Huntington's Disease
Language: English
Published by Oxford Univ Pr, 2014
Series: Book 13 of 21 - Oxford Monographs on Medical Genetics
- Hardcover
- New

Seller: Revaluation Books, Exeter, United KingdomRevaluation Books
AbeBooks seller since January 6, 2003
Condition: New
£ 382.04
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Add to basketItem description from seller
4th edition. 502 pages. 10.50x7.25x1.00 inches. In Stock.
Seller Inventory # 0199929149
- Title
- Huntington's Disease
- Author
- Bates, Gillian (Editor)/ Tabrizi, Sarah (Editor)/ Jones, Lesley (Editor)
- Publisher
- Oxford Univ Pr
- Publication year
- 2014
- Condition
- Brand New
- Binding
- Hardcover
- Language
- English
- ISBN 10
- 0199929149
- ISBN 13
- 9780199929146
- Edition
- 4th Edition
- Item weight
- 1.03 kilograms
- Series
- Book 13 of 21: Oxford Monographs on Medical Genetics
Completely updated and expanded, chapters in this volume are organized in five sections:
· Clinical aspects of Huntington's disease, including updated chapters on historical perspectives, neurological, neuropsychiatric, and neuropsychological aspects, and new chapters on juvenile Huntington's and the premanifest and early stages
· The genetics of Huntington's disease, including new information on its epidemiology discussions of new testing guidelines
· Neurobiology, including recent insights into correlations between pathology and symptoms and a new chapter on neuronal circuitry
· The molecular biology of Huntington's disease, including new chapters on the normal function of huntingtin, the molecular pathogenesis of Huntington's disease and the peripheral pathology of the disorder, and an extensively updated chapter on its structural biology
· An updated description of the comprehensive care for Huntington's disease, featureing a new chapter on preclinical therapeutics and a completely rewritten chapter on the state of the art of experimental therapeutics and clinical trials.
"Synopsis" may belong to another edition of this title.
About the Author
Professor Lesley Jones obtained her PhD from Cardiff University in 1990 and moved to the then University of Wales College of Medicine in 1994 to work on the biochemistry of huntingtin in HD. Her work has primarily been concerned with the notable downstream effects of mutant huntingtin on gene expression. She is also leading work on genetic modifiers of HD to assist in the identification of molecular pathways important in disease pathology.
Sarah Tabrizi is Professor of Clinical Neurology in the Department of Neurodegenerative Diseases at the UCL Institute of Neurology and Honorary Consultant Neurologist at the National Hospital of Neurology and Neurosurgery. Her research focuses on the pathobiological, translational and clinical aspects of neurodegeneration with a major focus on Huntington's disease. Sarah leads two major, international multidisciplinary research initiatives, TRACK-HD and Track-On HD, aimed at understanding the neurobiology of the neurodegenerative changes in premanifest and early stage HD gene carriers and identifying sensitive measures of disease progression.
"About the title" may belong to another edition of this title.
Revaluation Books
Exeter, United Kingdom
AbeBooks seller since January 6, 2003
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Edward Bowditch Ltd
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Exeter, United Kingdom EX3 0PP
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