WordNet
- a decrease in size of an organ caused by disease or disuse (同)wasting, wasting away
- undergo atrophy; "Muscles that are not used will atrophy"
- any weakening or degeneration (especially through lack of use) (同)withering
PrepTutorEJDIC
- (栄養不良などによる)萎縮(いしゅく) / (一般的に)衰退,退化 / 萎縮する,衰退する / …'を'萎縮させる,衰退させる
UpToDate Contents
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- 1. 脊髄小脳変性症 the spinocerebellar ataxias
- 2. 舞踏病の概要 overview of chorea
- 3. 症候性（二次性）ミオクローヌス symptomatic secondary myoclonus
- 4. ハンチントン病：臨床的特徴および診断 huntington disease clinical features and diagnosis
- 5. 遺伝性運動失調の概要 overview of the hereditary ataxias
English Journal
- Amelioration of disabling myoclonus in a case of DRPLA by levetiracetam.
- Kobayashi K, Takeuchi A, Oka M, Akiyama M, Ohtsuka Y.SourceDepartment of Child Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences and Okayama University Hospital, Okayama, Japan.
- Brain & development.Brain Dev.2011 Aug 31. [Epub ahead of print]
- We report on an 18-year-old male patient with dentatorubral-pallidoluysian atrophy (DRPLA) (number of CAG repeats: 68) with progressive myoclonus epilepsy (PME), who showed a dramatic response to levetiracetam in terms of the intensity of myoclonus. He began to have convulsive seizures and myoclonus
- PMID 21889282
- FAT10 protein binds to polyglutamine proteins and modulates their solubility.
- Nagashima Y, Kowa H, Tsuji S, Iwata A.SourceDepartment of Molecular Neuroscience on Neurodegeneration, University of Tokyo, Tokyo, Japan.
- The Journal of biological chemistry.J Biol Chem.2011 Aug 26;286(34):29594-600. Epub 2011 Jul 8.
- Expansion of polyglutamine (pQ) chain by expanded CAG repeat causes dominantly inherited neurodegeneration such as Huntington disease, dentatorubral-pallidoluysian atrophy (DRPLA), and numbers of other spinocerebellar ataxias. Expanded pQ disrupts the stability of the pQ-harboring protein and increa
- PMID 21757738
Japanese Journal
- 脳変性疾患におけるCT/MRI--スクリーニングとして知っておくべきこと (脳疾患画像読影のコツとpitfall)
- 高橋 哲哉,西澤 正豊
- Monthly book medical rehabilitation (132), 160-168, 2011-06
- NAID 40018889154
- 長期経過観察をした歯状核赤核淡蒼球ルイ体萎縮症(DRPLA)の28歳女性 : 歩行分析の有用性
- 栗原 まな,高橋 佳代子,小萩沢 利孝,山内 裕子,井田 博幸
- 脳と発達 41(4), 294-298, 2009-07-01
- NAID 10024846428
Related Links
- Dentatorubral-pallidoluysian atrophy (DRPLA) is an autosomal dominant spinocerebellar degeneration caused by an expansion of a CAG repeat encoding a polyglutamine tract in the atrophin-1 protein. It is also known as Haw River ...
Related Pictures
★リンクテーブル★
| リンク元 | 「淡蒼球ルイ体萎縮」「淡蒼球ルイ体萎縮症」 |
| 拡張検索 | 「dentatorubral-pallidoluysian atrophy」「dentatorubral-pallidoluysian atrophy gene」「dentatorubropallidoluysian atrophy」 |
| 関連記事 | 「atrophy」 |
「淡蒼球ルイ体萎縮」
「淡蒼球ルイ体萎縮症」
「dentatorubral-pallidoluysian atrophy」
「dentatorubral-pallidoluysian atrophy gene」
「dentatorubropallidoluysian atrophy」
「atrophy」
- n.