The aim of this study was to examine the different patterns of cerebellar and/or brainstem
atrophy in spinocerebellar ataxia (SCA) type 3 and 6. Eighteen patients (SCA3 n= 9, SCA6 …

Spinocerebellar ataxia type 7 (SCA7) is a progressive neurodegenerative disorder
characterized by cerebellar ataxia and visual loss. It is caused by a CAG repeat expansion …

Background and objective Neuropathological description of the brain in spinocerebellar
ataxia type 1 (SCA1) is limited to a few cases. Voxel-based morphometry (VBM) enables an …

BACKGROUND AND OBJECTIVE: Biomarkers to monitor neurological dysfunction in
autosomal dominant inherited spinocerebellar ataxias (SCA) are lacking. We therefore …

Abstract Spinocerebellar ataxia type 3 (SCA3) is the most frequent inherited cerebellar
ataxia in Europe, the US and Japan, leading to disability and death through motor …

INTRODUCTION: Spinocerebellar ataxias (SCA) are a group of autosomal dominant ataxias
with varied clinical phenotypes. However there are no unique distinguishing features on …

Background Spinocerebellar ataxia type 3 (SCA3) is a complex cerebrocerebellar disease
primarily characterized by ataxia symptoms alongside motor and cognitive impairments. The …

Abstract Spinocerebellar Ataxia Type 2 (SCA2) is a genetic disorder causing cerebellar
degeneration that result in motor and cognitive alterations. Voxel-based morphometry (VBM) …

Abstract Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant neurodegenerative
disease involving the cerebellum and characterized by a typical motor syndrome. In …

BACKGROUND AND PURPOSE: Cerebellar and brain stem atrophy are important features
in SCA3, whereas SCA6 has been regarded as a “pure” cerebellar disease. However …