(Q28295213)

10

object named as

M Ferrari

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author name string

R A Ophoff

1

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G M Terwindt

2

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M N Vergouwe

3

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R van Eijk

4

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P J Oefner

5

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S M Hoffman

6

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J E Lamerdin

7

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H W Mohrenweiser

8

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D E Bulman

9

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J Haan

11

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G J van Ommen

13

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M H Hofker

14

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M D Ferrari

15

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R R Frants

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

16

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language of work or name

English

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publication date

1 November 1996

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published in

Cell

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volume

87

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page(s)

543-52

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issue

3

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cites work

1 reference

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7 January 2021

Exon amplification: a strategy to isolate mammalian genes based on RNA splicing

1 reference

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7 January 2021

The biochemistry and molecular biology of the dihydropyridine-sensitive calcium channel

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7 January 2021

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

1 reference

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7 January 2021

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

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7 January 2021

Structural and functional diversity of voltage-activated calcium channels.

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981373-2

7 January 2021

Familial hemiplegic migraine, nystagmus, and cerebellar atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981373-2

7 January 2021

On serotonin and migraine: a clinical and pharmacological review

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7 January 2021

5-HT1 receptors in migraine pathophysiology and treatment

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7 January 2021

Serotonin metabolism in migraine

1 reference

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7 January 2021

Episodic ataxias as channelopathies

1 reference

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7 January 2021

Developing three-dimensional models of ion channel proteins

1 reference

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7 January 2021

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

1 reference

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7 January 2021

The skeletal muscle sodium and chloride channel diseases

1 reference

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7 January 2021

A gene for familial hemiplegic migraine maps to chromosome 19

1 reference

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7 January 2021

A calcium channel mutation causing hypokalemic periodic paralysis

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Neurogenic versus vascular mechanisms of sumatriptan and ergot alkaloids in migraine

1 reference

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7 January 2021

Genetic heterogeneity of familial hemiplegic migraine

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Prophylaxis of migraine with oral magnesium: results from a prospective, multi-center, placebo-controlled and double-blind randomized study

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981373-2

7 January 2021

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981373-2

7 January 2021

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981373-2

7 January 2021

Low brain magnesium in migraine

1 reference

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7 January 2021

Sensitivity of single-strand conformation polymorphism and heteroduplex method for mutation detection in the cystic fibrosis gene.

1 reference

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7 January 2021

Increased familial risk and evidence of genetic factor in migraine

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981373-2

7 January 2021

Prevalence and sex-ratio of the subtypes of migraine.

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981373-2

7 January 2021

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

1 reference

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7 January 2021

Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RG

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981373-2

7 January 2021

10.1016/S0092-8674(00)81373-2

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

640232

640232

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference