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
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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English Journal
- Saccadic latency is prolonged in Spinocerebellar Ataxia type 2 and correlates with the frontal-executive dysfunctions.
- Rodriguez-Labrada R, Velazquez-Perez L, Seigfried C, Canales-Ochoa N, Auburger G, Medrano-Montero J, Sanchez-Cruz G, Aguilera-Rodriguez R, Laffita-Mesa J, Vazquez-Mojena Y, Verdecia-Ramirez M, Motta M, Quevedo-Batista Y.SourceCentre for the Research and Rehabilitation of Hereditary Ataxias, Holguin, Cuba.
- Journal of the neurological sciences.J Neurol Sci.2011 Jul 15;306(1-2):103-7. Epub 2011 Apr 9.
- Data on saccadic latency in patients with Spinocerebellar Ataxia 2 (SCA2) are sparse and contradictory. In order to determine whether saccadic latency is definitely prolonged, identify its possible determinants and evaluate it as disease biomarker we assessed the saccadic latency by electronystagmog
- PMID 21481421
- CELLULAR TOXICITY OF EXPANDED RNA REPEATS: FOCUS ON RNA FOCI.
- Wojciechowska M, Krzyzosiak WJ.SourceLaboratory of Cancer Genetics, Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, 61-704, Poland.
- Human molecular genetics.Hum Mol Genet.2011 Jul 4. [Epub ahead of print]
- Discrete and punctate nuclear RNA foci are characteristic molecular hallmarks of pathogenesis in myotonic dystrophy type 1 and type 2. Intranuclear RNA inclusions of distinct morphology have also been found in fragile X-associated tremor ataxia syndrome, Huntington's disease-like 2, spinocerebellar
- PMID 21729883
- Nucleolar Disruption and Cajal Body Disassembly are Nuclear Hallmarks of DNA Damage-Induced Neurodegeneration in Purkinje Cells.
- Baltanas FC, Casafont I, Weruaga E, Alonso JR, Berciano MT, Lafarga M.SourceLaboratory of Neural Plasticity and Neurorepair, Institute for Neuroscience of Castilla y Leon, Universidad de Salamanca, Salamanca, Spain. Department of Anatomy and Cell Biology and "Centro de Investigacion Biomedica en Red sobre Enfermedades Neurodegenerativas (CIBERNED)", University of Cantabria-IFIMAV, Santander, Spain. University of Tarapaca, Arica, Chile.
- Brain pathology (Zurich, Switzerland).Brain Pathol.2011 Jul;21(4):374-88. doi: 10.1111/j.1750-3639.2010.00461.x. Epub 2010 Nov 30.
- The Purkinje cell (PC) degeneration (pcd) phenotype results from mutation in nna1 gene and is associated with the degeneration and death of PCs during the postnatal life. Although the pcd mutation is a model of the ataxic mouse, it shares clinical and pathological characteristics of inherited human
- PMID 21054627
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
- 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
- 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
Related Links
- Spinocerebellar ataxia type 2 (SCA2) is characterized by progressive cerebellar ataxia, including nystagmus, slow saccadic eye movements and, in some individuals, ophthalmoparesis or parkinsonism. Pyramidal findings ...
- Spinocerebellar ataxia type 2 (SCA2) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with coordination and balance (ataxia). Other early signs and ...
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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
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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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