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M Hamdani

Showing results (11-20 of 32) with videos related to

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Journal Francais D'Ophtalmologie|January 8, 2003
[Ocular impairment during type II membranoproliferative glomerulonephritis]D Lahbil, L Rais, M Hamdani, et al.
IEEE Transactions on Neural Networks and Learning Systems|January 25, 2019
Morphological Convolutional Neural Network Architecture for Digit RecognitionDorra Mellouli, Tarek M Hamdani, Javier J Sanchez-Medina, et al.
Bulletin De La Societe Belge D'Ophtalmologie|November 19, 2003
[Involvement of the optic nerve in the course of Behcet's disease (presentation of 148 cases)]H Lamari, Ali T Baha, M Benhaddou, et al.
Revue De Laryngologie - Otologie - Rhinologie|January 1, 1996
[Goldenhar syndrome: apropos of a case]M D'Khissy, M El Belhadji, M Hamdani, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|September 26, 1997
Unusual scotomas after transsphenoidal surgery of a pituitary macroadenomaH Dollfus, S Gomberg, P Touraine, 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|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 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Journal Francais D'Ophtalmologie|January 8, 2003
[Ocular impairment during type II membranoproliferative glomerulonephritis]D Lahbil, L Rais, M Hamdani, et al.
IEEE Transactions on Neural Networks and Learning Systems|January 25, 2019
Morphological Convolutional Neural Network Architecture for Digit RecognitionDorra Mellouli, Tarek M Hamdani, Javier J Sanchez-Medina, et al.
Bulletin De La Societe Belge D'Ophtalmologie|November 19, 2003
[Involvement of the optic nerve in the course of Behcet's disease (presentation of 148 cases)]H Lamari, Ali T Baha, M Benhaddou, et al.
Revue De Laryngologie - Otologie - Rhinologie|January 1, 1996
[Goldenhar syndrome: apropos of a case]M D'Khissy, M El Belhadji, M Hamdani, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|September 26, 1997
Unusual scotomas after transsphenoidal surgery of a pituitary macroadenomaH Dollfus, S Gomberg, P Touraine, 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|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 4