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Revue De Laryngologie - Otologie - Rhinologie|January 1, 1996
[Goldenhar syndrome: apropos of a case]M D'Khissy, M El Belhadji, M Hamdani, et al.Presse Medicale (Paris, France : 1983)|October 26, 1996
[Anaphylactic shock caused by application of fluorescein on the ocular conjunctiva]N el Harrar, B Idali, S Moutaouakkil, et al.Annales De Medecine Interne|January 1, 1992
[Ophthalmologic manifestations in patients under chronic hemodialysis]A Bourquia, K Zaghloul, S Berrada, 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.Journal Francais D'Ophtalmologie|February 11, 2014
[Retinoblastoma: preliminary results of national treatment protocol at Casablanca university medical center]A El Kettani, S Aderdour, G Daghouj, et al.Journal Francais D'Ophtalmologie|January 1, 1997
[Bilateral Sturge-Weber-Krabbe syndrome. Apropos of a case]M Hamdani, L Rais, M Elbelhadj, et al.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|March 27, 2002
[Weill Marchesani syndrome. Report of a case]A el Kettani, M Hamdani, L Rais, et al.Pageof 5