A Family with a High Incidence of Migraine and Vestibular Migraine and a Case of Menière’s Disease

Could ionic regulation disorders explain the overlap between meniere’s disease and migraine?

(2021) R. Teggi et al.   JOURNAL OF VESTIBULAR RESEARCH-EQUILIBRIUM & ORIENTATION

TRPM7 as a Candidate Gene for Vestibular Migraine

(2020) Eun Hye Oh et al.   Frontiers in Neurology

Simultaneous Presentation of Definite Vestibular Migraine and Definite Ménière's Disease: Overlapping Syndrome of Two Diseases

(2018) Toshihisa Murofushi et al.   Frontiers in Neurology

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

(2017) Roberto Teggi et al.   HEADACHE

A novel missense variant inPRKCBsegregates low-frequency hearing loss in an autosomal dominant family with Meniere’s disease

(2016) Carmen Martín-Sierra et al.   HUMAN MOLECULAR GENETICS

Genetics of vestibular disorders: pathophysiological insights

(2016) Lidia Frejo et al.   JOURNAL OF NEUROLOGY

Clinical Subgroups in Bilateral Meniere Disease

(2016) Lidia Frejo et al.   Frontiers in Neurology

Infantile nystagmus syndrome: clinical characteristics, current theories of pathogenesis, diagnosis, and management

(2015) Michael D. Richards et al.   CANADIAN JOURNAL OF OPHTHALMOLOGY-JOURNAL CANADIEN D OPHTALMOLOGIE

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

(2014) T. Requena et al.   HUMAN MOLECULAR GENETICS

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

(2014) Jose Antonio Lopez-Escamez et al.   Frontiers in Neurology

Familial Clustering of Migraine, Episodic Vertigo, and Ménière's Disease

(2009) Yoon-Hee Cha et al.   OTOLOGY & NEUROTOLOGY