(Q51054045)

English

Finnish familial Meniere disease is not linked to chromosome 12p12.3, and anticipation and cosegregation with migraine are not common findings.

scientific article published in May 2011

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scholarly article

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Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/21346584

Finnish familial Meniere disease is not linked to chromosome 12p12.3, and anticipation and cosegregation with migraine are not common findings. (English)

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/21346584

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1 reference

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author name string

Elina Hietikko

1

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/21346584

Jouko Kotimäki

2

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/21346584

Erna Kentala

3

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/21346584

Tuomas Klockars

4

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/21346584

Martti Sorri

5

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/21346584

Minna Männikkö

6

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/21346584

language of work or name

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publication date

1 May 2011

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/21346584

Genetics in Medicine

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/21346584

13

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/21346584

5

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/21346584

415-420

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/21346584

https://scigraph.springernature.com/pub.10.1097/gim.0b013e3182091a41

0 references

The basic science of Meniere's disease and endolymphatic hydrops

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

Prevalence of Meniere disease in Finland.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

Familial Ménière's disease: clinical and genetic aspects.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

Inheritance of Meniere's disease in the Finnish population.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

The relevance of migraine in patients with Meńière's disease

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

Epidemiology of vertigo, migraine and vestibular migraine

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

Ménière's disease is associated with single nucleotide polymorphisms in the human potassium channel genes, KCNE1 and KCNE3

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

Polymorphic analysis of the heat-shock protein 70 gene (HSPA1A) in Ménière's disease.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

Gly460Trp alpha-adducin mutation as a possible mechanism leading to endolymphatic hydrops in Ménière's syndrome.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

Sequence variants in host cell factor C1 are associated with Ménière's disease

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

Poly(ADP-ribose) polymerase-1 (PARP-1) longer alleles spanning the promoter region may confer protection to bilateral Meniere's disease.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

A Meniere's disease gene linked to chromosome 12p12.3.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

Genetics (molecular biology) and Meniere's disease

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

Advanced Meniere's Disease:A Study of 356 Severely Disabled Patients

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

Familial clustering of migraine, episodic vertigo, and Ménière's disease

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

Familiar Meniere's disease restricted to 1.48 Mb on chromosome 12p12.3 by allelic and haplotype association.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

Ménière's Disease in Males and Females

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182091A41

21 January 2018

Identifiers

10.1097/GIM.0B013E3182091A41

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/21346584

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/21346584

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