9780521811668-052181166X-Neurodegenerative Diseases: Neurobiology, Pathogenesis and Therapeutics

Neurodegenerative Diseases: Neurobiology, Pathogenesis and Therapeutics

ISBN-13: 9780521811668
ISBN-10: 052181166X
Edition: 1
Author: Anthony E. Lang, Albert C. Ludolph, M. Flint Beal
Publication date: 2005
Publisher: Cambridge University Press
Format: Hardcover 1008 pages
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Book details

ISBN-13: 9780521811668
ISBN-10: 052181166X
Edition: 1
Author: Anthony E. Lang, Albert C. Ludolph, M. Flint Beal
Publication date: 2005
Publisher: Cambridge University Press
Format: Hardcover 1008 pages

Summary

Neurodegenerative Diseases: Neurobiology, Pathogenesis and Therapeutics (ISBN-13: 9780521811668 and ISBN-10: 052181166X), written by authors Anthony E. Lang, Albert C. Ludolph, M. Flint Beal, was published by Cambridge University Press in 2005. With an overall rating of 3.5 stars, it's a notable title among other books. You can easily purchase or rent Neurodegenerative Diseases: Neurobiology, Pathogenesis and Therapeutics (Hardcover) from BooksRun, along with many other new and used books and textbooks. And, if you're looking to sell your copy, our current buyback offer is $0.53.

Description

Neurodegenerative diseases are major contributors to disability and disease, with Alzheimer's and Parkinson's diseases the most prevalent. This major reference reviews the rapidly advancing knowledge of pathogenesis and treatment of neurodegenerative diseases in the context of a comprehensive survey of each disease and its clinical features. The editors and contributors are among the leading experts in the field internationally. Covering basic science, diagnostic tools and therapeutic approaches, the book focuses on all aspects of neurodegenerative disease, including the normal aging process. The dementias, prion diseases, Parkinson's disease and atypical parkinsonisms, neurodegenerative ataxias, motor neuron diseases, degenerative diseases with chorea, iron and copper disorders, and mitochondrial diseases, are all methodically presented and discussed, with extensive illustrations. In each case the underlying genetics, neuropathological and clinical issues are fully reviewed, making this the most complete as well as the most authoritative reference available to clinicians and neuroscientists.

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