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Towards personalized medicine in Ménière’s disease

Towards personalized medicine in Ménière’s disease

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_1ac85971b97a41ca8c6391edea20233b

Towards personalized medicine in Ménière’s disease

About this item

Full title

Towards personalized medicine in Ménière’s disease

Publisher

England: Faculty of 1000 Ltd

Journal title

F1000 research, 2018, Vol.7, p.1295

Language

English

Formats

Publication information

Publisher

England: Faculty of 1000 Ltd

More information

Scope and Contents

Contents

Ménière’s disease (MD) represents a heterogeneous group of relatively rare disorders with three core symptoms: episodic vertigo, tinnitus, and sensorineural hearing loss involving 125 to 2,000 Hz frequencies. The majority of cases are considered sporadic, although familial aggregation has been recognized in European and Korean populations, and the...

Alternative Titles

Full title

Towards personalized medicine in Ménière’s disease

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_1ac85971b97a41ca8c6391edea20233b

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_1ac85971b97a41ca8c6391edea20233b

Other Identifiers

ISSN

2046-1402

E-ISSN

2046-1402

DOI

10.12688/f1000research.14417.1

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