Targeted next generation sequencing identified a novel mutation in MYO7A causing Usher syndrome type 1 in an Iranian consanguineous pedigree von Kooshavar, Daniz, Razipour, Masoumeh, Movasat, Morteza, Keramatipour, Mohammad

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Memantine for axonal loss of optic neuritis von Esfahani, Mohammad Riazi, Harandi, Zahra Alami, Movasat, Morteza, Nikdel, Mojgan, Adelpour, Mohsen, Momeni, Arezo, Merat, Hamid, Fard, Masoud Aghsaei

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Homozygosity Mapping and Targeted Sanger Sequencing Identifies Three Novel CRB1 (Crumbs homologue 1) Mutations in Iranian Retinal Degeneration Families von Ghofrani, Mohammad, Yahyaei, Mahin, Brunner, Han G., Cremers, Frans P.M., Movasat, Morteza, Imran Khan, Muhammad, Keramatipour, Mohammad

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Predictive value of visual evoked potentials, relative afferent pupillary defect, and orbital fractures in patients with traumatic optic neuropathy von Tabatabaei, Seyed Ali, Soleimani, Mohammad, Alizadeh, Mahdi, Movasat, Morteza, Mansoori, Mohammad Reza, Alami, Zakieh, Foroutan, Alireza, Joshaghani, Mahmood, Safari, Saeid, Goldiz, Arzhang

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Vitrectomy for Diffuse Refractory Diabetic Macular Edema Associated with a Taut Premacular Posterior Hyaloid von Hooshang Faghihi, Abolghasem Vahedi, Mohammad Riazi, Zahra Alami Harandi, Ali Tabatabaei, Mohammad-Reza Mansouri, Alireza Lashei, Ahmad Mirshahi, Mehdi Nili Ahmadabadi, Reza Karkhaneh, Mohammad-Sadegh Farahvash, Morteza Movasat, Ahmad Javadian

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