Background: Given that new therapeutic options for spinocerebellar ataxias are on the horizon, there is a need for markers that reflect disease-related alterations, in particular, in the preataxic stage, in which clinical scales are lacking sensitivity. Objective: The objective of this study was to quantify regional brain volumes and upper cervical spinal cord areas in spinocerebellar ataxia type 3 in vivo across the entire time course of the disease. Methods: We applied a brain segmentation approach that included a lobular subsegmentation of the cerebellum to magnetic resonance images of 210 ataxic and 48 preataxic spinocerebellar ataxia type 3 mutation carriers and 63 healthy controls. In addition, cervical cord cross-sectional areas were...
BACKGROUND AND OBJECTIVE: Biomarkers to monitor neurological dysfunction in autosomal dominant inher...
ObjectiveSpinocerebellar ataxia type 2 (SCA2) is an autosomal dominantly inherited neurodegenerative...
BACKGROUND: Clinical trials in SCA3 will require biomarkers for use as outcome measures. METHODS: To...
Background Given that new therapeutic options for spinocerebellar ataxias are on the horizon, there ...
Background: Disease severity in spinocerebellar ataxia type 3 (SCA3) is commonly defined by the Scal...
Background and objective: Spinocerebellar ataxia 7 (SCA7) is characterised by cerebellar ataxia and ...
International audienceObjective: This study was undertaken to identify magnetic resonance (MR) metri...
Background: The spinocerebellar ataxias (SCAs) are a group of autosomal dominant degenerative diseas...
Introduction: We aimed to uncover the pattern of network-level changes in neuronal function in Spino...
Objective: Friedreich ataxia (FRDA) is an inherited neurological disease defined by progressive move...
Background Spinocerebellar ataxia type 3 is a rare neurodegenerative disease caused by a CAG repeat ...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Polyglutamine expansion spinocer...
BACKGROUND AND OBJECTIVE: Biomarkers to monitor neurological dysfunction in autosomal dominant inher...
ObjectiveSpinocerebellar ataxia type 2 (SCA2) is an autosomal dominantly inherited neurodegenerative...
BACKGROUND: Clinical trials in SCA3 will require biomarkers for use as outcome measures. METHODS: To...
Background Given that new therapeutic options for spinocerebellar ataxias are on the horizon, there ...
Background: Disease severity in spinocerebellar ataxia type 3 (SCA3) is commonly defined by the Scal...
Background and objective: Spinocerebellar ataxia 7 (SCA7) is characterised by cerebellar ataxia and ...
International audienceObjective: This study was undertaken to identify magnetic resonance (MR) metri...
Background: The spinocerebellar ataxias (SCAs) are a group of autosomal dominant degenerative diseas...
Introduction: We aimed to uncover the pattern of network-level changes in neuronal function in Spino...
Objective: Friedreich ataxia (FRDA) is an inherited neurological disease defined by progressive move...
Background Spinocerebellar ataxia type 3 is a rare neurodegenerative disease caused by a CAG repeat ...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Polyglutamine expansion spinocer...
BACKGROUND AND OBJECTIVE: Biomarkers to monitor neurological dysfunction in autosomal dominant inher...
ObjectiveSpinocerebellar ataxia type 2 (SCA2) is an autosomal dominantly inherited neurodegenerative...
BACKGROUND: Clinical trials in SCA3 will require biomarkers for use as outcome measures. METHODS: To...