Ihab Saad

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H. Abouzeid, I. S. Othman and D. F. Schorderet, 2016, A Novel Recessive RPGRIP1 Mutation Causing Leber Congenital Amaurosis, Klin Monbl Augenheilkd, 233, 456-9

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and H. Abouzeid, O. S. I. S. D. F., H. Abouzeid, I. S. Othman and D. F. Schorderet, 2016, A Novel Recessive RPGRIP1 Mutation Causing Leber Congenital Amaurosis, Klin Monbl Augenheilkd, 233, 456-9, , 2016.
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Recent Publications

H. Abouzeid, I. S. Othman and D. F. Schorderet, 2016, A Novel Recessive RPGRIP1 Mutation Causing Leber Congenital Amaurosis, Klin Monbl Augenheilkd, 233, 456-9
H. Abouzeid, I. S. Othman and D. F. Schorderet, 2016, A Novel Recessive RPGRIP1 Mutation Causing Leber Congenital Amaurosis, Klin Monbl Augenheilkd, 233, 456-9
C. Jakobsson, I. S. Othman, F. L. Munier, D. F. Schorderet and H. Abouzeid, 2014, Cone-rod dystrophy caused by a novel homozygous RPE65 mutation in Leber congenital amaurosis, Klin Monbl Augenheilkd, 231, 405-10
I. S. Othman, S. A. Eissa, M. S. Kotb and S. H. Sadek, 2014, Subthreshold diode-laser micropulse photocoagulation as a primary and secondary line of treatment in management of diabetic macular edema, Clin Ophthalmol, 8, 653-9
I. S. Othman, M. Assem and I. M. Zaki, 2013, Secondary glaucoma as initial manifestation of uveal melanoma, Saudi J Ophthalmol, 27, 203-8
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