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Predictive value of visual evoked potentials, relative afferent pupillary defect, and orbital fractures in patients with traumatic optic neuropathy.
Clin Ophthalmol. 2011;5:1021-6. doi: 10.2147/OPTH.S21409. Epub 2011 Jul 25.
Clin Ophthalmol. 2011.
PMID: 21845028
Free PMC article.
Memantine for axonal loss of optic neuritis.
Esfahani MR, Harandi ZA, Movasat M, Nikdel M, Adelpour M, Momeni A, Merat H, Fard MA.
Esfahani MR, et al. Among authors: movasat m.
Graefes Arch Clin Exp Ophthalmol. 2012 Jun;250(6):863-9. doi: 10.1007/s00417-011-1894-3. Epub 2011 Dec 16.
Graefes Arch Clin Exp Ophthalmol. 2012.
PMID: 22173217
Clinical Trial.
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Homozygosity Mapping and Targeted Sanger Sequencing Identifies Three Novel CRB1 (Crumbs homologue 1) Mutations in Iranian Retinal Degeneration Families.
Ghofrani M, Yahyaei M, Brunner HG, Cremers FP, Movasat M, Imran Khan M, Keramatipour M.
Ghofrani M, et al. Among authors: movasat m.
Iran Biomed J. 2017 Sep;21(5):294-302. doi: 10.18869/acadpub.ibj.21.5.294. Epub 2017 May 2.
Iran Biomed J. 2017.
PMID: 28460491
Free PMC article.
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Targeted next generation sequencing identified a novel mutation in MYO7A causing Usher syndrome type 1 in an Iranian consanguineous pedigree.
Kooshavar D, Razipour M, Movasat M, Keramatipour M.
Kooshavar D, et al. Among authors: movasat m.
Int J Pediatr Otorhinolaryngol. 2018 Jan;104:10-13. doi: 10.1016/j.ijporl.2017.10.022. Epub 2017 Oct 18.
Int J Pediatr Otorhinolaryngol. 2018.
PMID: 29287847
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