Multiple system atrophy [electronic resource] / Gregor Wenning, Alessandra Fanciulli, editors.
2013
RC394.D35 .M85 2013
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Title
Multiple system atrophy [electronic resource] / Gregor Wenning, Alessandra Fanciulli, editors.
ISBN
9783709106877 electronic book
3709106877 electronic book
9783709106860
3709106877 electronic book
9783709106860
Published
Vienna : Springer, [2013?]
Copyright
©2014
Language
English
Description
1 online resource (xvi, 198 pages) : color illustrations.
Item Number
10.1007/978-3-7091-0687-7 doi
Call Number
RC394.D35 .M85 2013
Dewey Decimal Classification
616.8
Summary
This textbook provides a comprehensive monography on multiple system atrophy (MSA), a rare and fatal neurodegenerative disorder that presents with autonomic failure and either parkinsonism (MSA-P) or cerebellar ataxia (MSA-C).The underlying neuropathology of MSA is characterized by striatonigral degeneration (SND), olivopontocerebellar atrophy (OPCA) and unique oligodendroglial cytoplasmic alpha-synuclein inclusions. MSA is therefore classified among the alpha-synucleinopathies such as Parkinson's disease, pure autonomic failure and dementia with Lewy bodies. Over the last decade there have been important advances in early diagnosis, pathogenesis research and clinical trial activity. The monography will cover the entire spectrum ranging from molecular and genetic work to symptomatic and interventional therapies. The book is written for movement disorder clinicians and basic neuroscientists interested in degenerative movement disorders.
Note
Includes index.
Access Note
Access limited to authorized users.
Source of Description
Description based on online resource; title from PDF title page (SpringerLink, viewed Sep. 26, 2013).
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Table of Contents
1. Historical Review
2. Epidemiology
3. Neuropathology
4. Etiopathogenesis
5. Animal Models
6. Clinical Presentation
7. Clinical diagnostic Criteria
8. Natural History
9. Investigations
10. Treatment.
2. Epidemiology
3. Neuropathology
4. Etiopathogenesis
5. Animal Models
6. Clinical Presentation
7. Clinical diagnostic Criteria
8. Natural History
9. Investigations
10. Treatment.