(Q46448193)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15843617%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

title

Potassium channel blockers inhibit the triggers of attacks in the calcium channel mouse mutant tottering (English)

1 reference

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11 January 2020

1 reference

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11 January 2020

Robert S Raike

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15843617%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

Luis E Soria-Jasso

series ordinal

1 reference

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11 January 2020

Ellen J Hess

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15843617%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

language of work or name

English

0 references

publication date

1 April 2005

1 reference

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11 January 2020

published in

Journal of Neuroscience

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11 January 2020

volume

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11 January 2020

issue

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11 January 2020

page(s)

4141-4145

1 reference

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High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2

11 January 2020

cites work

1 reference

12 December 2020

Calcium channelopathies in the central nervous system

1 reference

12 December 2020

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia

1 reference

12 December 2020

Molecular diversity of K+ channels

1 reference

12 December 2020

Episodic movement disorders as channelopathies

1 reference

12 December 2020

Calcium channel agonists and dystonia in the mouse

1 reference

12 December 2020

Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2

1 reference

12 December 2020

Highly 4-aminopyridine sensitive delayed rectifier current modulates the excitability of guinea pig cerebellar Purkinje cells.

1 reference

12 December 2020

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

1 reference

12 December 2020

Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission

1 reference

12 December 2020

Functional consequences of P/Q-type Ca2+ channel Cav2.1 missense mutations associated with episodic ataxia type 2 and progressive ataxia

1 reference

12 December 2020

Triggers of paroxysmal dyskinesia in the calcium channel mouse mutant tottering

1 reference

12 December 2020

Treatment of downbeat nystagmus with 3,4-diaminopyridine: a placebo-controlled study

1 reference

12 December 2020

Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita

1 reference

12 December 2020

Novel CACNA1A mutation causes febrile episodic ataxia with interictal cerebellar deficits

1 reference

12 December 2020

Dendritic control of spontaneous bursting in cerebellar Purkinje cells.

1 reference

12 December 2020

Treatment of episodic ataxia type 2 with the potassium channel blocker 4-aminopyridine

1 reference

12 December 2020

Functional implications of a novel EA2 mutation in the P/Q-type calcium channel.

1 reference

12 December 2020

Presynaptic Ca2+ channels compete for channel type-preferring slots in altered neurotransmission arising from Ca2+ channelopathy

1 reference

12 December 2020

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

1 reference

12 December 2020

On the active form of 4-aminopyridine: block of K+ currents in rabbit Schwann cells

1 reference

12 December 2020

Effects of several aminopyridines and analogs on the calcium dependence of synaptic transmission

1 reference

12 December 2020

Localization and functional properties of a rat brain alpha 1A calcium channel reflect similarities to neuronal Q- and P-type channels

1 reference

12 December 2020

Episodic ataxias as channelopathies

1 reference

12 December 2020

Localization of mRNAs of voltage-dependent Ca2+-channels: four subtypes of α1- and β-subunits in developing and mature rat brain

1 reference

12 December 2020

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

1 reference

12 December 2020

The expression of neuronal voltage-dependent calcium channels in human cerebellum

1 reference

12 December 2020

A method for determining 4-aminopyridine in plasma: pharmacokinetics in anaesthetized guinea pigs after intravenous administration

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Channelopathies: ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous system

1 reference

12 December 2020

Episodic ataxia and channelopathies

1 reference

12 December 2020

Cerebellar circuitry is activated during convulsive episodes in the tottering (tg/tg) mutant mouse

1 reference

12 December 2020

Single tottering mutations responsible for the neuropathic phenotype of the P-type calcium channel

1 reference

12 December 2020

10.1523/JNEUROSCI.0098-05.2005

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15843617%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15843617%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

PubMed publication ID

15843617

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15843617%20AND%20SRC:MED&resulttype=core&format=json