(Q33921453)

30 July 2017

title

Paroxysmal dyskinesias in mice (English)

1 reference

30 July 2017

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Thomas L Shirley

1

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30 July 2017

Lekha M Rao

series ordinal

2

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30 July 2017

Ellen J Hess

series ordinal

3

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30 July 2017

H A Jinnah

series ordinal

4

1 reference

30 July 2017

language of work or name

English

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publication date

1 January 2008

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30 July 2017

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30 July 2017

volume

23

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30 July 2017

issue

2

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30 July 2017

page(s)

259-264

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The ataxic groggy rat has a missense mutation in the P/Q-type voltage-gated Ca2+ channel alpha1A subunit gene and exhibits absence seizures

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

Insights from mouse models of absence epilepsy into Ca2+ channel physiology and disease etiology

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

Paroxysmal dyskinesias in the lethargic mouse mutant

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

Idiopathic epilepsy and paroxysmal dyskinesia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

Rocker is a new variant of the voltage-dependent calcium channel gene Cacna1a

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

The paroxysmal dyskinesias

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

Paroxysmal kinesigenic choreoathetosis: a report of 26 patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

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.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

L-type calcium channels contribute to the tottering mouse dystonic episodes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

Familial Infantile Convulsions and Paroxysmal Choreoathetosis: A New Neurological Syndrome Linked to the Pericentromeric Region of Human Chromosome 16

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

Absence epilepsy in tottering mutant mice is associated with calcium channel defects

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

Paroxysmal dyskinesias: clinical features and classification

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

Triggers of paroxysmal dyskinesia in the calcium channel mouse mutant tottering

5 July 2018

1 reference

Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse

21 January 2018

1 reference

Rating scales for dystonia: a multicenter assessment.

21 January 2018

1 reference

Abnormal motor behavior and vestibular dysfunction in the stargazer mouse mutant.

21 January 2018

1 reference

Neuroanatomical substrates for paroxysmal dyskinesia in lethargic mice

21 January 2018

1 reference

Noradrenergic blockade prevents attacks in a model of episodic dysfunction caused by a channelopathy

21 January 2018

1 reference

Two novel CACNA1A gene mutations associated with episodic ataxia type 2 and interictal dystonia

21 January 2018

1 reference

Paroxysmal movement disorders in severe myoclonic epilepsy in infancy

21 January 2018

1 reference

Potassium channel blockers inhibit the triggers of attacks in the calcium channel mouse mutant tottering.

21 January 2018

1 reference

Forward genetic screen of mouse reveals dominant missense mutation in the P/Q-type voltage-dependent calcium channel, CACNA1A.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

Motor and cognitive deficits in the heterozygous leaner mouse, a Cav2.1 voltage-gated Ca2+ channel mutant

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887756

Episodic movement disorders as channelopathies

29 October 2018

1 reference

12 December 2020

Calcium channel agonists and dystonia in the mouse

1 reference

12 December 2020

Benign paroxysmal torticollis of infancy: four new cases and linkage to CACNA1A mutation

1 reference

12 December 2020

Spontaneous polyspike discharges in an epileptic mutant mouse (tottering)

1 reference

12 December 2020

Clinical rating of dyskinesias in Parkinson's disease: use and reliability of a new rating scale

1 reference

12 December 2020

CACNA1A mutations: hemiplegic migraine, episodic ataxia type 2, and the others

1 reference

12 December 2020

Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice

1 reference

12 December 2020

Identifiers

DOI

10.1002/MDS.21829

1 reference

release_3jpoupn52vf7fo6qb6holbec7e

30 July 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/3jpoupn52vf7fo6qb6holbec7e

24 November 2022

mapped directly with Wikidata item

PMC publication ID

2887756

1 reference

30 July 2017

1 reference