1998
DOI: 10.1016/s0022-510x(97)00209-8
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Non-familial olivopontocerebellar atrophy combined with late onset Alzheimer's disease: a clinico-pathological case report

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Cited by 8 publications

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“…The histopathological hallmark is the formation of α-synuclein-positive and Gallyas-positive argyrophilic glial cytoplasmic inclusions 2 9 10 11 12. The inclusions may be also stained with ubiquitin,9 as found in this case.…”
Section: Discussion
supporting
confidence: 51%
“…In support of the central mechanism, a histochemical study has confirmed severe loss of putative chemosensitive neurons, accumulation of α-synuclein immunoreactive glial inclusions as well as marked fibre gliosis in the medulla in cases of MSA 10 11 12. Additionally, given that autonomic failure is a prominent feature of MSA, a pathological involvement of autonomic neurons would contribute to respiratory arrest in MSA 3 4.…”
Section: Discussion
mentioning
confidence: 86%
“…However, the immunoreactivity was preserved for α-synuclein and ubiquitin, consistent with MSA. Aggregation of α-synuclein underlies α-synucleinopathies including MSA, Parkinson disease, dementia with Lewy bodies (LBs), diffuse LB disease and the LB variant of Alzheimer disease 9 10 11 12 13…”
Section: Discussion
mentioning
confidence: 99%
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