Corpus ID: 8898819

Symptomatic Treatment and Management of Huntington's Disease: An Overview

@inproceedings{Tyagi2010SymptomaticTA,
  title={Symptomatic Treatment and Management of Huntington's Disease: An Overview},
  author={L. Tyagi and R. Shekhar and M. Singh and M. Nagar},
  year={2010}
}
5 Abstract: Huntington's disease (HD) is an inherited disease of the central nervous system that usually has its onset between 30 and 50 years of age. The patient has progressive dementia with bizarre involvantary movements of chorea. The disease slowly progresses and death is usually due to an intercurrent infection. Huntington's disease affects someone's ability to think, talk and move by destroying cells in the basal ganglia, the part of the brain that controls these capacities. A patient… Expand
Huntington’s Disease: The Search for Therapeutic Agents
HUNTINGTON GENE ONTOLOGICAL STUDY AND ORTHOLOGICAL ANALYSIS
Computational Drug Repositioning with Random Walk on a Heterogeneous Network

References

SHOWING 1-10 OF 23 REFERENCES
Huntington's disease
Huntington's disease
The functional anatomy of basal ganglia disorders
The
Iron in neurodegenerative disorders
Neurodegenerative Disorders
Spared Subset of Striatal Neurons in Huntington's Disease
  • J. Neuropathol. Exp. Neurol
  • 2006
Monoamine Decreasing Drugs with Psychiatric
  • Management of Parkinsonism USA,
  • 2004
...
1
2
3
...