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1962 21
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1965 31
1966 20
1967 19
1968 25
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1970 26
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2007 264
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2009 261
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Page 1
Spinocerebellar degeneration.
Perlman SL. Perlman SL. Expert Opin Pharmacother. 2003 Oct;4(10):1637-41. doi: 10.1517/14656566.4.10.1637. Expert Opin Pharmacother. 2003. PMID: 14521474 Review.
The spinocerebellar degenerations/ataxias (SCAs) are a diverse group of rare, slowly progressive, neurological diseases, often inherited but of incompletely understood pathophysiology, which affect the cerebellum and its related pathways. ...
The spinocerebellar degenerations/ataxias (SCAs) are a diverse group of rare, slowly progressive, neurological diseases, often …
[Treatment for Spinocerebellar Degeneration].
Matsushima M, Yabe I. Matsushima M, et al. Brain Nerve. 2023 May;75(5):498-502. doi: 10.11477/mf.1416202366. Brain Nerve. 2023. PMID: 37194519 Japanese.
No disease-modifying therapy has been established for spinocerebellar degeneration and multiple system atrophy, and only symptomatic therapy is currently available. ...Muscle relaxants are used for spasticity associated with spinocerebellar degeneration …
No disease-modifying therapy has been established for spinocerebellar degeneration and multiple system atrophy, and only sympt …
[Spinocerebellar Degeneration: One Liter of Tears].
Sasaki H. Sasaki H. Brain Nerve. 2022 Dec;74(12):1402-1404. doi: 10.11477/mf.1416202259. Brain Nerve. 2022. PMID: 36503144 Japanese.
This movie, based on the diary of a girl affected with juvenile onset of spinocerebellar ataxia, begins at the age of 13, when she first showed unstable gait. ...
This movie, based on the diary of a girl affected with juvenile onset of spinocerebellar ataxia, begins at the age of 13, when she fi …
Cognitive impairment in spinocerebellar degeneration.
Kawai Y, Suenaga M, Watanabe H, Sobue G. Kawai Y, et al. Eur Neurol. 2009;61(5):257-68. doi: 10.1159/000206850. Epub 2009 Mar 17. Eur Neurol. 2009. PMID: 19295212 Free article. Review.
It has been reported that patients with spinocerebellar degenerations (SCDs) have cognitive dysfunction as well as limb and truncal ataxia, dysarthria and dysphagia. ...Although there are few comparison studies among the various SCDs, cognitive dysfunction may be mo …
It has been reported that patients with spinocerebellar degenerations (SCDs) have cognitive dysfunction as well as limb and tr …
[Neurorehabilitation for spinocerebellar degeneration].
Miyai I. Miyai I. Rinsho Shinkeigaku. 2013;53(11):931-3. doi: 10.5692/clinicalneurol.53.931. Rinsho Shinkeigaku. 2013. PMID: 24291837 Review. Japanese.
It remains to be elucidated whether there is a use- or dose-dependent effect of rehabilitative intervention on impairment and disability of spinocerebellar degeneration since the disease progressively damages cerebellar structure that plays a crucial role in motor l …
It remains to be elucidated whether there is a use- or dose-dependent effect of rehabilitative intervention on impairment and disability of …
[Spinocerebellar degeneration-corneal dystrophy].
Ito M, Sugie H. Ito M, et al. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):675-6. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528959 Review. Japanese. No abstract available.
[Recent clinical advances in hereditary spinocerebellar degeneration].
Yabe I. Yabe I. Rinsho Shinkeigaku. 2024 Mar 22;64(3):135-147. doi: 10.5692/clinicalneurol.cn-001931. Epub 2024 Feb 22. Rinsho Shinkeigaku. 2024. PMID: 38382935 Review. Japanese.
Spinocerebellar degeneration (SCD) is a neurodegenerative disorder characterized by cerebellar ataxia and other multisystem manifestations, such as Parkinsonism and pyramidal tract symptoms. ...
Spinocerebellar degeneration (SCD) is a neurodegenerative disorder characterized by cerebellar ataxia and other multisystem ma …
Clinicopathology of spinocerebellar degeneration: its correlation to the unstable CAG repeat of the affected gene.
Yagishita S, Inoue M. Yagishita S, et al. Pathol Int. 1997 Jan;47(1):1-15. doi: 10.1111/j.1440-1827.1997.tb04429.x. Pathol Int. 1997. PMID: 9051687 Review.
A third gene locus is assigned to the short arm of chromosome 12 (12p2-pter) causing dentatorubropallidoluysian atrophy (DRPLA). The gene for spinocerebellar ataxia type 2 (SCA2) is located in the 12q23-24. Subsequently, a sporadic counterpart of hereditary olivopontocereb …
A third gene locus is assigned to the short arm of chromosome 12 (12p2-pter) causing dentatorubropallidoluysian atrophy (DRPLA). The gene fo …
Spinocerebellar degeneration: Discrepancies between clinical and pathological diagnoses.
Yamada M, Toyoshima Y, Makifuchi T, Kakita A, Takahashi H. Yamada M, et al. Neuropathology. 2016 Aug;36(4):405-10. doi: 10.1111/neup.12278. Epub 2015 Nov 11. Neuropathology. 2016. PMID: 26556659
To improve the diagnostic accuracy of sporadic spinocerebellar degeneration (SCD), we assessed the clinical and pathological data of 1494 consecutive autopsy cases. ...
To improve the diagnostic accuracy of sporadic spinocerebellar degeneration (SCD), we assessed the clinical and pathological d …
[The Nomenclature and Classification of Sporadic Spinocerebellar Degeneration].
Koga S. Koga S. Brain Nerve. 2016 Dec;68(12):1453-1457. doi: 10.11477/mf.1416200616. Brain Nerve. 2016. PMID: 27916755 Review. Japanese.
Spinocerebellar degeneration (SCD) is a neurodegenerative disease characterized by progressive cerebellar ataxia. ...
Spinocerebellar degeneration (SCD) is a neurodegenerative disease characterized by progressive cerebellar ataxia. ...
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