Genetics of ion homeostasis in Ménière's Disease.

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RNA-sequencing study of peripheral blood mononuclear cells in sporadic Ménière's disease patients: possible contribution of immunologic dysfunction to the development of this disorder.Genes important for otoneurological diagnostic purposes - current status and future prospects

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Genetics of ion homeostasis in Ménière's Disease.

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http://www.wikidata.org/entity/Q39193364

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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name

Genetics of ion homeostasis in Ménière's Disease.

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Genetics of ion homeostasis in Ménière's Disease.

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type

Item

label

Genetics of ion homeostasis in Ménière's Disease.

@en

Genetics of ion homeostasis in Ménière's Disease.

@nl

prefLabel

Genetics of ion homeostasis in Ménière's Disease.

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Genetics of ion homeostasis in Ménière's Disease.

@nl

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Genetics of ion homeostasis in Ménière's Disease

@en

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Claudia Cassandro

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Mario Bussi

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Paolo Manunta

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Roberto Albera

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Simona Delli Carpini

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P2860

Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population

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

The International Classification of Headache Disorders, 3rd edition (beta version)

Identification of new signaling components in the sensory epithelium of human saccule.

Knockout of Na+/Ca2+ exchanger in smooth muscle attenuates vasoconstriction and L-type Ca2+ channel current and lowers blood pressure

Genes involved in vasoconstriction and vasodilation system affect salt-sensitive hypertension.

Accompanying Symptoms Overlap during Attacks in Menière's Disease and Vestibular Migraine

A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine

Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase.

Pathophysiology of Meniere's syndrome: are symptoms caused by endolymphatic hydrops?

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scholarly article

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10.1007/S00405-016-4375-9

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Genetics of ion homeostasis in Ménière's Disease.

about

P2860

P2860

Genetics of ion homeostasis in Ménière's Disease.

description

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P1433

P1476

P2093

P2860

P2888

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P698

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P1476

P2093

P2860

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P433

P478

P50

P577

P698