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8. Distinct vestibular phenotypes in DFNA9 families with COCH variants. Kim BJ; Kim AR; Han KH; Rah YC; Hyun J; Ra BS; Koo JW; Choi BY Eur Arch Otorhinolaryngol; 2016 Oct; 273(10):2993-3002. PubMed ID: 26758463 [TBL] [Abstract][Full Text] [Related]
9. Vertical corneal striae in families with autosomal dominant hearing loss: DFNA9/COCH. Bischoff AM; Pauw RJ; Huygen PL; Aandekerk AL; Kremer H; Cremers CW; Cruysberg JR Am J Ophthalmol; 2007 May; 143(5):847-852. PubMed ID: 17368553 [TBL] [Abstract][Full Text] [Related]
10. Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease. Usami S; Takahashi K; Yuge I; Ohtsuka A; Namba A; Abe S; Fransen E; Patthy L; Otting G; Van Camp G Eur J Hum Genet; 2003 Oct; 11(10):744-8. PubMed ID: 14512963 [TBL] [Abstract][Full Text] [Related]
11. The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction? Fransen E; Van Camp G Br J Audiol; 1999 Oct; 33(5):297-302. PubMed ID: 10890144 [TBL] [Abstract][Full Text] [Related]
12. Sensitivity and specificity of vestibular bed-side examination in detecting VIII cranial nerve schwannoma with sensorineural sudden unilateral hearing loss as presenting symptom. Califano L; Salafia F; Melillo MG; Mazzone S Acta Otorhinolaryngol Ital; 2017 Aug; 37(4):336-340. PubMed ID: 28530253 [TBL] [Abstract][Full Text] [Related]
13. Acute vertigo and sensorineural hearing loss from infarction of the vestibulocochlear nerve: A case report. Byun S; Lee JY; Kim BG; Hong HS Medicine (Baltimore); 2018 Oct; 97(41):e12777. PubMed ID: 30313095 [TBL] [Abstract][Full Text] [Related]
14. High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene. Fransen E; Verstreken M; Verhagen WI; Wuyts FL; Huygen PL; D'Haese P; Robertson NG; Morton CC; McGuirt WT; Smith RJ; Declau F; Van de Heyning PH; Van Camp G Hum Mol Genet; 1999 Aug; 8(8):1425-9. PubMed ID: 10400989 [TBL] [Abstract][Full Text] [Related]
15. Cross-sectional analysis of hearing threshold in relation to age in a large family with cochleovestibular impairment thoroughly genotyped for DFNA9/COCH. Bom SJ; Kemperman MH; Huygen PL; Luijendijk MW; Cremers CW Ann Otol Rhinol Laryngol; 2003 Mar; 112(3):280-6. PubMed ID: 12656423 [TBL] [Abstract][Full Text] [Related]
16. [Intralabyrinthine schwannoma of the vestibulocochlear nerve]. Brozek-Madry E; Niemczyk K; Morawski K Otolaryngol Pol; 2009; 63(5):437-41. PubMed ID: 20169910 [TBL] [Abstract][Full Text] [Related]
17. Familial auditory neuropathy. Wang Q; Gu R; Han D; Yang W Laryngoscope; 2003 Sep; 113(9):1623-9. PubMed ID: 12972945 [TBL] [Abstract][Full Text] [Related]
19. A systematic review of hearing and vestibular function in carriers of the Pro51Ser mutation in the COCH gene. JanssensdeVarebeke S; Topsakal V; Van Camp G; Van Rompaey V Eur Arch Otorhinolaryngol; 2019 May; 276(5):1251-1262. PubMed ID: 30806805 [TBL] [Abstract][Full Text] [Related]