Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family.
about
The genetics and neuropathology of Parkinson's diseaseParkinsonism in spinocerebellar ataxiaAllele-specific RNA silencing of mutant ataxin-3 mediates neuroprotection in a rat model of Machado-Joseph disease.Analysis of Nigerians with apparently sporadic Parkinson disease for mutations in LRRK2, PRKN and ATXN3.Parkinsonian phenotype in Machado-Joseph disease (MJD/SCA3): a two-case report.SCA2 and SCA3 mutations in young-onset dopa-responsive parkinsonism.Genetics of parkinsonism.Genetic neuropathology of Parkinson's disease.Rapid genetic diagnosis in single-gene movement disordersLarge-scale assessment of polyglutamine repeat expansions in Parkinson diseaseMachado-Joseph disease/spinocerebellar ataxia type 3.Caring for Machado-Joseph disease: current understanding and how to help patients.Movement disorders in spinocerebellar ataxias.Tremor-spectrum in spinocerebellar ataxia type 3.Ataxin-3 and its e3 partners: implications for machado-joseph disease.Nonmotor and extracerebellar features in Machado-Joseph disease: a review.Advances in the genetics of Parkinson disease.Spinocerebellar ataxia type 3: subphenotypes in a cohort of Brazilian patients.Silencing ataxin-3 mitigates degeneration in a rat model of Machado-Joseph disease: no role for wild-type ataxin-3?Striatal and nigral pathology in a lentiviral rat model of Machado-Joseph disease.Caffeine and adenosine A(2A) receptor inactivation decrease striatal neuropathology in a lentiviral-based model of Machado-Joseph disease.Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and parkin gene mutations.Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and Caucasians.Overexpression of mutant ataxin-3 in mouse cerebellum induces ataxia and cerebellar neuropathology.To Dement or Not to Dement, That Is the Question.The BAG2 and BAG5 proteins inhibit the ubiquitination of pathogenic ataxin3-80Q.Does degeneration of the subthalamic nucleus prevent parkinsonism in spinocerebellar ataxia type 2 and type 3?No parkinsonism in SCA2 and SCA3 despite severe neurodegeneration of the dopaminergic substantia nigra.
P2860
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P2860
Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family.
description
2001 nî lūn-bûn
@nan
2001 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Spinocerebellar ataxia type 3 ...... son disease in a black family.
@ast
Spinocerebellar ataxia type 3 ...... son disease in a black family.
@en
type
label
Spinocerebellar ataxia type 3 ...... son disease in a black family.
@ast
Spinocerebellar ataxia type 3 ...... son disease in a black family.
@en
prefLabel
Spinocerebellar ataxia type 3 ...... son disease in a black family.
@ast
Spinocerebellar ataxia type 3 ...... son disease in a black family.
@en
P2093
P1433
P1476
Spinocerebellar ataxia type 3 ...... son disease in a black family.
@en
P2093
A Singleton
P Critchley
P O'Suilleabhain
P304
P356
10.1001/ARCHNEUR.58.2.296
P577
2001-02-01T00:00:00Z