𝔖 Bobbio Scriptorium
✦   LIBER   ✦

the management of Huntington's disease


Book ID
111196008
Publisher
BMJ Publishing Group
Year
2004
Tongue
English
Weight
179 KB
Volume
4
Category
Article
ISSN
1474-7758

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πŸ“œ SIMILAR VOLUMES


The current clinical management of Hunti
✍ Wendy Phillips; Kathleen M. Shannon; Roger A. Barker πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 225 KB

## Abstract Huntington's disease is a neurodegenerative condition, characterized by movement disorders, cognitive decline, and psychiatric disturbance. We review the pharmacological management of the various movement disorders associated with the disease, the cognitive decline and the commonly enco

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Huntington's disease (HD) is a late-onset degenerative disorder of the central nervous system, caused by a dominantly inherited mutation in a gene on chromosome 4p. The identification of the trinucleotide repeat mutation responsible for this disorder has been an important step towards understanding

Huntington’s Disease
✍ Marcy E. MacDonald; Silvia Gines; James F. Gusella; Vanessa C. Wheeler πŸ“‚ Article πŸ“… 2003 πŸ› Humana Press Inc 🌐 English βš– 267 KB
Huntington's Disease
✍ Clay Farris Naff πŸ“‚ Fiction πŸ“… 2012 πŸ› Greenhaven Publishing, LLC 🌐 en-US βš– 4 MB

Huntington's Disease causes degeneration of brain cells, in motor control regions of the brain, as well as other areas. Symptoms get progressively worse, and include uncontrolled movements, abnormal body postures, and changes in emotion, behavior, judgment, and cognition. People with HD also develop