<p>This detailed book provides a laboratory manual and guidebook for the selection, implementation, and interpretation of a wide range of techniques in contemporary use in leading laboratories engaged in Huntingtonβs disease (HD) research worldwide. Only by understanding the pathology and pathogenic
Huntington's Disease
β Scribed by Clay Farris Naff
- Publisher
- Greenhaven Publishing, LLC
- Year
- 2012
- Tongue
- English
- Series
- Perspectives on Diseases & Disorders
- Category
- Fiction
No coin nor oath required. For personal study only.
β¦ Synopsis
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 impaired coordination, slurred speech, and difficulty feeding and swallowing. Provide your readers with essential information on HD. This book also serves as a historical survey, by providing information on the controversies surrounding its causes. Compelling first-person narratives by people coping with Huntington's Disease give readers a first-hand experience. Patients, family members, or caregivers explain the condition from their own experience. The symptoms, causes, treatments, and potential cures are explained in detail. Essential to anyone trying to learn about diseases and conditions, the alternative treatments are explored. Student researchers and readers will find this book easily accessible through its careful and conscientious editing and a thorough introduction to each essay.
π SIMILAR VOLUMES
Huntington's disease is an incurable and fatal degenerative condition that robs people of normal brain function when they should be in the prime of life. This book describes the condition and the genetic causes behind it, follows researchers on their path to scientific discovery, identifies people w
It is now almost a decade since the identification of the Huntington's Disease gene and its mutation. Major advances in our understanding of the disorder have been made during this time. Since publication of the first two editions, much more extensive evidence exists on how the HD mutation actuall