Familial clustering and genetic heterogeneity in Meniere's disease.
about
Acupuncture Points Stimulation for Meniere's Disease/Syndrome: A Promising Therapeutic Approach.Genetics of vestibular disorders: pathophysiological insightsGenetics of Tinnitus: An Emerging Area for Molecular Diagnosis and Drug DevelopmentAutoimmunity as a candidate for the etiopathogenesis of Meniere's disease: detection of autoimmune reactions and diagnostic biomarker candidateA pipeline combining multiple strategies for prioritizing heterozygous variants for the identification of candidate genes in exome datasetsIdentification of two novel mutations in FAM136A and DTNA genes in autosomal-dominant familial Meniere's disease.The genetics of Ménière's disease.Familial clustering of overweight and obesity among schoolchildren in northern ChinaAltered chromogranin A circulating levels in Meniere's disease.Clinical Subgroups in Bilateral Meniere Disease.Population-Based Study on the Epidemiology of Ménière's Disease.Variants in the KCNE1 or KCNE3 gene and risk of Ménière's disease: A meta-analysis.Caffeine intake and Menière's disease: Is there relationship?A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease.Genetic aspects and clinical characteristics of familial Meniere's disease in a South Korean population.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.Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease.Extended phenotype and clinical subgroups in unilateral Meniere disease: A cross-sectional study with cluster analysis.Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere's Disease.[Diagnostic criteria for Menière's disease according to the Classification Committee of the Bárány Society].Genetics of presbycusis and presbystasis.Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease.X-Linked Sensorineural Hearing Loss: A Literature ReviewTowards personalized medicine in Ménière’s disease
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P2860
Familial clustering and genetic heterogeneity in Meniere's disease.
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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2013年学术文章
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2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
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2013年學術文章
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name
Familial clustering and genetic heterogeneity in Meniere's disease.
@en
Familial clustering and genetic heterogeneity in Meniere's disease.
@nl
type
label
Familial clustering and genetic heterogeneity in Meniere's disease.
@en
Familial clustering and genetic heterogeneity in Meniere's disease.
@nl
prefLabel
Familial clustering and genetic heterogeneity in Meniere's disease.
@en
Familial clustering and genetic heterogeneity in Meniere's disease.
@nl
P2093
P2860
P50
P356
P1433
P1476
Familial clustering and genetic heterogeneity in Meniere's disease
@en
P2093
A Soto-Varela
S Santos-Perez
P2860
P304
P356
10.1111/CGE.12150
P50
P577
2013-04-09T00:00:00Z