International audienceObjective: This study was undertaken to identify magnetic resonance (MR) metrics that are most sensitive to early changes in the brain in spinocerebellar ataxia type 1 (SCA1) and type 3 (SCA3) using an advanced multimodal MR imaging (MRI) protocol in the multisite trial setting. Methods: SCA1 or SCA3 mutation carriers and controls (n = 107) underwent MR scanning in the US-European READISCA study to obtain structural, diffusion MRI, and MR spectroscopy data using an advanced protocol at 3T. Morphometric, microstructural, and neurochemical metrics were analyzed blinded to diagnosis and compared between preataxic SCA (n = 11 SCA1, n = 28 SCA3), ataxic SCA (n = 14 SCA1, n = 37 SCA3), and control (n = 17) groups using nonpa...
International audienceBackground and Objective: In spinocerebellar ataxia, ataxia onset can be prece...
<p>BACKGROUND: Spinocerebellar ataxias (SCAs) belong to the group of polyglutamine repeat disorders ...
OBJECTIVE: To identify factors that determine disease severity and clinical phenotype of the most c...
International audienceObjective: This study was undertaken to identify magnetic resonance (MR) metri...
Background: Given that new therapeutic options for spinocerebellar ataxias are on the horizon, there...
Background: All spinocerebellar ataxias (SCAs) are rare diseases. SCA1, 2, 3 and 6 are the four most...
Introduction: We aimed to uncover the pattern of network-level changes in neuronal function in Spino...
Background: The spinocerebellar ataxias (SCAs) are a group of autosomal dominant degenerative diseas...
Autosomal-dominant spinocerebellar ataxias (SCA) are neurodegenerative diseases characterized by pro...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Polyglutamine expansion spinocer...
Autosomal-dominant spinocerebellar ataxias (SCA) are neurodegenerative diseases characterized by pro...
Background: Spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disorder that affects the ce...
Background: Disease severity in spinocerebellar ataxia type 3 (SCA3) is commonly defined by the Scal...
Spinocerebellar ataxias are dominantly inherited disorders that are associated with progressive brai...
International audienceBackground and Objective: In spinocerebellar ataxia, ataxia onset can be prece...
<p>BACKGROUND: Spinocerebellar ataxias (SCAs) belong to the group of polyglutamine repeat disorders ...
OBJECTIVE: To identify factors that determine disease severity and clinical phenotype of the most c...
International audienceObjective: This study was undertaken to identify magnetic resonance (MR) metri...
Background: Given that new therapeutic options for spinocerebellar ataxias are on the horizon, there...
Background: All spinocerebellar ataxias (SCAs) are rare diseases. SCA1, 2, 3 and 6 are the four most...
Introduction: We aimed to uncover the pattern of network-level changes in neuronal function in Spino...
Background: The spinocerebellar ataxias (SCAs) are a group of autosomal dominant degenerative diseas...
Autosomal-dominant spinocerebellar ataxias (SCA) are neurodegenerative diseases characterized by pro...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Polyglutamine expansion spinocer...
Autosomal-dominant spinocerebellar ataxias (SCA) are neurodegenerative diseases characterized by pro...
Background: Spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disorder that affects the ce...
Background: Disease severity in spinocerebellar ataxia type 3 (SCA3) is commonly defined by the Scal...
Spinocerebellar ataxias are dominantly inherited disorders that are associated with progressive brai...
International audienceBackground and Objective: In spinocerebellar ataxia, ataxia onset can be prece...
<p>BACKGROUND: Spinocerebellar ataxias (SCAs) belong to the group of polyglutamine repeat disorders ...
OBJECTIVE: To identify factors that determine disease severity and clinical phenotype of the most c...