Autologous peripheral retinal pigment epithelium translocation in patients with subfoveal neovascular membranes von van Meurs, J C, ter Averst, E, Hofland, L J, van Hagen, P M, Mooy, C M, Baarsma, G S, Kuijpers, R W, Boks, T, Stalmans, P

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Comments on 'Clinical and cytopathologic correlation in chronic inflammations of the orbit and ocular adnexa: A review of 55 cases' by Upreet Dhaliwal et al von PhD, C.M. Mooy MD

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2256 A solid, unilateral equatorial intraocular tumor von De Jong, P.T.V.M., Mooy, C.M.

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Neural cell adhesion molecule distribution in primary and metastatic uveal melanoma von Mooy, C.M, Luyten, G.P.M, de Jong, P.T.V.M, Jensen, O.A, Luider, T.M, van der Ham, F, Bosman, F.T

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A Chicken Embryo Model to Study the Growth of Human Uveal Melanoma von Luyten, G.P.M., Mooy, C.M., Dejong, P.T.V.M., Hoogeveen, A.T., Luider, T.M.

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Syringomateus Carcinoma of the eyelid ans orbit: a clinical and histopathological challenge von Hoppenreijs, V.P.T, Reuser, T.T.Q, Mooy, C.M, de Keizer, R.J.W, Mourits, M.P

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Perinatally ruptured dermoid cyst presenting as congenital oculomotor palsy von Coevoet, H.M.N., van Minderhout, H.M., Mooy, C.M., Simonsz, H.J.

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4124 Identification of glycosaminoglycans in age-related macular deposits von Kliffen, M., Huijmans, J.G.M., Mooy, C.M., Luider, T.M., Kerkvliet, S., De Jong, P.T.V.M.

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Ki-67 immunostaining in uveal melanoma: the effect of pre-enucleation radiotherapy von MOOY, C. M, DE JONG, P. T. V. M, VAN DER KWAST, MULDER, P. G. H, JAGER, M. J, RUITER, D. J

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Perinatally ruptured dermoid cyst presenting as congenital oculomotor palsy von Coevoet, H.M.N., van Minderhout, H.M., Mooy, C.M., Simonsz, H.J.

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Immune Deposits in Iris Biopsy Specimens From Patients With Fuchs' Heterochromic Iridocyclitis von de Jong, P.T.V.M., La Hey, E., Mooy, C.M., Baarsma, G.S., de Vries, J., Kijlstra, A.

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Immunohistochemical Analysis of Iris Biopsy Specimens From Patients With Fuchs' Heterochromic Cyclitis von Murray, P.I., Mooy, C.M., Visser-de Jong, E., Baarsma, G.S., de Vries, J., de Jong, P.T.V.M., Kijlstra, A.

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Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations von Petrij, Fred, Dauwerse, Hans G, Blough, Ruthann I, Giles, Rachel H, van der Smagt, Jasper J, Wallerstein, Robert, Maaswinkel-Mooy, Petra D, van Karnebeek, Clara D, van Ommen, Gert-Jan B, van Haeringen, Arie, Rubinstein, Jack H, Saal, Howard M, Hennekam, Raoul C M, Peters, Dorien J M, Breuning, Martijn H

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Oculoauriculovertebral spectrum and cerebral anomalies von Schrander-Stumpel, C T, de Die-Smulders, C E, Hennekam, R C, Fryns, J P, Bouckaert, P X, Brouwer, O F, da Costa, J J, Lommen, E J, Maaswinkel-Mooy, P D

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Congenital glaucoma in a child with partial lq duplication and 9p deletion von Verbraak, Frank D., Pogány, Katalin, Pilon, Jan-Willem, Mooy, C. m., De France, H. F., Hennekam, Raoul C.m., Bleeker-Wagemakers, E. M.

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