Analysis of SCA8, SCA10, SCA12, SCA17 and SCA19 in patients with unknown spinocerebellar ataxia: a Thai multicentre study

Clinical analysis of adult-onset spinocerebellar ataxias in Thailand

(2014) Pairoj Boonkongchuen et al.   BMC Neurology

SCA 17 phenotype with intermediate triplet repeat number

(2014) Heather Herrema et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Glucocerebrosidase mutations in Thai patients with Parkinson's disease

(2014) Teeratorn Pulkes et al.   PARKINSONISM & RELATED DISORDERS

Mutations in potassium channelkcnd3cause spinocerebellar ataxia type 19

(2012) Anna Duarri et al.   ANNALS OF NEUROLOGY

Mutations inKCND3cause spinocerebellar ataxia type 22

(2012) Yi-Chung Lee et al.   ANNALS OF NEUROLOGY

Milestones in ataxia

(2011) Thomas Klockgether et al.   MOVEMENT DISORDERS

Spinocerebellar ataxia type 17 mutation as a causative and susceptibility gene in parkinsonism

(2009) J-Y Kim et al.   NEUROLOGY

Ancestral Origin of the ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10 (SCA10)

(2009) Teresa Almeida et al.   PLoS One