Literature DB >> 15293281

Microstructural white matter changes in carriers of the DYT1 gene mutation.

Maren Carbon1, Peter B Kingsley, Sherwin Su, Gwenn S Smith, Phoebe Spetsieris, Susan Bressman, David Eidelberg.   

Abstract

We tested the hypothesis that the DYT1 genotype is associated with a disorder of anatomical connectivity involving primarily the sensorimotor cortex. We used diffusion tensor magnetic resonance imaging (DTI) to assess the microstructure of white matter pathways in mutation carriers and control subjects. Fractional anisotropy (FA), a measure of axonal integrity and coherence, was reduced (p < 0.005) in the subgyral white matter of the sensorimotor cortex of DYT1 carriers. Abnormal anatomical connectivity of the supplementary motor area may contribute to the susceptibility of DYT1 carriers to develop clinical manifestations of dystonia. Copyright 2004 American Neurological Association

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Year:  2004        PMID: 15293281     DOI: 10.1002/ana.20177

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  45 in total

Review 1.  Genetic and clinical features of primary torsion dystonia.

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Review 2.  Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.

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3.  Microstructural white matter changes in primary torsion dystonia.

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4.  Increased cerebellar activation during sequence learning in DYT1 carriers: an equiperformance study.

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Review 7.  The functional neuroanatomy of dystonia.

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Review 8.  The evolving role of diffusion magnetic resonance imaging in movement disorders.

Authors:  Christopher W Hess; Edward Ofori; Umer Akbar; Michael S Okun; David E Vaillancourt
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9.  Effects of cerebellar TMS on motor cortex of patients with focal dystonia: a preliminary report.

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Review 10.  Current role of functional MRI in the diagnosis of movement disorders.

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Journal:  Neuroimaging Clin N Am       Date:  2010-02       Impact factor: 2.264

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