(Q28295213)

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G M Terwindt

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M N Vergouwe

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R van Eijk

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P J Oefner

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S M Hoffman

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J E Lamerdin

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H W Mohrenweiser

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D E Bulman

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J Haan

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G J van Ommen

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M H Hofker

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M D Ferrari

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R R Frants

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1

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language of work or name

English

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publication date

1 November 1996

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543-52

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Ion-channel defects and aberrant excitability in myotonia and periodic paralysis

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Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

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Chromosomal localization of the human genes for alpha 1A, alpha 1B, and alpha 1E voltage-dependent Ca2+ channel subunits

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On serotonin and migraine: a clinical and pharmacological review

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5-HT1 receptors in migraine pathophysiology and treatment

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Serotonin metabolism in migraine

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Episodic ataxias as channelopathies

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Developing three-dimensional models of ion channel proteins

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

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The skeletal muscle sodium and chloride channel diseases

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A gene for familial hemiplegic migraine maps to chromosome 19

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A calcium channel mutation causing hypokalemic periodic paralysis

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Characterization of cDNA clones containing CCA trinucleotide repeats derived from human brain

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Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura

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Primary structure and functional expression from complementary DNA of a brain calcium channel

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Neurogenic versus vascular mechanisms of sumatriptan and ergot alkaloids in migraine

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Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

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Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

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Identification of a mutation in the gene causing hyperkalemic periodic paralysis

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Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

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Low brain magnesium in migraine

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Primary structure of a calcium channel that is highly expressed in the rat cerebellum

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Primary structure of the receptor for calcium channel blockers from skeletal muscle

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Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p

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Magnesium regulates intracellular free ionized calcium concentration and cell geometry in vascular smooth muscle cells

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Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

8898206

1 reference

Consolidated OpenCitations Corpus – April 2017