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  • 1-10 ل  79 نتائج ل ""Spinocerebellar Ataxias""

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Subject : brain
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Academic Journal

Neuropathology of SCA34 showing widespread oligodendroglial pathology with vacuolar white matter degeneration: a case study.

  • Authors : Ozaki K; Department of Neurology and Neurological Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo, Japan. .; Laboratory for Comprehensive Genomic Analysis, RIKEN Center for Integrative Medical Sciences, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa, Japan. .

Subjects: Brain/Brain/Brain/*pathology ; Nerve Degeneration/Nerve Degeneration/Nerve Degeneration/*pathology ; Oligodendroglia/Oligodendroglia/Oligodendroglia/*pathology

  • Source: Acta neuropathologica communications [Acta Neuropathol Commun] 2021 Oct 24; Vol. 9 (1), pp. 172. Date of Electronic Publication: 2021 Oct 24.Publisher: BioMed Central Country of Publication: England NLM ID: 101610673 Publication Model: Electronic Cited Medium: Internet ISSN: 2051-5960

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Academic Journal

In vivo microstructural white matter changes in early spinocerebellar ataxia 2.

  • Authors : Stezin A; Department of Clinical Neurosciences, Department of Neurology, National Institute of Mental Health & Neurosciences (NIMHANS), Bangalore, India.; Bhardwaj S

Subjects: Brain/Brain/Brain/*pathology ; Spinocerebellar Ataxias/Spinocerebellar Ataxias/Spinocerebellar Ataxias/*pathology ; White Matter/White Matter/White Matter/*pathology

  • Source: Acta neurologica Scandinavica [Acta Neurol Scand] 2021 Mar; Vol. 143 (3), pp. 326-332. Date of Electronic Publication: 2020 Nov 04.Publisher: Wiley-Blackwell Country of Publication: Denmark NLM ID: 0370336 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Spinocerebellar ataxias.

  • Authors : Mascalchi M; Radiodiagnostic Section, Department of Clinical Physiopathology, University of Florence, 50134 Florence, Italy.

Subjects: Magnetic Resonance Imaging*; Brain/Brain/Brain/*pathology ; Spinocerebellar Ataxias/Spinocerebellar Ataxias/Spinocerebellar Ataxias/*pathology

  • Source: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2008 Oct; Vol. 29 Suppl 3, pp. 311-3.Publisher: Springer-Verlag Italia Country of Publication: Italy NLM ID: 100959175 Publication Model: Print Cited Medium: Print ISSN: 1590-1874

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Academic Journal

Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseases.

  • Authors : Tachikawa M; Division of Functional Genomics, Department of Post-Genomics and Diseases, Osaka University Graduate School of Medicine, 2-2-B9 Yamadaoka, Suita, Osaka 565-0871, Japan.; Nagai Y

Subjects: Brain/Brain/Brain/*metabolism ; Neurodegenerative Diseases/Neurodegenerative Diseases/Neurodegenerative Diseases/*genetics ; Spinocerebellar Ataxias/Spinocerebellar Ataxias/Spinocerebellar Ataxias/*genetics

  • Source: Journal of human genetics [J Hum Genet] 2002; Vol. 47 (6), pp. 275-8.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print Cited Medium: Print ISSN: 1434-5161 (Print)

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Academic Journal

Autopsy case of spinocerebellar ataxia type 31 with severe dementia at the terminal stage.

  • Authors : Adachi T; Division of Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, Japan.; Kitayama M

Subjects: Brain/Brain/Brain/*pathology ; Dementia/Dementia/Dementia/*pathology ; Spinocerebellar Ataxias/Spinocerebellar Ataxias/Spinocerebellar Ataxias/*pathologySpinocerebellar Ataxia 31

  • Source: Neuropathology : official journal of the Japanese Society of Neuropathology [Neuropathology] 2015 Jun; Vol. 35 (3), pp. 273-9. Date of Electronic Publication: 2014 Dec 11.Publisher: Blackwell Science Asia Country of Publication: Australia NLM ID: 9606526 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31.

  • Authors : Ohmori H; a Department of Neurology , Yamaga Chuo Hospital , Yamaga City, Kumamoto , Japan.; Hara A

Subjects: Brain/Brain/Brain/*pathology ; Calcium Channels/Calcium Channels/Calcium Channels/*genetics ; Spinocerebellar Ataxias/Spinocerebellar Ataxias/Spinocerebellar Ataxias/*genetics

  • Source: Journal of neurogenetics [J Neurogenet] 2015; Vol. 29 (2-3), pp. 80-4. Date of Electronic Publication: 2015 Jul 13.Publisher: Informa Healthcare Country of Publication: England NLM ID: 8406473 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Cerebellar cognitive affective syndrome and autosomal recessive spastic ataxia of charlevoix-saguenay: a report of two male sibs.

  • Authors : Verhoeven WM; Vincent van Gogh Institute for Psychiatry, Centre of Excellence for Neuropsychiatry, Venray, The Netherlands. ; Egger JI

Subjects: Brain/Brain/Brain/*pathology ; Cerebellar Diseases/Cerebellar Diseases/Cerebellar Diseases/*diagnosis ; Cognition Disorders/Cognition Disorders/Cognition Disorders/*diagnosis Spastic ataxia Charlevoix-Saguenay type

  • Source: Psychopathology [Psychopathology] 2012; Vol. 45 (3), pp. 193-9. Date of Electronic Publication: 2012 Mar 22.Publisher: S. Karger Country of Publication: Switzerland NLM ID: 8401537 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Spinocerebellar ataxia type 7 (SCA7): widespread brain damage in an adult-onset patient with progressive visual impairments in comparison with an adult-onset patient without visual impairments.

  • Authors : Rüb U; Institute for Clinical Neuroanatomy, J. W. Goethe-University, Frankfurt/Main, Germany. ; Brunt ER

Subjects: Brain/Brain/Brain/*pathology ; Retina/Retina/Retina/*pathology ; Spinocerebellar Ataxias/Spinocerebellar Ataxias/Spinocerebellar Ataxias/*pathology

  • Source: Neuropathology and applied neurobiology [Neuropathol Appl Neurobiol] 2008 Apr; Vol. 34 (2), pp. 155-68. Date of Electronic Publication: 2007 Oct 26.Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 7609829 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Topography of cerebral monoamine transporter availability in families with SCA2 mutations: a voxel-wise [123I]beta-CIT SPECT analysis.

  • Authors : Scherfler C; Department of Neurology, Innsbruck Medical University, Anichstrasse 35, 6020 Innsbruck, Austria. ; Boesch SM

Subjects: Mutation*; Brain/Brain/Brain/*diagnostic imaging ; Brain/Brain/Brain/*metabolism

  • Source: European journal of nuclear medicine and molecular imaging [Eur J Nucl Med Mol Imaging] 2006 Sep; Vol. 33 (9), pp. 1084-90. Date of Electronic Publication: 2006 May 13.Publisher: Springer-Verlag Berlin Country of Publication: Germany NLM ID: 101140988 Publication Model: Print-Electronic Cited Medium: Print ISSN:

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Academic Journal

Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goes beyond the known brain predilection sites.

  • Authors : Gierga K; Institute of Clinical Neuroanatomy, J. W. Goethe University, Frankfurt/Main, Germany.; Schelhaas HJ

Subjects: Brain/Brain/Brain/*pathology ; Nerve Degeneration/Nerve Degeneration/Nerve Degeneration/*pathology ; Spinocerebellar Ataxias/Spinocerebellar Ataxias/Spinocerebellar Ataxias/*pathology

  • Source: Neuropathology and applied neurobiology [Neuropathol Appl Neurobiol] 2009 Oct; Vol. 35 (5), pp. 515-27. Date of Electronic Publication: 2009 Jan 30.Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 7609829 Publication Model: Print-Electronic Cited Medium: Internet

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  • 1-10 ل  79 نتائج ل ""Spinocerebellar Ataxias""