Bi-allelic inactivating variants in the COCH gene cause autosomal recessive prelingual hearing impairment von JanssensdeVarebeke, Sebastien P F, Van Camp, Guy, Peeters, Nils, Elinck, Ellen, Widdershoven, Josine, Cox, Tony, Deben, Kristof, Ketelslagers, Katrien, Crins, Tom, Wuyts, Wim

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Focal Sclerosis of Semicircular Canals With Severe DFNA9 Hearing Impairment Caused by a P51S COCH-Mutation: Is There a Link? von de Varebeke, Sebastien Pierre Janssens, Termote, Bruno, Van Camp, Guy, Govaerts, Paul J, Schepers, Steven, Cox, Tony, Deben, Kristof, Ketelslagers, Katrien, Souverijns, Geert

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Results, Hearing Rehabilitation, and Follow-up with Magnetic Resonance Imaging after Tympanomastoid Exenteration, Obliteration, and External Canal Overclosure for Severe Chronic Ot... von Ketelslagers, Katrien, Somers, Thomas, De Foer, Bert, Zarowski, Andrzej, Offeciers, Erwin

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