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Article

P/Q-type Ca2+ channel defects in migraine, ataxia and epilepsy.

Trends in pharmacological sciences - 1 Apr 1998

Ophoff R A, Terwindt G M, Frants R R, Ferrari M D

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 9612085
DOI: 10.1016/s0165-6147(98)01182-1

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P/Q-type Ca2+ channel defects in migraine, ataxia and epilepsy.PMID 9612085Read ↗

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The role of calcium channel mutations in human epilepsy.Semantic proximity Read ↗

Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS.Semantic proximity Read ↗

Clusters of non-truncating mutations of P/Q type Ca2+ channel subunit Ca(v)2.1 causing episodic ataxia 2.Semantic proximity Read ↗

CaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder Including Arrhythmia and AutismSemantic proximity Read ↗

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Genetic Calcium Signaling Abnormalities in the Central Nervous System: Seizures, Migraine, and AutismSemantic proximity Read ↗

CACNA1A-Related Channelopathies: Clinical Manifestations and Treatment Options.Semantic proximity Read ↗

Mutant P/Q-type calcium channel electrophysiology and migraine.Semantic proximity Read ↗

[Calcium channel mutations and disorders of synaptic transmission].Semantic proximity Read ↗

Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channelsSemantic proximity Read ↗

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