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Identification of two novel mutations in FAM136A and DTNA genes in autosomal-dominant familial Meniere's disease

Human molecular genetics, 2015-02, Vol.24 (4), p.1119-1126

2015

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Innovations in Doctoral Training and Research on Tinnitus: The European School on Interdisciplinary Tinnitus Research (ESIT) Perspective

Frontiers in aging neuroscience, 2018-01, Vol.9, p.447-447

2018

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A Systematic Review on the Association of Acquired Human Cytomegalovirus Infection with Hearing Loss

Journal of clinical medicine, 2020-12, Vol.9 (12), p.4011

2020

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The pharmacological management of vertigo in Meniere disease

Expert opinion on pharmacotherapy, 2020-09, Vol.21 (14), p.1753-1763

2020

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A Systematic Review on Heritability of Sudden Sensorineural Hearing Loss

The Laryngoscope, 2024-08, Vol.134 (8), p.3447-3457

2024

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Polymorphisms of CD16A and CD32 Fcγ receptors and circulating immune complexes in Ménière's disease: a case-control study

BMC medical genetics, 2011-01, Vol.12 (1), p.2-2, Article 2

2011

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Immune-Related Disorders Associated With Ménière's Disease: A Systematic Review and Meta-analysis

Otolaryngology-head and neck surgery, 2023-11, Vol.169 (5), p.1122-1131

2023

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Diagnostic criteria for Menière's disease. Consensus document of the Bárány Society, the Japan Society for Equilibrium Research, the European Academy of Otology and Neurotology (EAONO), the American Academy of Otolaryngology-Head and Neck Surgery (AAO-HNS) and the Korean Balance Society

Acta otorrinolaringologica espanola, 2016-01, Vol.67 (1), p.1

2016

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Diagnostic criteria for Menière's disease

Journal of vestibular research, 2015-01, Vol.25 (1), p.1-7

2015

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Genetics of vestibular disorders: pathophysiological insights

Journal of Neurology, 2016-04, Vol.263 (Suppl 1), p.45-53

2016

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A tinnitus symphony in 100 patients with Meniere's disease

Clinical otolaryngology, 2019-11, Vol.44 (6), p.1176-1180

2019

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Systematic review of magnetic resonance imaging for diagnosis of Meniere disease

Journal of vestibular research, 2019-01, Vol.29 (2-3), p.121-129

2019

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Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus

Npj genomic medicine, 2022-11, Vol.7 (1), p.70-9, Article 70

2022

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Types of Inheritance and Genes Associated with Familial Meniere Disease

Journal of the Association for Research in Otolaryngology, 2023-06, Vol.24 (3), p.269-279

2023

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Defective α‐tectorin may involve tectorial membrane in familial Meniere disease

Clinical and translational medicine, 2022-06, Vol.12 (6), p.e829-n/a

2022

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Systematic Review of Prevalence Studies and Familial Aggregation in Vestibular Migraine

Frontiers in genetics, 2020-08, Vol.11, p.954-954

2020

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Genetics of Recurrent Vertigo and Vestibular Disorders

Current genomics, 2011-09, Vol.12 (6), p.443-450

2011

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Multiomic-based immune response profiling in migraine, vestibular migraine and Meniere's disease

Immunology, 2024-09

2024

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Correction: A systematic review on the contribution of DNA methylation to hearing loss

Clinical epigenetics, 2024-09, Vol.16 (1), p.129-2, Article 129

2024

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A systematic review on the contribution of DNA methylation to hearing loss

Clinical epigenetics, 2024-07, Vol.16 (1), p.88-15, Article 88

2024

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High prevalence of systemic autoimmune diseases in patients with Menière's disease

PloS one, 2011, Vol.6 (10), p.e26759-e26759

2011

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Association of a functional polymorphism of PTPN22 encoding a lymphoid protein phosphatase in bilateral Meniere's disease

The Laryngoscope, 2010-01, Vol.120 (1), p.103-107

2010

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Epidemiology and genetics of Meniere's disease

Current opinion in neurology, 2024-02, Vol.37 (1), p.88-94

2024

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Excess of Rare Missense Variants in Hearing Loss Genes in Sporadic Meniere Disease

Frontiers in genetics, 2019-02, Vol.10, p.76

2019

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Identification of two novel mutations in FAM136A and DTNA genes in autosomal-dominant familial Meniere's disease

Innovations in Doctoral Training and Research on Tinnitus: The European School on Interdisciplinary Tinnitus Research (ESIT) Perspective

A Systematic Review on the Association of Acquired Human Cytomegalovirus Infection with Hearing Loss

The pharmacological management of vertigo in Meniere disease

Clinical Features, Familial History, and Migraine Precursors in Patients With Definite Vestibular Migraine: The VM‐Phenotypes Projects

A Systematic Review on Heritability of Sudden Sensorineural Hearing Loss

Polymorphisms of CD16A and CD32 Fcγ receptors and circulating immune complexes in Ménière's disease: a case-control study

Immune-Related Disorders Associated With Ménière's Disease: A Systematic Review and Meta-analysis

Diagnostic criteria for Menière's disease. Consensus document of the Bárány Society, the Japan Society for Equilibrium Research, the European Academy of Otology and Neurotology (EAONO), the American Academy of Otolaryngology-Head and Neck Surgery (AAO-HNS) and the Korean Balance Society

Diagnostic criteria for Menière's disease

Genetics of vestibular disorders: pathophysiological insights

A tinnitus symphony in 100 patients with Meniere's disease

Systematic review of magnetic resonance imaging for diagnosis of Meniere disease

Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus

Types of Inheritance and Genes Associated with Familial Meniere Disease

Defective α‐tectorin may involve tectorial membrane in familial Meniere disease

Systematic Review of Prevalence Studies and Familial Aggregation in Vestibular Migraine

Genetics of Recurrent Vertigo and Vestibular Disorders

Multiomic-based immune response profiling in migraine, vestibular migraine and Meniere's disease

Correction: A systematic review on the contribution of DNA methylation to hearing loss

A systematic review on the contribution of DNA methylation to hearing loss

High prevalence of systemic autoimmune diseases in patients with Menière's disease

Association of a functional polymorphism of PTPN22 encoding a lymphoid protein phosphatase in bilateral Meniere's disease

Epidemiology and genetics of Meniere's disease

Excess of Rare Missense Variants in Hearing Loss Genes in Sporadic Meniere Disease

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