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

Headache, 2018-04, Vol.58 (4), p.534-544

2018

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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

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

2015

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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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Genetics of vestibular disorders: pathophysiological insights

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

2016

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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

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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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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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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Genetics of Recurrent Vertigo and Vestibular Disorders

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

2011

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A Systematic Review on Heritability of Sudden Sensorineural Hearing Loss

The Laryngoscope, 2024-01

2024

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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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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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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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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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Application of Human Stem Cells to Model Genetic Sensorineural Hearing Loss and Meniere Disease

Cells (Basel, Switzerland), 2023-03, Vol.12 (7), p.988

2023

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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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Epidemiology and genetics of Meniere's disease

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

2024

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Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study

EBioMedicine, 2021-04, Vol.66, p.103309-103309, Article 103309

2021

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Editorial: Epidemiology and Genetics of Vestibular Disorders

Frontiers in neurology, 2021-09, Vol.12, p.743379-743379

2021

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Standardized Clinical Profiling in Spanish Patients with Chronic Tinnitus

Journal of clinical medicine, 2022-02, Vol.11 (4), p.978

2022

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Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease

PloS one, 2014-11, Vol.9 (11), p.e112171-e112171

2014

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Rare Deletions or Large Duplications Contribute to Genetic Variation in Patients with Severe Tinnitus and Meniere Disease

Genes, 2024-01, Vol.15 (1), p.22

2024

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Genetic architecture of Meniere’s disease

Hearing research, 2020-11, Vol.397, p.107872-107872, Article 107872

2020

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

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

Diagnostic criteria for Menière's disease

A tinnitus symphony in 100 patients with Meniere's disease

Genetics of vestibular disorders: pathophysiological insights

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

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

Types of Inheritance and Genes Associated with Familial Meniere Disease

Genetics of Recurrent Vertigo and Vestibular Disorders

A Systematic Review on Heritability of Sudden Sensorineural Hearing Loss

Systematic Review of Prevalence Studies and Familial Aggregation in Vestibular Migraine

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

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

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

Application of Human Stem Cells to Model Genetic Sensorineural Hearing Loss and Meniere Disease

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

Epidemiology and genetics of Meniere's disease

Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study

Editorial: Epidemiology and Genetics of Vestibular Disorders

Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere's Disease

Standardized Clinical Profiling in Spanish Patients with Chronic Tinnitus

Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease

Rare Deletions or Large Duplications Contribute to Genetic Variation in Patients with Severe Tinnitus and Meniere Disease

Genetic architecture of Meniere’s disease

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