Paroxysmal dyskinesias in mice

No abstract is available for this paper.

• Publication year

  2008

• Venue

  Movement Disorders

• Publication date

  2008-01-30

• Fields of study

  Biology, Medicine, Psychology

• Identifiers
  DOI 10.1002/mds.21829PMID 17999434PMCID PMC2887756
• 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.

• The paroxysmal dyskinesias

  2009cited by this paper
• Motor and cognitive deficits in the heterozygous leaner mouse, a Cav2.1 voltage-gated Ca2+ channel mutant.

  2008cited by this paper
• The ataxic groggy rat has a missense mutation in the P/Q-type voltage-gated Ca2+ channel alpha1A subunit gene and exhibits absence seizures.

  2007cited by this paper
• The ataxic groggy rat has a missense mutation in the P/Q-type voltage-gated Ca[2+] channel α1A subunit gene and exhibits absence seizures

  2007cited by this paper
• Neuroanatomical substrates for paroxysmal dyskinesia in lethargic mice.

  2007cited by this paper
• Forward genetic screen of mouse reveals dominant missense mutation in the P/Q‐type voltage‐dependent calcium channel, CACNA1A

  2007cited by this paper
• CHAPTER C4 – Mouse Models of Dystonia

  2005cited by this paper
• Potassium Channel Blockers Inhibit the Triggers of Attacks in the Calcium Channel Mouse Mutant tottering

  2005cited by this paper
• Noradrenergic blockade prevents attacks in a model of episodic dysfunction caused by a channelopathy.

  2005cited by this paper
• CHAPTER A5 – Assessment of Movement Disorders in Rodents

  2005cited by this paper
• Two novel CACNA1A gene mutations associated with episodic ataxia type 2 and interictal dystonia.

  2005cited by this paper
• Abnormal motor behavior and vestibular dysfunction in the stargazer mouse mutant.

  2004cited by this paper
• Paroxysmal movement disorders in severe myoclonic epilepsy in infancy.

  2003cited by this paper
• Rating scales for dystonia: A multicenter assessment

  2003cited by this paper
• Insights from Mouse Models of Absence Epilepsy into Ca2+ Channel Physiology and Disease Etiology

  2002cited by this paper
• Benign paroxysmal torticollis of infancy: four new cases and linkage to CACNA1A mutation

  2002cited by this paper
• Triggers of paroxysmal dyskinesia in the calcium channel mouse mutant tottering.

  2002cited by this paper
• Paroxysmal Dyskinesias in the Lethargic Mouse Mutant

  2002cited by this paper
• Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.

  2001cited by this paper
• Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity

  2001cited by this paper
• Idiopathic Epilepsy and Paroxysmal Dyskinesia

  2001cited by this paper
• Rocker Is a New Variant of the Voltage-Dependent Calcium Channel Gene Cacna1a

  2001cited by this paper
• Episodic movement disorders as channelopathies.

  2000cited by this paper
• Episodic movement disorders as channelopathies

  2000cited by this paper
• Calcium channel agonists and dystonia in the mouse

  2000cited by this paper
• L-type calcium channels contribute to the tottering mouse dystonic episodes.

  1999cited by this paper
• Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit.

  1999cited by this paper
• Autosomal recessive Rolandic epilepsy with paroxysmal exercise‐induced dystonia and writer's cramp: Delineation of the syndrome and gene mapping to chromosome 16p12‐11.2

  1999cited by this paper
• CACNA1A mutations

  1999cited by this paper
• Clinical rating of dyskinesias in Parkinson's disease: Use and reliability of a new rating scale

  1999cited by this paper
• The paroxysmal dyskinesias

  1999cited by this paper
• Paroxysmal kinesigenic choreoathetosis: a report of 26 patients

  1999cited by this paper
• Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice

  1997cited by this paper
• Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p.

  1997cited by this paper
• Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16.

  1997cited by this paper
• Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.

  1996cited by this paper
• Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca Channel

  1996cited by this paper
• Absence epilepsy in tottering mutant mice is associated with calcium channel defects.

  1996cited by this paper
• Paroxysmal dyskinesias: Clinical features and classification

  1995cited by this paper
• Spontaneous polyspike discharges in an epileptic mutant mouse (tottering).

  1979cited by this paper

• Intra-putaminal muscarinic receptor agonist infusion induces a dystonic phenotype in non-human primate.

  2025cites this paper
• Cerebellar contributions to dystonia: unraveling the role of Purkinje cells and cerebellar nuclei

  2025cites this paper
• Cerebellar α1D- adrenergic receptors mediate stress-induced dystonia in totteringtg/tg mice

  2025cites this paper
• Sex Differences in Dystonia

  2024cites this paper
• Cerebellar α1D-adrenergic receptors mediate stress-induced dystonia in totteringtg/tg mice

  2023cites this paper
• BK channel properties correlate with neurobehavioral severity in three KCNMA1-linked channelopathy mouse models

  2022cites this paper
• Mechanism of stress-induced attacks in an episodic neurologic disorder

  2022cites this paper
• Discovery of the First Selective M4 Muscarinic Acetylcholine Receptor Antagonists with in Vivo Antiparkinsonian and Antidystonic Efficacy.

  2021cites this paper
• Cerebellar 5HT-2A receptor mediates stress-induced onset of dystonia

  2021cites this paper
• Relationship between physical exercise and the most varied forms of dyskinesia

  2021cites this paper
• Discovery of the first selective M4 muscarinic acetylcholine receptor antagonists with in vivo anti-parkinsonian and anti-dystonic efficacy

  2020cites this paper
• Tottering Mouse

  2019cites this paper
• Dystonia genes and their biological pathways.

  2019cites this paper
• Rôle du système cholinergique striatal dans la physiopathologie des dystonies : un modèle expérimental chez le primate non-humain

  2018cites this paper
• Aberrant cerebellar Purkinje cell activity as the cause of motor attacks in a mouse model of episodic ataxia type 2

  2018cites this paper
• Transcallosal conduction in paroxysmal kinesigenic dyskinesia

  2017cites this paper
• Parkinsonism without dopamine neuron degeneration in aged l‐dopa‐responsive dystonia knockin mice

  2017cites this paper
• Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.

  2017cites this paper
• Characterization of the dominant inheritance mechanism of Episodic Ataxia type 2.

  2017cites this paper
• Sleep fragmentation and Parkinson's disease pathology in older adults without Parkinson's disease

  2017cites this paper
• PRRT2 deficiency induces paroxysmal kinesigenic dyskinesia by regulating synaptic transmission in cerebellum

  2017cites this paper
• The Anatomical Basis for Dystonia: The Motor Network Model

  2017cites this paper
• A CaV2.1 N-terminal fragment relieves the dominant-negative inhibition by an Episodic ataxia 2 mutant

  2016cites this paper
• A new knockin mouse model of L-DOPA-responsive dystonia

  2015cites this paper
• Dystonia and cerebellar degeneration in the leaner mouse mutant.

  2015cites this paper
• A new knock-in mouse model of l-DOPA-responsive dystonia.

  2015cites this paper
• Mouse Models of Episodic Ataxia Type 2

  2015cites this paper
• Assessment of Movement Disorders in Rodents

  2015cites this paper
• Protein mutated in paroxysmal dyskinesia interacts with the active zone protein RIM and suppresses synaptic vesicle exocytosis

  2015cites this paper
• Flocculus Purkinje cell signals in mouse Cacna1a calcium channel mutants of escalating severity: an investigation of the role of firing irregularity in ataxia.

  2014cites this paper
• Genetic animal models of dystonia: common features and diversities.

  2014influential citation
• Subtle microstructural changes of the cerebellum in a knock-in mouse model of DYT1 dystonia.

  2014cites this paper
• The first knockin mouse model of episodic ataxia type 2.

  2014cites this paper
• RNAi silencing of P/Q-type calcium channels in Purkinje neurons of adult mouse leads to episodic ataxia type 2.

  2014cites this paper
• Limited regional cerebellar dysfunction induces focal dystonia in mice.

  2013influential citation
• The focal dystonias: Current views and challenges for future research

  2013cites this paper
• Stress, caffeine and ethanol trigger transient neurological dysfunction through shared mechanisms in a mouse calcium channelopathy.

  2013cites this paper
• Convergent mechanisms in etiologically-diverse dystonias

  2011cites this paper
• Selective Inhibition of Striatal Fast-Spiking Interneurons Causes Dyskinesias

  2011cites this paper
• The functional neuroanatomy of dystonia.

  2011cites this paper
• Purkinje Cell-Specific Ablation of CaV2.1 Channels is Sufficient to Cause Cerebellar Ataxia in Mice

  2011cites this paper
• Neuronal voltage-gated calcium channels

  2010cites this paper
• Kinematic and electromyographic tools for characterizing movement disorders in mice

  2010cites this paper
• Evidence-based guideline: The role of diffusion and perfusion MRI for the diagnosis of acute ischemic stroke

  2010cites this paper
• Therapeutics and Technology Assessment Subcommittee of the MRI for the diagnosis of acute ischemic stroke : Report of the Evidence-based guideline : The role of diffusion and perfusion

  2010cites this paper
• The Therapeutic Mode of Action of 4-Aminopyridine in Cerebellar Ataxia

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• NEURONAL VOLTAGE-GATED CALCIUM CHANNELS: BRIEF OVERVIEW OF THEIR FUNCTION AND CLINICAL IMPLICATIONS IN NEUROLOGY

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• Evidence-based guideline: The role of diffusion and perfusion MRI for the diagnosis of acute ischemic stroke

  2010cites this paper
• The basal ganglia and cerebellum interact in the expression of dystonic movement.

  2008cites this paper
• Purkinje Cell Input to Cerebellar Nuclei in Tottering: Ultrastructure and Physiology

  2008cites this paper
• Experimental therapeutics for dystonia

  2008cites this paper