A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs (Q28285675)

11

object named as

Karin Jurkat-Rott

0 references

Liana Veneziano

object named as

Liana Veneziano

4

0 references

author name string

Maria Spadaro

1

0 references

Simona Ursu

2

0 references

Frank Lehmann-Horn

3

0 references

Veneziano Liana

5

0 references

Giovanni Antonini

6

0 references

Antonini Giovanni

7

0 references

Giunti Paola

9

0 references

Marina Frontali

Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A gene

10

0 references

language of work or name

English

0 references

publication date

September 2004

0 references

published in

Neurogenetics

0 references

volume

5

0 references

issue

3

0 references

page(s)

177-85

0 references

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-004-0183-2

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-004-0183-2

CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-004-0183-2

Cerebral hemodynamics in familial hemiplegic migraine

21 January 2018

1 reference

12 December 2020

Familial hemiplegic migraine

1 reference

12 December 2020

A gene for familial hemiplegic migraine maps to chromosome 19

1 reference

12 December 2020

Episodes of acute confusion or psychosis in familial hemiplegic migraine

1 reference

12 December 2020

Familial migraine coma: a case study

1 reference

12 December 2020

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

1 reference

12 December 2020

Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group

1 reference

12 December 2020

Importance of transmembrane segment M3 of the sarcoplasmic reticulum Ca2+-ATPase for control of the gateway to the Ca2+ sites

1 reference

12 December 2020

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

1 reference

12 December 2020

Strategies for multilocus linkage analysis in humans

1 reference

12 December 2020

Familial hemiplegic migraine with crossed cerebellar diaschisis and unilateral meningeal enhancement

1 reference

12 December 2020

Multimodal functional imaging of prolonged neurological deficits in a patient suffering from familial hemiplegic migraine

1 reference

12 December 2020

Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23

1 reference

12 December 2020

The International Classification of Headache Disorders: 2nd edition

1 reference

12 December 2020

Recurrent Episodes of Coma: An Unusual Phenotype of Familial Hemiplegic Migraine with Linkage to Chromosome 1

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

Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family

1 reference

12 December 2020

A new locus for hemiplegic migraine maps to chromosome 1q31

1 reference

12 December 2020

Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia

1 reference

12 December 2020

Migraine coma. Meningitic migraine with cerebral oedema associated with a new form of autosomal dominant cerebellar ataxia

1 reference

12 December 2020

Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions

1 reference

12 December 2020

A typical migraine susceptibility region localizes to chromosome 1q31

1 reference

12 December 2020

Familial hemiplegic migraine with irreversible brain damage.

1 reference

12 December 2020

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

1 reference

12 December 2020

Hemiplegic migraine induced by exertion

1 reference

12 December 2020

Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family

1 reference

12 December 2020

Familial hemiplegic migraine versus migraine with prolonged aura: an uncertain diagnosis in a family report.

1 reference

12 December 2020

Familial hemiplegic migraine in The Netherlands. Dutch Migraine Genetics Research Group

1 reference

12 December 2020

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

1 reference

12 December 2020

Serial MRI in a case of familial hemiplegic migraine

1 reference

12 December 2020

Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine

1 reference

12 December 2020

Prolonged hemiplegic migraine associated with unilateral hyperperfusion on perfusion weighted magnetic resonance imaging

1 reference

12 December 2020

Variation is now the theme

1 reference

12 December 2020

Footballer's migraine--a report of 2 cases

1 reference

12 December 2020