Objective: A sensorimotor network structural phenotype predicted motor task performance in a previous study in Huntington's disease (HD) gene carriers. We investigated in the visual network whether structure - function - behaviour relationship patterns, and the effects of the HD mutation, extended beyond the sensorimotor network. Methods: We used multimodal visual network MRI structural measures (cortical thickness and white matter connectivity), plus visual evoked potentials and task performance (Map Search; Symbol Digit Modalities Test) in healthy controls and HD gene carriers. Results: Using principal component (PC) analysis, we identified a structure - function relationship common to both groups. PC scores differed between groups indica...
Huntington's disease (HD) is a genetically caused neurodegenerative disorder characterized by hetero...
Background: Functional neural impairments have been documented in people with symptomatic Huntington...
Huntington’s disease (HD) is a genetically caused neurodegenerative disorder characterized by hetero...
Objective: A sensorimotor network structural phenotype predicted motor task performance in a previou...
Huntington's disease (HD) is an autosomal‐dominant inherited neurodegenerative disorder characterize...
Objectives: To investigate the function-structure relationship of white matter within different stag...
OBJECTIVES: To investigate the function-structure relationship of white matter within different stag...
International audienceHuntington's disease (HD) is a monogenic neurodegenerative disorder caused by ...
Objective: To investigate structural connectivity and the relationship between axonal microstructure...
Huntington's disease is an incurable neurodegenerative disease caused by inheritance of an expanded ...
International audienceResting‐state functional magnetic resonance imaging (rs‐fMRI) has the potentia...
Background: Huntington's disease is a neurodegenerative disorder characterized by clinical alteratio...
While the HTT CAG-repeat expansion mutation causing Huntington's disease (HD) is highly correlated w...
Huntington's disease is an incurable neurodegenerative disease caused by inheritance of an expanded ...
Subtle changes in motor function have been observed in individuals with prodromal Huntington disease...
Huntington's disease (HD) is a genetically caused neurodegenerative disorder characterized by hetero...
Background: Functional neural impairments have been documented in people with symptomatic Huntington...
Huntington’s disease (HD) is a genetically caused neurodegenerative disorder characterized by hetero...
Objective: A sensorimotor network structural phenotype predicted motor task performance in a previou...
Huntington's disease (HD) is an autosomal‐dominant inherited neurodegenerative disorder characterize...
Objectives: To investigate the function-structure relationship of white matter within different stag...
OBJECTIVES: To investigate the function-structure relationship of white matter within different stag...
International audienceHuntington's disease (HD) is a monogenic neurodegenerative disorder caused by ...
Objective: To investigate structural connectivity and the relationship between axonal microstructure...
Huntington's disease is an incurable neurodegenerative disease caused by inheritance of an expanded ...
International audienceResting‐state functional magnetic resonance imaging (rs‐fMRI) has the potentia...
Background: Huntington's disease is a neurodegenerative disorder characterized by clinical alteratio...
While the HTT CAG-repeat expansion mutation causing Huntington's disease (HD) is highly correlated w...
Huntington's disease is an incurable neurodegenerative disease caused by inheritance of an expanded ...
Subtle changes in motor function have been observed in individuals with prodromal Huntington disease...
Huntington's disease (HD) is a genetically caused neurodegenerative disorder characterized by hetero...
Background: Functional neural impairments have been documented in people with symptomatic Huntington...
Huntington’s disease (HD) is a genetically caused neurodegenerative disorder characterized by hetero...