Prevalence of Spinocerebellar Degenerations in the Hokuriku District in Japan

2009 ◽  
Vol 32 (3) ◽  
pp. 176-183 ◽  
Author(s):  
Ayumi Shibata-Hamaguchi ◽  
Chiho Ishida ◽  
Kazuo Iwasa ◽  
Masahito Yamada
Keyword(s):  
Spinocerebellar Degenerations

A CASE OF EXOGASTRIC GIANT LEIOMYOMA IN A PATIENT WITH SPINOCEREBELLAR DEGENERATIONS

1996 ◽  
Vol 57 (12) ◽  
pp. 3014-3018
Author(s):  
Kouji EMOTO ◽  
Masayoshi UENO ◽  
Toshifumi KANAIZUMI ◽  
Shiho SUGIMORI ◽  
Masami YAGI ◽  
...  
Keyword(s):  
Spinocerebellar Degenerations

scholarly journals Application of an Extended ADL Scale to Patients with Spinocerebellar Degenerations.

1995 ◽  
Vol 32 (1) ◽  
pp. 59-62
Author(s):  
Kenji KOSAKA ◽  
Ryuichi NAKAMURA ◽  
Masaaki FUJITA ◽  
Banri AMAKUSA ◽  
Toru HOSOKAWA
Keyword(s):  
Spinocerebellar Degenerations

Mitochondrial dysfunction and spinocerebellar degenerations

1986 ◽  
Vol 4 (1) ◽  
pp. 43-63 ◽  
Author(s):  
Jesse M. Cedarbaum ◽  
John P. Blass
Keyword(s):  
Mitochondrial Dysfunction ◽  
Spinocerebellar Degenerations

scholarly journals Dementia in Movement Disorders

1986 ◽  
Vol 13 (S4) ◽  
pp. 546-558 ◽  
Author(s):  
H. Teräväinen ◽  
M. Hietanen ◽  
J. Stoessl ◽  
D.B. Calne
Keyword(s):  
Cognitive Decline ◽  
Huntington's Disease ◽  
Progressive Supranuclear Palsy ◽  
Movement Disorders ◽  
Common Features ◽  
Wide Range ◽  
Clinicopathological Correlations ◽  
Spinocerebellar Degenerations ◽  
Cortical Pathology ◽  
Differential Involvement

Abstract:Of all the movement disorders, Huntington's disease has been most consistently associated with dementia, while it is only over the last decade that intellectual and cognitive decline have been recognized as common features of Parkinson's disease. It is now known that the pathology in these two conditions reflects differential involvement of the striatum. The Huntington lesion is primarily in the caudate, while the Parkinson lesion preferentially affects the putamen. Both conditions have more diffuse pathology, and dementia may also occur in a wide range of other extrapyramidal diseases, such as progressive supranuclear palsy, the parkinsonism-dementia complex of Guam, and certain spinocerebellar degenerations. Clinicopathological correlations will be reviewed in these disorders of primarily subcortical pathology, and comparisons will be made with Alzheimer's disease, a disorder of predominantly cortical pathology.

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