(Q60205163)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9412851%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

title

Searching for migraine genes: exclusion of 290 cM out of the whole human genome (English)

1 reference

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8 November 2019

1 reference

9

1 reference

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8 November 2019

author name string

L Monari

1

1 reference

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8 November 2019

M Mochi

2

1 reference

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8 November 2019

M L Valentino

3

1 reference

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8 November 2019

C Arnaldi

4

1 reference

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8 November 2019

P Cortelli

5

1 reference

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8 November 2019

A De Monte

6

1 reference

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8 November 2019

G Pierangeli

7

1 reference

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8 November 2019

G Prologo

8

1 reference

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8 November 2019

S Soriani

10

1 reference

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8 November 2019

P Montagna

11

1 reference

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8 November 2019

publication date

1 October 1997

1 reference

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8 November 2019

number of pages

6

1 reference

Italian journal of neurological sciences

inferred from page(s)

published in

1 reference

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8 November 2019

volume

18

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8 November 2019

page(s)

277-282

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8 November 2019

issue

5

1 reference

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A gene for familial hemiplegic migraine maps to chromosome 19

8 November 2019

cites work

1 reference

12 December 2020

Testing Models for Genetic Determination in Migraine

1 reference

12 December 2020

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

1 reference

12 December 2020

The 1993-94 Généthon human genetic linkage map

1 reference

12 December 2020

Genetic mapping of the beta 1- and gamma-subunits of the human skeletal muscle L-type voltage-dependent calcium channel on chromosome 17q and exclusion as candidate genes for malignant hyperthermia susceptibility

1 reference

12 December 2020

Genetic heterogeneity of familial hemiplegic migraine

1 reference

12 December 2020

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

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

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

1 reference

12 December 2020

Skeletal muscle and brain isoforms of a beta-subunit of human voltage-dependent calcium channels are encoded by a single gene

1 reference

12 December 2020

Familial Migraine: Exclusion of the Susceptibility Gene from the Reported Locus of Familial Hemiplegic Migraine on 19p

1 reference

12 December 2020

Exclusion of 5-HT2A and 5-HT2C receptor genes as candidate genes for migraine

1 reference

12 December 2020

Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain. Headache Classification Committee of the International Headache Society

1 reference

12 December 2020

Migraine association and linkage analyses of the human 5-hydroxytryptamine (5HT2A) receptor gene.

1 reference

12 December 2020

A null allele for the Afm175xg3 marker at locus D17S795 caused by a primer binding failure

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02083304

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9412851%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

1 reference