about
Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study.SCA8 should not be tested in isolation for ataxia.Genetic analysis of age at onset variation in spinocerebellar ataxia type 2.Past, present and future therapeutics for cerebellar ataxias.Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.PTPRR protein tyrosine phosphatase isoforms and locomotion of vesicles and mice.Perceptual and acoustic analysis of speech in individuals with spinocerebellar ataxia (SCA).ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxiaAn approach to the patient with late-onset cerebellar ataxia.Cerebellar cognitive affective syndrome and autosomal recessive spastic ataxia of charlevoix-saguenay: a report of two male sibs.Assessment of whole-brain white matter by DTI in autosomal recessive spastic ataxia of Charlevoix-Saguenay.Spinocerebellar ataxia: a rational approach to aetiological diagnosis.Ramsay Hunt syndrome: clinical characterization of progressive myoclonus ataxia caused by GOSR2 mutation.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Recent advances in hereditary spinocerebellar ataxias.
@ast
Recent advances in hereditary spinocerebellar ataxias.
@en
type
label
Recent advances in hereditary spinocerebellar ataxias.
@ast
Recent advances in hereditary spinocerebellar ataxias.
@en
prefLabel
Recent advances in hereditary spinocerebellar ataxias.
@ast
Recent advances in hereditary spinocerebellar ataxias.
@en
P2093
P2860
P356
P1476
Recent advances in hereditary spinocerebellar ataxias.
@en
P2093
Bart P C van de Warrenburg
Berry Kremer
Richard J Sinke
P2860
P304
P356
10.1093/JNEN/64.3.171
P577
2005-03-01T00:00:00Z