Impaired saccadic adaptation in DYT11 dystonia

No abstract is available for this paper.

• Publication year

  2011

• Venue

  Journal of Neurology Neurosurgery & Psychiatry

• Publication date

  2011-03-08

• Fields of study

  Medicine

• Identifiers
  DOI 10.1136/jnnp.2010.232793PMID 21386109
• 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.

• SGCE isoform characterization and expression in human brain: implications for myoclonus–dystonia pathogenesis?

  2011cited by this paper
• Disruption of Saccadic Adaptation with Repetitive Transcranial Magnetic Stimulation of the Posterior Cerebellum in Humans

  2010cited by this paper
• Myoclonus-dystonia and spinocerebellar ataxia type 14 presenting with similar phenotypes: trunk tremor, myoclonus, and dystonia.

  2010cited by this paper
• Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond.

  2010cited by this paper
• Disorganized sensorimotor integration in mutation-positive myoclonus-dystonia: a functional magnetic resonance imaging study.

  2010cited by this paper
• Cerebellum Can Be a Possible Generator of Progressive Myoclonus

  2010cited by this paper
• Sensorimotor adaptation of saccadic eye movements.

  2010cited by this paper
• Myoclonus‐dystonia: An update

  2009cited by this paper
• Pathophysiology of dystonia

  2009cited by this paper
• Impaired sensorimotor integration in focal hand dystonia patients in the absence of symptoms

  2009cited by this paper
• Cerebellothalamocortical Connectivity Regulates Penetrance in Dystonia

  2009cited by this paper
• Myoclonus–dystonia

  2008cited by this paper
• Electrophysiological features of myoclonus‐dystonia

  2008cited by this paper
• A neurophysiological study of myoclonus in patients with DYT11 myoclonus‐dystonia syndrome

  2008cited by this paper
• Neurophysiological evidence for cerebellar dysfunction in primary focal dystonia

  2008cited by this paper
• Increased cerebellar activation during sequence learning in DYT1 carriers: an equiperformance study.

  2007cited by this paper
• Structural abnormalities in the cerebellum and sensorimotor circuit in writer's cramp

  2007cited by this paper
• Activity in the Lateral Intraparietal Area Predicts the Goal and Latency of Saccades in a Free-Viewing Visual Search Task

  2006cited by this paper
• Pathophysiology of dystonia.

  2006cited by this paper
• Animal models of generalized dystonia

  2005cited by this paper
• Progressive myoclonus in a child with a deep cerebellar mass

  2004cited by this paper
• Progressive myoclonus in a child with a deep cerebellar mass

  2003cited by this paper
• “Motor circuit” gray matter changes in idiopathic cervical dystonia

  2003cited by this paper
• Involvement of the cerebellar thalamus in human saccade adaptation

  2001cited by this paper
• Modulation of saccadic eye movements by predicted reward outcome

  2001cited by this paper
• Clinical characteristics and topography of lesions in movement disorders due to thalamic lesions

  2001cited by this paper
• Cerebellar lesions impair rapid saccade amplitude adaptation

  2001cited by this paper
• Irregular jerky tremor, myoclonus, and thalamus: A study using low‐frequency stimulation

  2000cited by this paper
• Neurology of saccades and smooth pursuit.

  1999cited by this paper
• Parametric adjustment in saccadic eye movements

  1967cited by this paper

• Convergence Deficits in Myoclonus-Dystonia Point to Cerebellar Impairment.

  2026cites this paper
• Divergent Cerebello-Cortical Network Responses to Emotional Stress in Myoclonus Dystonia.

  2026cites this paper
• Cerebellar contributions to dystonia: unraveling the role of Purkinje cells and cerebellar nuclei

  2025cites this paper
• From SGCE gene to symptoms: decoding myoclonus-dystonia.

  2025cites this paper
• Sex-specific alterations of Purkinje cell firing in Sgce knockout mice and correlations with myoclonus.

  2025cites this paper
• Reflexive and voluntary saccades as a proxy for bradykinesia and apathy in Parkinson’s disease

  2025cites this paper
• Association of abnormal explicit sense of agency with cerebellar impairment in myoclonus-dystonia

  2024cites this paper
• Psychiatric phenotype in neurodevelopmental myoclonus-dystonia is underpinned by abnormality of cerebellar modulation on the cerebral cortex

  2024cites this paper
• Pallidal deep brain stimulation for patients with myoclonus-dystonia without SGCE mutations

  2024cites this paper
• ε-sarcoglycan myoclonus-dystonia—overview of neurophysiological, behavioral, and imaging characteristics

  2024cites this paper
• Cerebellar Dysfunction as a Source of Dystonic Phenotypes in Mice

  2022cites this paper
• Synaptic effects of ethanol on striatal circuitry: therapeutic implications for dystonia

  2021cites this paper
• ε-Sarcoglycan: Unraveling the Myoclonus-Dystonia Gene

  2021cites this paper
• Impaired Saccade Adaptation in Tremor-Dominant Cervical Dystonia—Evidence for Maladaptive Cerebellum

  2020cites this paper
• Visual Sensory Processing is Altered in Myoclonus Dystonia

  2020cites this paper
• Early Onset Ataxia with Comorbid Dystonia: Clinical, Anatomical and Biological Pathway Analysis Expose Shared Pathophysiology

  2020cites this paper
• Olfaction as a Marker for Dystonia: Background, Current State and Directions

  2020cites this paper
• Dissociation in reactive and proactive inhibitory control in Myoclonus dystonia

  2020cites this paper
• Twenty years on: Myoclonus‐dystonia and ε‐sarcoglycan — neurodevelopment, channel, and signaling dysfunction

  2019cites this paper
• Sensorimotor Control in Dystonia

  2019cites this paper
• Étude du sens d'agentivité dans la dystonie myoclonique

  2019cites this paper
• Delineating cerebellar mechanisms in DYT11 myoclonus‐dystonia

  2018influential citation
• Adaptation of feedforward movement control is abnormal in patients with cervical dystonia and tremor.

  2018cites this paper
• Partial loss‐of‐function of sodium channel SCN8A in familial isolated myoclonus

  2018cites this paper
• Myoclonus-dystonia: classification, phenomenology, pathogenesis, and treatment

  2018cites this paper
• University of Birmingham Delineating cerebellar mechanisms in DYT11 myoclonus-dystonia

  2018cites this paper
• The Anatomical Basis for Dystonia: The Motor Network Model

  2017cites this paper
• Abnormalities of Eye–Hand Coordination in Patients with Writer’s Cramp: Possible Role of the Cerebellum

  2017cites this paper
• Chapter 11 – Dystonia

  2016cites this paper
• Improvement of Isolated Myoclonus Phenotype in Myoclonus Dystonia after Pallidal Deep Brain Stimulation

  2016cites this paper
• To jerk or not to jerk: A clinical pathophysiology of myoclonus.

  2016cites this paper
• Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia

  2016cites this paper
• The role of the cerebellum in the pathophysiology of dystonia

  2016cites this paper
• Chapter 28 – Rodent Models of Autosomal Dominant Primary Dystonia

  2015cites this paper
• RELN rare variants in myoclonus‐dystonia

  2015cites this paper
• Genetic architecture of dystonia

  2014cites this paper
• Habilitationsschrift Functional Imaging in Hereditary Dystonia

  2014cites this paper
• The neurophysiological features of myoclonus-dystonia and differentiation from other dystonias.

  2014cites this paper
• Dystonia as a network disorder: what is the role of the cerebellum?

  2014influential citation
• Adaptation of naturally paced saccades.

  2014cites this paper
• Metabolic changes in DYT11 myoclonus-dystonia

  2013cites this paper
• Defective cerebellar control of cortical plasticity in writer's cramp.

  2013cites this paper
• The anatomical basis of dystonia: Current view using neuroimaging

  2013cites this paper
• Engineering animal models of dystonia

  2013cites this paper
• Recent Advances in the Molecular Pathogenesis of Dystonia-Plus Syndromes and Heredodegenerative Dystonias

  2013cites this paper
• Functional MRI study of response inhibition in myoclonus dystonia.

  2013cites this paper
• SGCE mutations cause psychiatric disorders: clinical and genetic characterization.

  2013cites this paper
• Identification, Validation and Characterization of the Mutation on Chromosome 18p which is Responsible for Causing Myoclonus-Dystonia

  2012cites this paper
• Tremor-spectrum in spinocerebellar ataxia type 3

  2012cites this paper
• UvA-DARE ( Digital Academic Repository ) Phenotypes and mechanisms in myoclonus-dystonia

  2012cites this paper
• Abnormal nuclear envelope in the cerebellar Purkinje cells and impaired motor learning in DYT11 myoclonus-dystonia mouse models.

  2012cites this paper
• Cecilia BonnetEmmanuelle ApartisMathieu Anheim • Andre P. LegrandJose F. Baizabal-Carvallo • Anne M. BonnetAlexandra DurrMarie Vidailhet

  2012cites this paper
• Les nouvelles approches des dystonies (clinique, génétique et hypothèses physio-pathologiques)

  2011cites this paper
• Myoclonus-dystonia : a cerebellar disorder ? Myoclonus-dystonia : a synaptopathy ? Myoclonus-dystonia :

  year unknowncites this paper
• Sex-speci fi c alterations of Purkinje cell fi ring in Sgce knockout mice and correlations with myoclonus

  year unknowncites this paper