spinocerebellar ataxia type 2

出典: meddic

脊髄小脳失調症2型

dominantly-inherited spinocerebellar ataxiaspinocerebellar ataxiaspinocerebellar ataxia type 1spinocerebellar ataxia type 4spinocerebellar ataxia type 5spinocerebellar ataxia type 6spinocerebellar ataxia type 7spinocerebellar atrophy

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英文文献

  • 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

和文文献

  • 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

関連リンク

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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★リンクテーブル★
先読みspinocerebellar ataxia
リンク元spinocerebellar ataxia type 1」「spinocerebellar ataxia type 4」「spinocerebellar ataxia type 6」「spinocerebellar ataxia type 7」「spinocerebellar ataxia type 5
関連記事type」「ataxia」「typing」「spinocerebellar ataxia」「typed

spinocerebellar ataxia」

  [★] 脊髄小脳変性症 spinocerebellar degeneration SCD = SCA


spinocerebellar ataxia type 1」

  [★]

脊髄小脳失調症1型脊髄小脳変性症1型

dominantly-inherited spinocerebellar ataxiaSCA1spinocerebellar ataxiaspinocerebellar ataxia type 2spinocerebellar ataxia type 4spinocerebellar ataxia type 5spinocerebellar ataxia type 6spinocerebellar ataxia type 7spinocerebellar atrophy


spinocerebellar ataxia type 4」

  [★]

脊髄小脳失調症4型

dominantly-inherited spinocerebellar ataxiaspinocerebellar ataxiaspinocerebellar ataxia type 1spinocerebellar ataxia type 2spinocerebellar ataxia type 5spinocerebellar ataxia type 6spinocerebellar ataxia type 7spinocerebellar atrophy


spinocerebellar ataxia type 6」

  [★]

脊髄小脳失調症6型

dominantly-inherited spinocerebellar ataxiaspinocerebellar ataxiaspinocerebellar ataxia type 1spinocerebellar ataxia type 2spinocerebellar ataxia type 4spinocerebellar ataxia type 5spinocerebellar ataxia type 7spinocerebellar atrophy


spinocerebellar ataxia type 7」

  [★]

脊髄小脳失調症7型

dominantly-inherited spinocerebellar ataxiaspinocerebellar ataxiaspinocerebellar ataxia type 1spinocerebellar ataxia type 2spinocerebellar ataxia type 4spinocerebellar ataxia type 5spinocerebellar ataxia type 6spinocerebellar atrophy


spinocerebellar ataxia type 5」

  [★]

脊髄小脳失調症5型

dominantly-inherited spinocerebellar ataxiaspinocerebellar ataxiaspinocerebellar ataxia type 1spinocerebellar ataxia type 2spinocerebellar ataxia type 4spinocerebellar ataxia type 6spinocerebellar ataxia type 7spinocerebellar 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
formmodepatterntype specimentyped

WordNet   license wordnet

「write by means of a keyboard with types; "type the acceptance letter, please"」
typewrite

WordNet   license wordnet

「(biology) the taxonomic group whose characteristics are used to define the next higher taxon」

WordNet   license wordnet

「a subdivision of a particular kind of thing; "what type of sculpture do you prefer?"」

WordNet   license wordnet

「all of the tokens of the same symbol; "the word `element'' contains five different types of character"」

WordNet   license wordnet

「printed characters; "small type is hard to read"」

PrepTutorEJDIC   license prepejdic

「〈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」

WordNet   license wordnet

「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"」

WordNet   license wordnet

「identify as belonging to a certain type; "Such people can practically be typed"」
typecast


ataxia」

  [★] 運動失調

WordNet   license wordnet

「inability to coordinate voluntary muscle movements; unsteady movements and staggering gait」
ataxy, dyssynergia, motor ataxia

typing」

  [★]

  • n.
  • タイプで打つこと、タイピング。分類


WordNet   license wordnet

「writing done with a typewriter」
typewriting


spinocerebellar ataxia」

  [★] 脊髄小脳変性症 spinocerebellar degeneration SCD = SCA


typed」

  [★]

  • adj.
  • 型の
formmodepatterntype




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