Structural Changes Associated with Progression of Motor Deficits in Spinocerebellar Ataxia 17

@article{Reetz2009StructuralCA,
  title={Structural Changes Associated with Progression of Motor Deficits in Spinocerebellar Ataxia 17},
  author={Kathrin Reetz and Rebekka Lencer and Johannes M. Hagenah and Christian Gaser and Vera Tadi{\'c} and Uwe Walter and Alexander Wolters and Susanne Steinlechner and Christine Z{\"u}hlke and Katja Brockmann and Christine Klein and Arndt Rolfs and Ferdinand Binkofski},
  journal={The Cerebellum},
  year={2009},
  volume={9},
  pages={210-217}
}
Spinocerebellar ataxia (SCA17) is a rare genetic disorder characterized by a variety of neuropsychiatric symptoms. Recently, using magnetic resonance imaging (MRI) voxel-based morphometry (VBM), several specific functional–structural correlations comprising differential degeneration related to motor and psychiatric symptoms were reported in patients with SCA17. To investigate gray matter volume (GMV) changes over time and its association to clinical neuropsychiatric symptomatology, nine SCA17… CONTINUE READING

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References

Publications referenced by this paper.
SHOWING 1-10 OF 38 REFERENCES

Spinocerebellar ataxia type 17 is caused by mutations in the TATA-box binding protein

Christine Zühlke, Katrin Bürk
  • The Cerebellum
  • 2007
VIEW 1 EXCERPT

Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17.

  • Movement disorders : official journal of the Movement Disorder Society
  • 2006
VIEW 1 EXCERPT

Spinocerebellar Ataxia 17 and Huntington's disease-like 4. Genetic instabilities, neurological diseases

R Wells, T Ashizawa
  • 2006
VIEW 1 EXCERPT