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Transcranial magnetic stimulation in hereditary ataxias: Diagnostic utility, pathophysiological insight and treatment

期刊

CLINICAL NEUROPHYSIOLOGY
卷 129, 期 8, 页码 1688-1698

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.clinph.2018.06.003

关键词

Transcranial magnetic stimulation; Hereditary ataxias; Spinocerebellar ataxias; Corticospinal tract; Diagnostic utility; Disease monitoring; Treatment

资金

  1. Cuban Ministry of Public Health
  2. Alexander von Humboldt Foundation

向作者/读者索取更多资源

Transcranial magnetic stimulation (TMS) is a valuable technique to assess and modulate human brain function in normal and pathological conditions. This critical review surveys the contributions of TMS to the diagnosis, insight into pathophysiology and treatment of genetically confirmed hereditary ataxias, a heterogeneous group of neurodegenerative disorders that can affect motor cortex and the corticospinal tract. Most studies were conducted on small sample sizes and focused on diagnostic approaches. The available data demonstrate early involvement of the corticospinal tract and motor cortex circuitry, and support the possible efficacy of cerebellar repetitive TMS (rTMS) as therapeutic approach. Further TMS-based studies are warranted, to establish biomarkers for early diagnosis and disease monitoring, explore the involvement of the cerebello-dentato-thalamo-cortical projection, study the effects of rTMS-induced plasticity, and utilize rTMS for treatment. (C) 2018 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rights reserved.

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