| 書目名稱 | Multiple System Atrophy |
| 編輯 | Gregor K. Wenning,Alessandra Fanciulli |
| 視頻video | http://file.papertrans.cn/642/641048/641048.mp4 |
| 概述 | Provides complete insight into onset, progression, diagnoses and therapy of MSA.Summarizes the important advances gained in the last years in MSA research.Describes novel findings in MSA research and |
| 圖書封面 |  |
| 描述 | 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. |
| 出版日期 | Book 2014 |
| 關(guān)鍵詞 | Alpha-synucleinopathies; Movement Disorders; Neurodegeneration; Parkinson′s Disease; Substantia Nigra |
| 版次 | 1 |
| doi | https://doi.org/10.1007/978-3-7091-0687-7 |
| isbn_softcover | 978-3-7091-2010-1 |
| isbn_ebook | 978-3-7091-0687-7 |
| copyright | Springer-Verlag Wien 2014 |
|Archiver|手機版|小黑屋|
派博傳思國際
( 京公網(wǎng)安備110108008328)
GMT+8, 2025-10-25 10:10
發(fā)表于 2025-3-21 19:45:28
