Saccades in presymptomatic and early stages of Huntington disease

No abstract is available for this paper.

• Publication year

  2006

• Venue

  Neurology

• Publication date

  2006-08-08

• Fields of study

  Medicine, Psychology

• Identifiers
  DOI 10.1212/01.wnl.0000227890.87398.c1PMID 16855205
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Regional cortical thinning in preclinical Huntington disease and its relationship to cognition

  2005cited by this paper
• Oculomotor control in asymptomatic and recently diagnosed individuals with the genetic marker for Huntington's disease.

  2004cited by this paper
• Functional brain changes in presymptomatic Huntington's disease

  2004cited by this paper
• Onset and rate of striatal atrophy in preclinical Huntington disease

  2004cited by this paper
• fMRI biomarker of early neuronal dysfunction in presymptomatic Huntington's Disease.

  2004cited by this paper
• Clinical markers of early disease in persons near onset of Huntington’s disease

  2001cited by this paper
• Subtle changes among presymptomatic carriers of the Huntington's disease gene

  2000cited by this paper
• Nuclear and Neuropil Aggregates in Huntington’s Disease: Relationship to Neuropathology

  1999cited by this paper
• A preliminary study of acute responses to clamped alcohol concentration and family history of alcoholism.

  1999cited by this paper
• Age-related performance of human subjects on saccadic eye movement tasks

  1998cited by this paper
• Ocular motor abnormalities in Huntington's disease.

  1997cited by this paper
• Unified Huntington's disease rating scale: reliability and consistency

  1996cited by this paper
• Direct amplification of the CAG repeat of huntingtin without amplification of CCG.

  1996cited by this paper
• Motor changes in presymptomatic Huntington disease gene carriers.

  1996cited by this paper
• Striatal D1 and D2 dopamine receptor loss in asymptomatic mutation carriers of Huntington's disease

  1996cited by this paper
• Unified Huntington's disease rating scale: Reliability and consistency

  1996cited by this paper
• Human oculomotor function: reliability and diurnal variation.

  1995cited by this paper
• Automobile driving in Huntington's disease

  1995cited by this paper
• A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group.

  1993cited by this paper
• Unimpaired verbal memory and oculomotor control in asymptomatic adults with the genetic marker for Huntington's disease.

  1993cited by this paper
• A non-organic and non-enzymatic extraction method gives higher yields of genomic DNA from whole-blood samples than do nine other methods tested.

  1992cited by this paper
• Saccades in Huntington's disease

  1991cited by this paper
• Oculomotor defects in patients with Huntington's disease and their offspring.

  1988cited by this paper
• Saccades in Huntington's disease

  1987cited by this paper
• Dynamic modification of the vestibulo-ocular reflex by the nodulus and uvula.

  1985cited by this paper
• The Neurology of Eye Movements

  1984cited by this paper
• Abnormal ocular motor control in Huntington's disease

  1983cited by this paper
• The main sequence, a tool for studying human eye movements

  1975cited by this paper
• A disorder of rapid eye movements in Huntington's chorea.

  1967cited by this paper

• Eye manifestations in Huntington’s disease: an update on the potential of ocular biomarkers

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• Digital health in presymptomatic diseases.

  2025cites this paper
• Repeatability, reliability, and stability of eye movement measurements in Parkinson’s disease, cerebellar ataxia, and healthy adults

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• The Newborn Screening Programme Revisited: An Expert Opinion on the Challenges of Rett Syndrome

  2024cites this paper
• The antisaccadic paradigm: A complementary neuropsychological tool in basal ganglia disorders.

  2024cites this paper
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  2023cites this paper
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  2022cites this paper
• Digital Phenotyping in Clinical Neurology

  2022cites this paper
• Evolution of eye movement abnormalities in Huntington’s disease

  2022cites this paper
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  2020cites this paper
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  2019cites this paper
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  2019cites this paper
• Ocular motor manifestations of movement disorders.

  2019cites this paper
• The effect of impulsivity and inhibitory control deficits in the saccadic behavior of premanifest Huntington’s disease individuals

  2019cites this paper
• Discriminating between anticipatory and visually triggered saccades: measuring minimal visual saccadic response time using luminance.

  2019cites this paper
• Eye Movement Disorders

  2019cites this paper
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  2019cites this paper
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  2019cites this paper
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  2018cites this paper
• Neuro-ophthalmologic assessment and investigations in children and adults with cerebellar diseases.

  2018cites this paper
• The Relationship between Saccades and Locomotion

  2018cites this paper
• Compensation Related Utilization of Neural Circuits Hypothesis Model in Response Inhibition in Premanifest Huntington’s Disease

  2018cites this paper
• Vergence and Strabismus in Neurodegenerative Disorders

  2018cites this paper
• Cognitive and behavioral changes in Huntington disease before diagnosis.

  2017cites this paper
• Basic and translational neuro-ophthalmology of visually guided saccades: disorders of velocity

  2017cites this paper
• Rôle de la huntingtine dans le muscle

  2017cites this paper
• Preclinical motor manifestations of Huntington disease.

  2017cites this paper
• Analyse des mouvements oculaires saccadiques à la phase prodromale de la maladie d’Alzheimer

  2017cites this paper
• Optical Coherence Tomography in Neurodegenerative Disorders

  2016cites this paper
• Abnormal eye movements in three types of chorea

  2016cites this paper
• The impact of oculomotor functioning on neuropsychological performance in Huntington disease

  2016cites this paper
• Loss of extra-striatal phosphodiesterase 10A expression in early premanifest Huntington's disease gene carriers.

  2016cites this paper
• Clinical-Genetic Associations in the Prospective Huntington at Risk Observational Study (PHAROS): Implications for Clinical Trials.

  2016cites this paper
• The Corticospinal Tract in Huntington's Disease.

  2015cites this paper
• Optical coherence tomography findings in Huntington’s disease: a potential biomarker of disease progression

  2015cites this paper
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  2015cites this paper
• Spontaneous improvement in oculomotor function of children with cerebral palsy.

  2015cites this paper
• Classification of Huntington’s disease stage with support vector machines: A study on oculomotor performance

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• Ocular motor abnormalities in neurodegenerative disorders

  2015cites this paper
• The diagnostic value of saccades in movement disorder patients: a practical guide and review

  2015cites this paper
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  2015cites this paper
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  2015cites this paper
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  2014cites this paper
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  2014cites this paper
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  2014cites this paper
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  2014cites this paper
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  2013cites this paper
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  2013cites this paper
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  2013cites this paper
• Antisaccade task reflects cortical involvement in mild cognitive impairment

  2013cites this paper
• Autoimmune chorea in adults

  2013cites this paper
• Multicenter validation of a bedside antisaccade task as a measure of executive function

  2012cites this paper
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  2012cites this paper
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  2012cites this paper
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  2011cites this paper
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  2011cites this paper
• Clinical impairment in premanifest and early Huntington's disease is associated with regionally specific atrophy

  2011cites this paper
• Disorders of higher gaze control.

  2011cites this paper
• Longitudinal Change in Gait and Motor Function in Pre-manifest Huntington’s Disease

  2011cites this paper
• Huntington's disease: from molecular pathogenesis to clinical treatment

  2011cites this paper
• Preclinical assessment of CNS drug action using eye movements in mice.

  2011cites this paper
• Re fl exive and volitional saccades : Biomarkers of Huntington disease severity and progression

  2011cites this paper
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  2011cites this paper
• Abnormal error-related antisaccade activation in premanifest and early manifest Huntington disease.

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• Assessment of motor symptoms and functional impact in prodromal and early huntington disease.

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  2011cites this paper
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• NEURAL CORRELATES AND PROGRESSION OF SACCADE IMPAIRMENT IN PREMANIFEST AND MANIFEST HUNTINGTON DISEASE

  2010cites this paper
• Huntington disease

  2010cites this paper
• Early Detection of Huntington Disease.

  2010cites this paper
• Huntington’s disease: changes in saccades and hand-tapping over 3 years

  2010cites this paper
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