Literature DB >> 16773505

Functional MRI reveals activation of a subcortical network in a 5-year-old girl with genetically confirmed myoclonus-dystonia.

M F Nitschke1, C Erdmann, P Trillenberg, A Sprenger, N Kock, J Sperner, C Klein.   

Abstract

We investigated a five-year-old girl suffering from genetically confirmed, action-induced myoclonus-dystonia (M-D) with functional magnetic resonance imaging (MRI). We compared the activation pattern by movements of her right hand as if drawing a picture, which elicited M-D, with simple snapping movements (without overt M-D). The drawing and snapping conditions resulted in activation of a motor network including the motor cortex, the putamen, and the cerebellar hemispheres. The direct comparison of the drawing condition with snapping as control revealed specific activations within the thalamus and the dentate nucleus. An age matched healthy control did not show significant activation within the thalamus or dentate nucleus.

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Year:  2006        PMID: 16773505     DOI: 10.1055/s-2006-924109

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  8 in total

Review 1.  Alternative approaches to modeling hereditary dystonias.

Authors:  Rachel Fremont; Kamran Khodakhah
Journal:  Neurotherapeutics       Date:  2012-04       Impact factor: 7.620

Review 2.  It's not just the basal ganglia: Cerebellum as a target for dystonia therapeutics.

Authors:  Ambika Tewari; Rachel Fremont; Kamran Khodakhah
Journal:  Mov Disord       Date:  2017-08-26       Impact factor: 10.338

3.  SGCE isoform characterization and expression in human brain: implications for myoclonus-dystonia pathogenesis?

Authors:  Katja Ritz; Barbera Dc van Schaik; Marja E Jakobs; Antoine H van Kampen; Eleonora Aronica; Marina A Tijssen; Frank Baas
Journal:  Eur J Hum Genet       Date:  2010-12-15       Impact factor: 4.246

Review 4.  Structural and functional magnetic resonance imaging of the human cerebellar nuclei.

Authors:  Michael Küper; Markus Thürling; Stefan Maderwald; Mark E Ladd; Dagmar Timmann
Journal:  Cerebellum       Date:  2012-06       Impact factor: 3.847

5.  Clinical and neurophysiological improvement of SGCE myoclonus-dystonia with GPi deep brain stimulation.

Authors:  Monica M Kurtis; Marta San Luciano; Qiping Yu; Robert R Goodman; Blair Ford; Deborah Raymond; Seth L Pullman; Rachel Saunders-Pullman
Journal:  Clin Neurol Neurosurg       Date:  2009-11-05       Impact factor: 1.876

6.  Deep brain stimulation for myoclonus-dystonia syndrome with double mutations in DYT1 and DYT11.

Authors:  Jia-Wei Wang; Ji-Ping Li; Yun-Peng Wang; Xiao-Hua Zhang; Yu-Qing Zhang
Journal:  Sci Rep       Date:  2017-01-19       Impact factor: 4.379

7.  Acute cerebellar knockdown of Sgce reproduces salient features of myoclonus-dystonia (DYT11) in mice.

Authors:  Samantha Washburn; Rachel Fremont; Maria Camila Moreno-Escobar; Chantal Angueyra; Kamran Khodakhah
Journal:  Elife       Date:  2019-12-23       Impact factor: 8.140

8.  Speech-activated Myoclonus Mimicking Stuttering in a Patient with Myoclonus-Dystonia Syndrome.

Authors:  David A Isaacs; Peter Hedera
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2016-07-01
  8 in total

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