The authors examined oculomotor function to identify a biomarker of disease progression in genetically confirmed preclinical and early clinical Huntington disease (HD). Initiation deficits of voluntary-guided, but not reflexive, saccades were characteristic of preclinical HD. Saccadic slowing and delayed reflexive saccades were demonstrated in clinical but not preclinical HD. Saccadic measures provide biomarkers of disease progression in both preclinical and early clinical stages of HD. Copyright © 2006 by AAN Enterprises, Inc
Huntington disease (HD) can be seen as a model neurodegenerative disorder, in that it is caused by a...
Indiana University-Purdue University Indianapolis (IUPUI)Huntington disease (HD) is an autosomal dom...
Huntington's chorea is a chronic, progressive, fatal, degenerative disorder of the central nervous s...
Huntington’s disease (HD), a genetically inherited neurodegenerative disease caused by CAG trinucleo...
We review here the eye movements in patients with Huntington's disease (HD), concentrating upon sacc...
Huntingtons disease produces disturbances of voluntary gaze, particularly saccades. It is caused by ...
Huntingtons disease produces disturbances of voluntary gaze, particularly saccades. It is caused by ...
We review here the eye movements in patients with Huntington's disease (HD), concentrating upon sacc...
AbstractWe compared oculomotor control among individuals in the early stages of Huntington’s disease...
<div><p>Introduction</p><p>Different oculomotor abnormalities have been reported to occur in premani...
AbstractWe compared oculomotor control among individuals in the early stages of Huntington’s disease...
This study examined two possible genetic markers of Huntington's chorea: eye movements and electrode...
This study examined two possible genetic markers of Huntington's chorea: eye movements and electrode...
Abstract Eye movement abnormalities can be distinctive and suggestive of a specific pathophysiology....
Background and purpose: Huntington disease (HD) is a neurodegenerative disease leading to involunta...
Huntington disease (HD) can be seen as a model neurodegenerative disorder, in that it is caused by a...
Indiana University-Purdue University Indianapolis (IUPUI)Huntington disease (HD) is an autosomal dom...
Huntington's chorea is a chronic, progressive, fatal, degenerative disorder of the central nervous s...
Huntington’s disease (HD), a genetically inherited neurodegenerative disease caused by CAG trinucleo...
We review here the eye movements in patients with Huntington's disease (HD), concentrating upon sacc...
Huntingtons disease produces disturbances of voluntary gaze, particularly saccades. It is caused by ...
Huntingtons disease produces disturbances of voluntary gaze, particularly saccades. It is caused by ...
We review here the eye movements in patients with Huntington's disease (HD), concentrating upon sacc...
AbstractWe compared oculomotor control among individuals in the early stages of Huntington’s disease...
<div><p>Introduction</p><p>Different oculomotor abnormalities have been reported to occur in premani...
AbstractWe compared oculomotor control among individuals in the early stages of Huntington’s disease...
This study examined two possible genetic markers of Huntington's chorea: eye movements and electrode...
This study examined two possible genetic markers of Huntington's chorea: eye movements and electrode...
Abstract Eye movement abnormalities can be distinctive and suggestive of a specific pathophysiology....
Background and purpose: Huntington disease (HD) is a neurodegenerative disease leading to involunta...
Huntington disease (HD) can be seen as a model neurodegenerative disorder, in that it is caused by a...
Indiana University-Purdue University Indianapolis (IUPUI)Huntington disease (HD) is an autosomal dom...
Huntington's chorea is a chronic, progressive, fatal, degenerative disorder of the central nervous s...