(Q28268080)

3

object named as

Karin Jurkat-Rott

0 references

Christian Kubisch

13

object named as

Christian Kubisch

0 references

Hartmut Göbel

12

object named as

Hartmut Göbel

0 references

author name string

Unda Todt

1

0 references

Axel Heinze

4

0 references

Giovanni Zifarelli

5

0 references

Jan B Koenderink

6

0 references

Ingrid Goebel

7

0 references

Vera Zumbroich

8

0 references

Anne Stiller

9

0 references

Alfredo Ramirez

10

0 references

Thomas Friedrich

Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants

11

0 references

language of work or name

English

0 references

publication date

October 2005

0 references

published in

Human Mutation

0 references

volume

26

0 references

issue

4

0 references

page(s)

315-21

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cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

Symptomatic and nonsymptomatic headaches in a general population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

Increased familial risk and evidence of genetic factor in migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

Evolution of substrate specificities in the P-type ATPase superfamily.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Localization of a gene for migraine without aura to chromosome 4q21.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Significant linkage to migraine with aura on chromosome 11q24.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Update on the genetics of migraine

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Multiple rare variants in different genes account for multifactorial inherited susceptibility to colorectal adenomas

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Migraine--current understanding and treatment

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Functional differences between alpha subunit isoforms of the rat Na,K-ATPase expressed in Xenopus oocytes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

No mutations in CACNA1A and ATP1A2 in probands with common types of migraine

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Biochemistry of Na,K-ATPase

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Electrophysiological Analysis of the Mutated Na,K-ATPase Cation Binding Pocket

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Prevalence and burden of migraine in the United States: data from the American Migraine Study II.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

The global burden of disease study: implications for neurology

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Flunarizine in prophylaxis of childhood migraine. A double-blind, placebo-controlled, crossover study.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

The International Classification of Headache Disorders: 2nd edition

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Structure-function relationships in the Na,K-ATPase alpha subunit: site-directed mutagenesis of glutamine-111 to arginine and asparagine-122 to aspartic acid generates a ouabain-resistant enzyme

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Are rare variants responsible for susceptibility to complex diseases?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

https://api.crossref.org/works/10.1002%2FHUMU.20229

1 reference

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

Crystal structure of the calcium pump of sarcoplasmic reticulum at 2.6 A resolution

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20229

7 January 2021