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Page 1
Similar phenotypes caused by mutations in OTOG and OTOGL.
Oonk AM, Leijendeckers JM, Huygen PL, Schraders M, del Campo M, del Castillo I, Tekin M, Feenstra I, Beynon AJ, Kunst HP, Snik AF, Kremer H, Admiraal RJ, Pennings RJ. Oonk AM, et al. Among authors: admiraal rj. Ear Hear. 2014 May-Jun;35(3):e84-91. doi: 10.1097/AUD.0000000000000008. Ear Hear. 2014. PMID: 24378291 Free PMC article.
Paediatric Cochlear Implantation in Patients with Waardenburg Syndrome.
van Nierop JW, Snabel RR, Langereis M, Pennings RJ, Admiraal RJ, Mylanus EA, Kunst HP. van Nierop JW, et al. Among authors: admiraal rj. Audiol Neurootol. 2016;21(3):187-94. doi: 10.1159/000444120. Epub 2016 Jun 1. Audiol Neurootol. 2016. PMID: 27245679 Free PMC article.
Hearing impairment in Stickler syndrome.
Admiraal RJ, Szymko YM, Griffith AJ, Brunner HG, Huygen PL. Admiraal RJ, et al. Adv Otorhinolaryngol. 2002;61:216-23. doi: 10.1159/000066812. Adv Otorhinolaryngol. 2002. PMID: 12408087 Review. No abstract available.
Vestibular function and temporal bone imaging in DFNB1.
Oonk AM, Beynon AJ, Peters TA, Kunst HP, Admiraal RJ, Kremer H, Verbist B, Pennings RJ. Oonk AM, et al. Among authors: admiraal rj. Hear Res. 2015 Sep;327:227-34. doi: 10.1016/j.heares.2015.07.009. Epub 2015 Jul 15. Hear Res. 2015. PMID: 26188104
Patients with Pendred syndrome: is cochlear implantation beneficial?
van Nierop JW, Huinck WJ, Pennings RJ, Admiraal RJ, Mylanus EA, Kunst HP. van Nierop JW, et al. Among authors: admiraal rj. Clin Otolaryngol. 2016 Aug;41(4):386-94. doi: 10.1111/coa.12532. Epub 2016 Feb 8. Clin Otolaryngol. 2016. PMID: 26331303
Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophy.
Wesdorp M, Schreur V, Beynon AJ, Oostrik J, van de Kamp JM, Elting MW, van den Boogaard MH, Feenstra I, Admiraal RJC, Kunst HPM, Hoyng CB, Kremer H, Yntema HG, Pennings RJE, Schraders M. Wesdorp M, et al. Among authors: admiraal rjc. Clin Genet. 2018 Aug;94(2):221-231. doi: 10.1111/cge.13368. Epub 2018 Jun 8. Clin Genet. 2018. PMID: 29676012
71 results