Background: Hunting-ton's disease (HD) is generally considered a hyperkinetic disorder, although hypokinetic features are part of the motor syndrome. Moreover, the striatum is considered to play a key role in initiating and executing motor programs and achieving optimal scheduling in response generation. Controversial results regarding the association between clinical features and markers of progression of the disease might be the result of inadequate restriction of clinical signs to the choreatic syndrome. Objective: To determine the relationship of neurologic motor and cognitive indices in patients with HD with intrinsic neuronal loss in the striatum, as measured using raclopride C11 and PET. Patients and Methods: A cross-sectional study ...
Huntington Disease (HD) is an autosomal-dominant, neurodegenerative disorder, including motor, cogni...
We used (11)C-raclopride PET, a marker of D(2) dopamine receptor binding, and statistical parametric...
Huntington's disease (HD) is an inherited autosomal dominant neurodegenerative disorder. The most pr...
Background: Hunting-ton's disease (HD) is generally considered a hyperkinetic disorder, although hyp...
The clinical diagnosis of Huntington's disease (HD) is based on the motor symptoms, although these c...
We have studied the progression of striatal and extrastriatal post-synaptic dopaminergic changes in ...
Seventeen individuals at risk for Huntington's disease and five symptomatic patients, who had previo...
The objective of this study is to investigate the progression of predominantly choreatic and hypokin...
IMPORTANCE: Brain hypometabolism is associated with the clinical consequences of the degenerative pr...
BACKGROUND: Understanding the relation between predominantly choreatic and hypokinetic-rigid motor s...
This article reviews the neurophysiological abnormalities described in Huntington's disease. Among t...
Besides chorea, hypokinesia is an important motor disturbance in Huntington's disease (HD) but its c...
The PREDICT-HD study seeks to identify clinical and biological markers of Huntington's disease in pr...
International audienceImportance: Brain hypometabolism is associated with the clinical consequences ...
The performance of 54 subjects genetically at risk for Huntington's disease was examined in double-b...
Huntington Disease (HD) is an autosomal-dominant, neurodegenerative disorder, including motor, cogni...
We used (11)C-raclopride PET, a marker of D(2) dopamine receptor binding, and statistical parametric...
Huntington's disease (HD) is an inherited autosomal dominant neurodegenerative disorder. The most pr...
Background: Hunting-ton's disease (HD) is generally considered a hyperkinetic disorder, although hyp...
The clinical diagnosis of Huntington's disease (HD) is based on the motor symptoms, although these c...
We have studied the progression of striatal and extrastriatal post-synaptic dopaminergic changes in ...
Seventeen individuals at risk for Huntington's disease and five symptomatic patients, who had previo...
The objective of this study is to investigate the progression of predominantly choreatic and hypokin...
IMPORTANCE: Brain hypometabolism is associated with the clinical consequences of the degenerative pr...
BACKGROUND: Understanding the relation between predominantly choreatic and hypokinetic-rigid motor s...
This article reviews the neurophysiological abnormalities described in Huntington's disease. Among t...
Besides chorea, hypokinesia is an important motor disturbance in Huntington's disease (HD) but its c...
The PREDICT-HD study seeks to identify clinical and biological markers of Huntington's disease in pr...
International audienceImportance: Brain hypometabolism is associated with the clinical consequences ...
The performance of 54 subjects genetically at risk for Huntington's disease was examined in double-b...
Huntington Disease (HD) is an autosomal-dominant, neurodegenerative disorder, including motor, cogni...
We used (11)C-raclopride PET, a marker of D(2) dopamine receptor binding, and statistical parametric...
Huntington's disease (HD) is an inherited autosomal dominant neurodegenerative disorder. The most pr...