Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds
about
Treatment for dysphagia (swallowing difficulties) in hereditary ataxiaGenetic neurological channelopathies: molecular genetics and clinical phenotypes.'Medusa head ataxia': the expanding spectrum of Purkinje cell antibodies in autoimmune cerebellar ataxia. Part 2: Anti-PKC-gamma, anti-GluR-delta2, anti-Ca/ARHGAP26 and anti-VGCCDistinct critical cerebellar subregions for components of verbal working memory.Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.The molecular biology of the autosomal-dominant cerebellar ataxias.Brain pathology of spinocerebellar ataxias.Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics.Clinical analysis of adult-onset spinocerebellar ataxias in Thailand.The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study.Early Cerebellar Network Shifting in Spinocerebellar Ataxia Type 6.Consensus paper: radiological biomarkers of cerebellar diseasesPredictive modeling by the cerebellum improves proprioception.Spinocerebellar ataxia type 6 in eastern India: Some new observations.Determination of Genotypic and Phenotypic Characteristics of Friedreich's Ataxia and Autosomal Dominant Spinocerebellar Ataxia Types 1, 2, 3, and 6Movement disorders in spinocerebellar ataxias."Atypical" atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-a diagnostic guide.An update on the cerebellar subtype of multiple system atrophy.Fragile X-associated tremor/ataxia syndrome: phenotypic comparisons with other movement disorders.Cognitive Changes in the Spinocerebellar Ataxias Due to Expanded Polyglutamine Tracts: A Survey of the Literature.Nucleation of protein aggregation kinetics as a basis for genotype-phenotype correlations in polyglutamine diseases.A patient homozygous for the SCA6 gene with retinitis pigmentosa.The aetiology of sporadic adult-onset ataxia.Differences in dysphagia between spinocerebellar ataxia type 3 and type 6.Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6.Evaluation of parkinsonism and striatal dopamine transporter loss in patients with spinocerebellar ataxia type 6.Peripheral Neuropathy in Spinocerebellar Ataxia Type 1, 2, 3, and 6.Spinocerebellar ataxia types 1, 2, 3 and 6: the clinical spectrum of ataxia and morphometric brainstem and cerebellar findings.Progression of Dysphagia in Spinocerebellar Ataxia Type 6.
P2860
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P2860
Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
@zh
1998年學術文章
@zh-hant
name
Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds
@ast
Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds
@en
type
label
Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds
@ast
Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds
@en
prefLabel
Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds
@ast
Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds
@en
P2093
P2860
P356
P1476
Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds
@en
P2093
P2860
P356
10.1136/JNNP.64.1.67
P407
P577
1998-01-01T00:00:00Z