Spinocerebellar Ataxias in Brazil—Frequencies and Modulating Effects of Related Genes

Factors Influencing Disease Progression in Autosomal Dominant Cerebellar Ataxia and Spastic Paraplegia

(2012) Perrine Charles   ARCHIVES OF NEUROLOGY

‘Costa da Morte’ ataxia is spinocerebellar ataxia 36: clinical and genetic characterization

(2012) María García-Murias et al.   BRAIN

Spinocerebellar ataxias – genotype-phenotype correlations in 104 Brazilian families

(2012) HA Teive et al.   Clinics

Expansion of Intronic GGCCTG Hexanucleotide Repeat in NOP56 Causes SCA36, a Type of Spinocerebellar Ataxia Accompanied by Motor Neuron Involvement

(2011) Hatasu Kobayashi et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The APOE ε2 Allele Increases the Risk of Earlier Age at Onset in Machado-Joseph Disease

(2011) Conceição Bettencourt   ARCHIVES OF NEUROLOGY

The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: A 2-year follow-up study

(2011) H. Jacobi et al.   NEUROLOGY

Spinocerebellar ataxia type 10 – A review

(2011) Hélio A.G. Teive et al.   PARKINSONISM & RELATED DISORDERS

The Genomic Ancestry of Individuals from Different Geographical Regions of Brazil Is More Uniform Than Expected

(2011) Sérgio D. J. Pena et al.   PLoS One

Progression Rate of Neurological Deficits in a 10-Year Cohort of SCA3 Patients

(2010) Laura Bannach Jardim et al.   CEREBELLUM

Does DNA methylation in the promoter region of the ATXN3 gene modify age at onset in MJD (SCA3) patients?

(2010) VE Emmel et al.   CLINICAL GENETICS

Spinocerebellar ataxia type 10: Frequency of epilepsy in a large sample of Brazilian patients

(2010) Hélio A.G. Teive et al.   MOVEMENT DISORDERS

Spinocerebellar Ataxia Type 31 Is Associated with “Inserted” Penta-Nucleotide Repeats Containing (TGGAA)n

(2009) Nozomu Sato et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal

(2009) J. Vale et al.   EUROPEAN JOURNAL OF NEUROLOGY

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

(2009) Teresa Almeida et al.   PLoS One

Spinocerebellar ataxia types 1, 2, 3, and 6: Disease severity and nonataxia symptoms

(2008) T. Schmitz-Hubsch et al.   NEUROLOGY

Intrafamilial variability of Parkinson phenotype in SCAs: Novel cases due to SCA2 and SCA3 expansions

(2008) M.P. Socal et al.   PARKINSONISM & RELATED DISORDERS

Polyglutamine Genes Interact to Modulate the Severity and Progression of Neurodegeneration in Drosophila

(2008) Derek Lessing et al.   PLOS BIOLOGY