Marked laterality of olivopontocerebellar pathology in an autopsied patient with MSA: Implications for degeneration and α-synuclein propagation-Reference-Cited by-同舟云学术

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Marked laterality of olivopontocerebellar pathology in an autopsied patient with MSA: Implications for degeneration and α-synuclein propagation

Published:2023-11-21 Issue: Volume: Page:jnnp-2023-332419
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:J Neurol Neurosurg Psychiatry

Author:

Ozawa Misato^ORCID,Saito Rie^ORCID,Konno Takuya,Koide Reiji,Fujimoto Shigeru^ORCID,Onodera Osamu^ORCID,Kakita Akiyoshi

Funder

Japan Society for the Promotion of Science

CNS Degenerative Diseases, Research on Policy Planning and Evaluation for Rare and Intractable Diseases, Health, Labour and Welfare Sciences Research Grants

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

Reference6 articles.

1. What clinical features are most useful to distinguish definite multiple system atrophy from Parkinson's disease?

2. Marked asymmetry of Putaminal pathology in an MSA-P patient with Pisa syndrome;Hozumi;Mov Disord,2004

3. An autopsy case of Preclinical multiple system atrophy (MSA-C);Kon;Neuropathology,2013

4. Multiple system atrophy: α-synuclein and neuronal degeneration

5. The distribution and dynamic density of oligodendroglial cytoplasmic inclusions (GCIs) in multiple system atrophy: a correlation between the density of GCIs and the degree of involvement of striatonigral and olivopontocerebellar systems

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