Clinical and genetic significance of unilateral Lisch nodules
Ceuterick, S D, Van Den Ende, J J, Smets, R M E
Published in Bulletin de la Société Belge d'Ophtalmologie (2005)
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Published in Bulletin de la Société Belge d'Ophtalmologie (2005)
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Hereditary otovestibular dysfunction and Ménière's disease in a large Belgian family is caused by a missense mutation in the COCH gene
Verstreken, M, Declau, F, Wuyts, F L, D'Haese, P, Van Camp, G, Fransen, E, Van den Hauwe, L, Buyle, S, Smets, R E, Feenstra, L, Van der Stappen, A, Van de Heyning, P H
Published in Otology & neurotology (01.11.2001)
Published in Otology & neurotology (01.11.2001)
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Secondary closure of posterior continuous curvilinear capsulorhexis
Tassignon, M.J., De Groot, V., Smets, R.M.E., Tawab, B., Vervecken, F.
Published in Journal of cataract and refractive surgery (01.11.1996)
Published in Journal of cataract and refractive surgery (01.11.1996)
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