(Q37205369)

18 August 2017

0 references

A locus for migraine without aura maps on chromosome 14q21.2-q22.3. (English)

1 reference

18 August 2017

1 reference

migraine without aura

1 reference

A Vettori

2

0 references

Rossella Tupler

object named as

R Tupler

7

0 references

author name string

D Soragna

1

1 reference

18 August 2017

G Carraro

3

1 reference

18 August 2017

E Marchioni

4

1 reference

18 August 2017

G Vazza

5

1 reference

18 August 2017

S Bellini

6

1 reference

18 August 2017

F Savoldi

8

1 reference

18 August 2017

M L Mostacciuolo

9

1 reference

18 August 2017

language of work or name

English

0 references

publication date

9 December 2002

1 reference

American Journal of Human Genetics

18 August 2017

1 reference

18 August 2017

72

1 reference

18 August 2017

1

1 reference

18 August 2017

161-167

1 reference

A susceptibility locus for migraine with aura, on chromosome 4q24.

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Prostaglandins and leukotrienes: advances in eicosanoid biology

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Pathophysiology of migraine--new insights.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Altered allelic distributions of the serotonin transporter gene in migraine without aura and migraine with aura

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

A new locus for hemiplegic migraine maps to chromosome 1q31

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

The trigeminovascular system and migraine: studies characterizing cerebrovascular and neuropeptide changes seen in humans and cats.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

A gene for familial hemiplegic migraine maps to chromosome 19

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Pathophysiology of the migraine aura. The spreading depression theory

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Prevalence and sex-ratio of the subtypes of migraine.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Easy calculations of lod scores and genetic risks on small computers

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Prevalence of migraine headache in the United States. Relation to age, income, race, and other sociodemographic factors

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Vasoactive peptide release in the extracerebral circulation of humans during migraine headache

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Biosynthesis of nitric oxide: dependence on pteridine metabolism

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

The genetics of migraine without aura and migraine with aura

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Cloning, sequencing and functional studies of the gene encoding human GTP cyclohydrolase I.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Familial typical migraine: significant linkage and localization of a gene to Xq24-28.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Activin and bone morphogenetic proteins induce calcitonin gene-related peptide in embryonic sensory neurons in vitro

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Inheritance of migraine investigated by complex segregation analysis.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Association between migraine and endothelin type A receptor (ETA -231 A/G) gene polymorphism.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Evidence for allelic association of the dopamine beta-hydroxylase gene (DBH) with susceptibility to typical migraine

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Evidence of a genetic factor in migraine with aura: a population-based Danish twin study

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

A procedure for combining two-point lod scores into a summary multipoint map.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Migraine and concomitant symptoms among 8167 adult twin pairs.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Testing Models for Genetic Determination in Migraine

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378621

Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura

4 December 2018

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

Genetic markers: association study in migraine

1 reference

12 December 2020

Familial risk of migraine: A population-based study

1 reference

12 December 2020

Clinical susceptibility to migraine with aura is modified by dopamine D2 receptor (DRD2) NcoI alleles

1 reference

12 December 2020

Association between dopamine receptor genes and migraine without aura in a Sardinian sample

1 reference

12 December 2020

Migraine without aura: A population-based twin study

1 reference

12 December 2020

A typical migraine susceptibility region localizes to chromosome 1q31

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

Identifiers

DOI

10.1086/345298

1 reference

18 August 2017

1 reference

18 August 2017

1 reference