脊髄小脳失調症5型
- 関
- dominantly-inherited spinocerebellar ataxia、spinocerebellar ataxia、spinocerebellar ataxia type 1、spinocerebellar ataxia type 2、spinocerebellar ataxia type 4、spinocerebellar ataxia type 6、spinocerebellar ataxia type 7、spinocerebellar atrophy
WordNet
- write by means of a keyboard with types; "type the acceptance letter, please" (同)typewrite
- a small metal block bearing a raised character on one end; produces a printed character when inked and pressed on paper; "he dropped a case of type, so they made him pick them up"
- (biology) the taxonomic group whose characteristics are used to define the next higher taxon
- a subdivision of a particular kind of thing; "what type of sculpture do you prefer?"
- all of the tokens of the same symbol; "the word `element contains five different types of character"
- printed characters; "small type is hard to read"
- identify as belonging to a certain type; "Such people can practically be typed" (同)typecast
- inability to coordinate voluntary muscle movements; unsteady movements and staggering gait (同)ataxy, dyssynergia, motor_ataxia
- writing done with a typewriter (同)typewriting
PrepTutorEJDIC
- 〈C〉(…の)『型』,タイプ,類型,種類(kind)《+of+名》 / 〈C〉(その種類の特質を最もよく表している)『典型』,手本,模範《+of+名》 / 〈U〉《集合的に》活字;〈C〉(1個の)活字 / 〈U〉(印刷された)字体,活字 / 〈C〉(貨幣・メダルなどの)模様,図柄 / 〈C〉血液型(blood group) / …‘を'タイプに打つ / (…として)…‘を'分類する《+名+as+名(doing)》 / …‘の'型を決める / タイプライターを打つ
UpToDate Contents
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- 1. 脊髄小脳変性症 the spinocerebellar ataxias
- 2. 遺伝性運動失調の概要 overview of the hereditary ataxias
- 3. 舞踏病の概要 overview of chorea
- 4. 遺伝性疾患に伴う神経障害 neuropathies associated with hereditary disorders
- 5. 片麻痺性片頭痛 hemiplegic migraine
English Journal
- Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia.
- Nibbeling EAR1, Duarri A1, Verschuuren-Bemelmans CC1, Fokkens MR1, Karjalainen JM1, Smeets CJLM1, de Boer-Bergsma JJ1, van der Vries G1, Dooijes D2, Bampi GB1, van Diemen C1, Brunt E3, Ippel E2, Kremer B3, Vlak M4, Adir N5, Wijmenga C1, van de Warrenburg BPC6, Franke L1, Sinke RJ1, Verbeek DS1.
- Brain : a journal of neurology.Brain.2017 Nov 1;140(11):2860-2878. doi: 10.1093/brain/awx251.
- PMID 29053796
- β-III-spectrin spinocerebellar ataxia type 5 mutation reveals a dominant cytoskeletal mechanism that underlies dendritic arborization.
- Avery AW1, Thomas DD2, Hays TS3.
- Proceedings of the National Academy of Sciences of the United States of America.Proc Natl Acad Sci U S A.2017 Oct 31;114(44):E9376-E9385. doi: 10.1073/pnas.1707108114. Epub 2017 Oct 16.
- PMID 29078305
- Dystonia and ataxia progression in spinocerebellar ataxias.
- Kuo PH1, Gan SR2, Wang J3, Lo RY4, Figueroa KP5, Tomishon D6, Pulst SM5, Perlman S7, Wilmot G8, Gomez CM9, Schmahmann JD10, Paulson H11, Shakkottai VG11, Ying SH12, Zesiewicz T13, Bushara K14, Geschwind MD15, Xia G16, Subramony SH17, Ashizawa T18, Kuo SH19.
- Parkinsonism & related disorders.Parkinsonism Relat Disord.2017 Oct 23. pii: S1353-8020(17)30376-0. doi: 10.1016/j.parkreldis.2017.10.007. [Epub ahead of print]
- PMID 29089256
Japanese Journal
- 運動失調はみとめずパーキンソン症状を呈したspinocerebellar ataxia type 6（SCA6）の1例
- 竹島 愼一,竹田 育子,小畠 敬太郎,山下 徹,阿部 康二,栗山 勝
- 臨床神経学 55(4), 243-247, 2015
- … MSA-C）と進行性核上性麻痺の臨床診断であった．患者，母親，母親の兄（MSA-C）3名の遺伝子検査でspinocerebellar ataxia type 6（SCA6）と診断した．小脳失調はみとめず，パーキンソン症状のSCA6は非常にまれである． …
- NAID 130005066232
- 症例報告 左右差の強い下肢ジストニアをみとめたspinocerebellar ataxia type 31 (SCA31)の1例
- 齋藤 理恵,菊野 庄太,前田 明子 [他]
- 臨床神経学 = Clinical neurology 54(8), 643-647, 2014-08
- NAID 40020180883
- Spinocerebellar ataxia type 31 (SCA31)の臨床像,画像所見 : Spinocerebellar ataxia type 6 (SCA6)との小脳外症候の比較検討
- 榊原 聡子,饗場 郁子,齋藤 由扶子 [他]
- 臨床神経学 = Clinical neurology 54(6), 473-479, 2014-06
- NAID 40020121503
Related Links
- 詳細の表示を試みましたが、サイトのオーナーによって制限されているため表示できません。
- Spinocerebellar ataxia type 5 (SCA5) was originally described in an American family of Anglo-Saxon origin descending from the grandparents of President Abraham Lincoln. The genetic locus was assigned to chromosome 11.
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脊髄小脳失調症1型、脊髄小脳変性症1型
- 関
- dominantly-inherited spinocerebellar ataxia、SCA1、spinocerebellar ataxia、spinocerebellar ataxia type 2、spinocerebellar ataxia type 4、spinocerebellar ataxia type 5、spinocerebellar ataxia type 6、spinocerebellar ataxia type 7、spinocerebellar atrophy
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脊髄小脳失調症2型
- 関
- dominantly-inherited spinocerebellar ataxia、spinocerebellar ataxia、spinocerebellar ataxia type 1、spinocerebellar ataxia type 4、spinocerebellar ataxia type 5、spinocerebellar ataxia type 6、spinocerebellar ataxia type 7、spinocerebellar atrophy
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脊髄小脳失調症4型
- 関
- dominantly-inherited spinocerebellar ataxia、spinocerebellar ataxia、spinocerebellar ataxia type 1、spinocerebellar ataxia type 2、spinocerebellar ataxia type 5、spinocerebellar ataxia type 6、spinocerebellar ataxia type 7、spinocerebellar atrophy
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脊髄小脳失調症6型
- 関
- dominantly-inherited spinocerebellar ataxia、spinocerebellar ataxia、spinocerebellar ataxia type 1、spinocerebellar ataxia type 2、spinocerebellar ataxia type 4、spinocerebellar ataxia type 5、spinocerebellar ataxia type 7、spinocerebellar atrophy
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脊髄小脳失調症7型
- 関
- dominantly-inherited spinocerebellar ataxia、spinocerebellar ataxia、spinocerebellar ataxia type 1、spinocerebellar ataxia type 2、spinocerebellar ataxia type 4、spinocerebellar ataxia type 5、spinocerebellar ataxia type 6、spinocerebellar atrophy
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- (windows)ファイル内容表示(linux -> cat])
- ex. type report_20111118.jp.htm | php a.php > report_20111118.jp.jp.jp.html
- 関
- form、mode、pattern、type specimen、typed
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脊髄小脳変性症 spinocerebellar degeneration SCD = SCA
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- 関
- form、mode、pattern、type
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