(Q57956175)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

title

CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference

alternating hemiplegia of childhood

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Johannes-peter Haas

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

author name string

B de Vries

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

H Lauffer

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

J Haan

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

A H Stam

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

A M J M van den Maagdenberg

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

K R J Vanmolkot

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Laem Laan

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

I B Ginjaar

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

R R Frants

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

G M Terwindt

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

M D Ferrari

13

1 reference

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7 January 2020

language of work or name

English

0 references

publication date

21 May 2008

1 reference

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7 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

volume

28

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

issue

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

page(s)

887-891

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene.

7 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01596.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01596.X

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01596.X

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01596.X

Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01596.X

A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01596.X

A simple salting out procedure for extracting DNA from human nucleated cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01596.X

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01596.X

Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01596.X

Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01596.X

Alternating hemiplegia of childhood: no mutations in the glutamate transporter EAAT1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01596.X

New insights into migraine pathophysiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01596.X

Migraine: gene mutations and functional consequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-2982.2008.01596.X

10.1111/J.1468-2982.2008.01596.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18498393%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference