Phenotypic and genetic analysis of a large family with migraine-associated vertigo. - Wikidata - awgldk - TriplyDB

Phenotypic and genetic analysis of a large family with migraine-associated vertigo.

Phenotypic and genetic analysis of a large family with migraine-associated vertigo.

http://www.wikidata.org/entity/Q33756975

about

ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome Headaches of otolaryngological interest: current status while awaiting revision of classification. Practical considerations and expectations.New insights into pathophysiology of vestibular migraine The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition Association of benign recurrent vertigo and migraine in 208 patients.Migraine-associated vertigo: diagnosis and treatment.Headache and Dizziness: How to Differentiate Vestibular Migraine from Other Conditions.Meniere's Disease and Vestibular Migraine: Updates and Review of the Literature Genetics of presbycusis and presbystasis.

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Phenotypic and genetic analysis of a large family with migraine-associated vertigo.

http://www.wikidata.org/entity/Q33756975

description

2007 nî lūn-bûn

@nan

2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2007年の論文

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2007年論文

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2007年論文

@zh-hant

2007年論文

@zh-hk

2007年論文

@zh-mo

2007年論文

@zh-tw

2007年论文

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name

Phenotypic and genetic analysis of a large family with migraine-associated vertigo.

@ast

Phenotypic and genetic analysis of a large family with migraine-associated vertigo.

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type

label

Phenotypic and genetic analysis of a large family with migraine-associated vertigo.

@ast

Phenotypic and genetic analysis of a large family with migraine-associated vertigo.

@en

prefLabel

Phenotypic and genetic analysis of a large family with migraine-associated vertigo.

@ast

Phenotypic and genetic analysis of a large family with migraine-associated vertigo.

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Phenotypic and genetic analysis of a large family with migraine-associated vertigo.

@en

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Hane Lee

http://www.w3.org/2001/XMLSchema#string

Joanna C Jen

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Robert W Baloh

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Stanley F Nelson

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Yoon-Hee Cha

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P2860

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

Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine

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

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

Genomewide significant linkage to migrainous headache on chromosome 5q21.

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

Genes and migraine.

Epidemiology of vertigo.

Benign recurrent vertigo.

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1460-1467

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10.1111/J.1526-4610.2007.01002.X

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18081823

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migraine disorder

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