@article{695423,
      recid = {695423},
      author = {Wenning, Gregor K., and Fanciulli, Alessandra,},
      title = {Multiple system atrophy [electronic resource]  /},
      pages = {1 online resource (xvi, 198 pages) :},
      note = {Includes index.},
      abstract = {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.},
      url = {http://library.usi.edu/record/695423},
      doi = {https://doi.org/10.1007/978-3-7091-0687-7},
}