dermatomyositis.
- Danieli MG1, Gelardi C2, Guerra F3, Cardinaletti P1, Pedini V1, Gabrielli A1.
- Autoimmunity reviews.Autoimmun Rev.2016 May;15(5):462-5. doi: 10.1016/j.autrev.2016.01.015. Epub 2016 Jan 28.
- PMID 26826433
- Pediatric Mixed Connective Tissue Disease.
- Berard RA1,2, Laxer RM3,4.
- Current rheumatology reports.Curr Rheumatol Rep.2016 May;18(5):28. doi: 10.1007/s11926-016-0576-x.
- Pediatric-onset mixed connective tissue disease is among the rare disease entities in pediatric rheumatology and includes features of arthritis, polymyositis/dermatomyositis, systemic lupus erythematosus, and systemic sclerosis. Accurate recognition and diagnosis of the disease is paramount to preve
- PMID 27032791
- Epidemiologic analysis of the clinical features of Japanese patients with polymyositis and dermatomyositis.
- Tomimitsu H1, Ohta A2, Nagai M2, Nishina M2, Ishihara S3, Kohsaka H4.
- Modern rheumatology / the Japan Rheumatism Association.Mod Rheumatol.2016 May;26(3):398-402. doi: 10.3109/14397595.2015.1091137. Epub 2015 Oct 27.
- OBJECTIVES: This study aimed to investigate the clinical characteristics of polymyositis/dermatomyositis (PM/DM) in Japan by analyzing data from the nationwide registration system.METHODS: The data of the registration system in 2009 were analyzed to investigate patient numbers, sex, clinical symptom
- PMID 26375202
Japanese Journal
- 筋組織内筋束間の間質性筋炎を伴った全身性炎症性疾患の3例
- 日本小児科学会雑誌 = The journal of the Japan Pediatric Society 118(1), 23-29, 2014-01
- NAID 40019950075
- 抗SRP抗体陽性の重症多発性筋炎に免疫グロブリン大量療法(IVIG)が奏効した一例
- 臨床リウマチ 26(1), 63-68, 2014
- NAID 130005072316
- 膠原病内科医が診る筋炎 (特集 Close Encounters : 臨床神経学と臨床免疫学の遭遇と未来)
- Brain and nerve : 神経研究の進歩 65(11), 1275-1282, 2013-11
- NAID 40019860705
Related Links
- Polymyositis. Polymyositis is an idiopathic inflammatory myopathy that causes symmetrical, proximal muscle weakness; elevated skeletal muscle enzyme levels; and characteristic electromyography (EMG) and muscle ... ...
- Polymyositis is an idiopathic inflammatory myopathy that causes symmetrical, proximal muscle weakness; elevated skeletal muscle enzyme levels; and characteristic electromyography (EMG) and muscle biopsy findings (see the ...
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★リンクテーブル★
| リンク元 | 「特発性多発性筋炎」 |
| 関連記事 | 「idiopathic」 |
「特発性多発性筋炎」
「idiopathic」
- adj.
- 特発の、特発性の。原因不明の。ある個人に独特の