- 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
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. 全身疾患と関連した遺伝性ニューロパチー hereditary neuropathies associated with generalized disorders
- 5. 片麻痺性片頭痛 hemiplegic migraine
English Journal
- From Normal Gait to Loss of Ambulation in 6 Months: a Novel Presentation of SCA17.
- Mehanna R, Itin I.SourceCenter for Neurological Restoration, Cleveland Clinic Foundation, 9500 Euclid Avenue/U20, Cleveland, OH, 44195, USA, doc_raja_mehanna@yahoo.com.
- Cerebellum (London, England).Cerebellum.2013 Aug;12(4):568-71. doi: 10.1007/s12311-013-0466-y.
- Spinocerebellar ataxias are a group of rare and heterogeneous autosomal dominant disorders characterized by progressive ataxia and other features. Spinocerebellar ataxia 17 (SCA17) is one of the 32 subtypes described to date and is secondary to CAG/CAA repeat expansion in the gene coding for the TAT
- PMID 23475385
- The reciprocal cerebellar circuitry in human hereditary ataxia.
- Koeppen AH, Ramirez RL, Bjork ST, Bauer P, Feustel PJ.SourceResearch Service, Veterans Affairs Medical Center, 113 Holland Ave, Albany, NY, 12208, USA, arnulf.koeppen@med.va.gov.
- Cerebellum (London, England).Cerebellum.2013 Aug;12(4):493-503. doi: 10.1007/s12311-013-0456-0.
- Clinicoanatomic correlation in the spinocerebellar ataxias (SCA) and Friedreich's ataxia (FRDA) is difficult as these diseases differentially affect multiple sites in the central and peripheral nervous systems. A new way to study cerebellar ataxia is the systematic analysis of the "reciprocal cerebe
- PMID 23389921
- What Counts as Effective Genetic Counselling for Presymptomatic Testing in Late-Onset Disorders? A Study of the Consultand's Perspective.
- Guimarães L, Sequeiros J, Skirton H, Paneque M.SourceICBAS, Universidade do Porto, Porto, Portugal.
- Journal of genetic counseling.J Genet Couns.2013 Aug;22(4):437-47. doi: 10.1007/s10897-012-9561-3. Epub 2013 Jan 7.
- Genetic counselling must be offered in the context of presymptomatic testing (PST) for severe late-onset diseases; however, effective genetic counselling is not well defined, and measurement tools that allow a systematic evaluation of genetic practice are still not available. The aims of this qualit
- PMID 23292684
Japanese Journal
- 左右差の強い下肢ジストニアをみとめspinocerebellar ataxia type31（SCA31）と診断された77歳男性例
- 臨床神経学 55(6), 434-434, 2015
- NAID 130005083897
- 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
- 臨床神経学 55(4), 243-247, 2015
- NAID 130005066232
- 脊髄小脳失調症3型 (Machado-Joseph 病) における神経耳科学的所見
- Equilibrium Research 73(6), 512-520, 2014
- NAID 130004910890
Related Pictures
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「spinocerebellar ataxia type 1」
- 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
「spinocerebellar ataxia type 2」
- 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
「spinocerebellar ataxia type 5」
- 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
「spinocerebellar ataxia type 6」
- 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
「spinocerebellar ataxia type 7」
- 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
「type」
- n.
- (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
「spinocerebellar ataxia」
[★] 脊髄小脳変性症 spinocerebellar degeneration SCD = SCA
「typed」
- adj.
- 型の
「typing」
- n.
- タイプで打つこと、タイピング。分類