Surgical outcome in class 4 congenital anomalies of the ossicular chain: a systematic review of the literature von Henkemans, S. E, Rovers, J, Thomeer, H. G.X.M

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Surgical decision-making in superior canal dehiscence syndrome with concomitant otosclerosis von Van Dijk, S. W, Peters, J. P.M, Stokroos, R. J, Thomeer, H. G.X.M

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Surgical outcome in class 4 congenital anomalies of the ossicular chain: a systematic review of the literature von Henkemans, S. E., Rovers, J., Thomeer, H. G. X. M.

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Surgical decision-making in superior canal dehiscence syndrome with concomitant otosclerosis von Van Dijk, S. W., Peters, J. P. M., Stokroos, R. J., Thomeer, H. G. X. M.

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Anatomic Malformations of the Middle and Inner Ear in 22q11.2 Deletion Syndrome: Case Series and Literature Review von Verheij, E, Elden, L, Crowley, T B, Pameijer, F A, Zackai, E H, McDonald-McGinn, D M, Thomeer, H G X M

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Prevalence of hearing loss and clinical otologic manifestations in patients with 22q11.2 deletion syndrome: A literature review von Verheij, E., Derks, L.S.M., Stegeman, I., Thomeer, H.G.X.M.

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Ear and hearing problems in relation to karyotype in children with Turner syndrome von Verver, E.J.J., Freriks, K., Thomeer, H.G.X.M., Huygen, P.L.M., Pennings, R.J.E., Alfen-van der Velden, A.A.E.M., Timmers, H.J., Otten, B.J., Cremers, C.W.R.J., Kunst, H.P.M.

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Otological aspects and surgical outcome in a consanguineous family with a novel ANKH gene mutation von Thomeer, H.G.X.M, Morava, E, Verbist, B.M, Cremers, C.W.R.J

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Otologic and audiologic findings in 22q11.2 deletion syndrome von Verheij, E., Kist, A. L., Mink van der Molen, A. B., Stegeman, I., van Zanten, G. A., Grolman, W., Thomeer, H. G. X. M.

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Postoperative headache after surgical treatment of cerebellopontine angle tumors: a systematic review von Pogoda, Louis, Nijdam, Jelle S., Smeeing, Diederik P. J., Voormolen, Eduard H. J., Ziylan, Fuat, Thomeer, Hans G. X. M.

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Stable benefits of bilateral over unilateral cochlear implantation after two years: A randomized controlled trial von van Zon, Alice, Smulders, Yvette E., Stegeman, Inge, Ramakers, Geerte G. J., Kraaijenga, Veronique J. C., Koenraads, Simone P. C., Zanten, Gijsbert A. Van, Rinia, Albert B., Stokroos, Robert J., Free, Rolien H., Frijns, Johan H. M., Huinck, Wendy J., Mylanus, Emmanuel A. M., Tange, Rinze A., Smit, Adriana L., Thomeer, Hans G. X. M., Topsakal, Vedat, Grolman, Wilko

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Clinical Presentation and the Presence of Hearing Impairment in Branchio-Oculo-Facial Syndrome: A New Mutation in the TFAP2A Gene von Thomeer, Henricus G. X. M., Crins, Tom T. H., Kamsteeg, Erik J., Buijsman, Wendy, Cruysberg, Johannes R. M., Knoers, Nine V. A. M., Cremers, W. R. J.

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