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Clinical Genetics|October 10, 2002
A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in MoroccoA Belmouden, R Melki, M Hamdani, et al.Journal Francais D'Ophtalmologie|October 18, 2000
[Gyrate atrophy of the choroid and retina: a case report]D Lahbil, M Hamdani, M D'khissy, et al.Bulletin De La Societe Belge D'Ophtalmologie|April 27, 2005
[Apert syndrome: a reported observation]S Dihaj, A Abada, T Baha Ali, et al.Journal Francais D'Ophtalmologie|November 27, 2013
[Pseudophakic retinal detachment: how to manage?]L Benhmidoune, Y Elkharroubi, A A Bensemlali, et al.Neuro-Chirurgie|June 8, 2002
[Subperiosteal hematoma of the orbit associated with subfrontal extradural hematoma]A Naja, A Chellaoui, K Ibahioin, et al.Journal Francais D'Ophtalmologie|March 9, 2006
[Fraser syndrome. A case report]B Allali, M Hamdani, H Lamari, et al.Journal Francais D'Ophtalmologie|October 18, 2000
[Juvenile xanthogranuloma with intraocular involvement. A case report]M Hamdani, A El Kettani, L Rais, et al.Journal Francais D'Ophtalmologie|October 23, 2004
[A case of a retinitis pigmentosa and asteroid hyalosis]M Wafi, L Raïs, D Lahbil, et al.Annales De Dermatologie Et De Venereologie|May 11, 2000
[Vogt-Koyanagi-Harada's disease: 3 cases]O Mikou, S Chiheb, K Zouhair, et al.Journal Francais D'Ophtalmologie|March 27, 2002
[Weill Marchesani syndrome. Report of a case]A el Kettani, M Hamdani, L Rais, et al.Pageof 6