1. A novel PAX6 mutation causes congenital aniridia with or without retinal detachment. (4th March 2019) Authors: Mirrahimi, Mehraban; Sabbaghi, Hamideh; Ahmadieh, Hamid; Jahanmard, Mehdi; Hassanpour, Kiana; Suri, Fatemeh Journal: Ophthalmic genetics Issue: Volume 40:Number 2(2019) Page Start: 146 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Association of Saitohin gene rs62063857 polymorphism with dry type age-related macular degeneration. (2nd September 2020) Authors: Bonyadi, Mortaza; Ahmadieh, Hamid; Jabbarpoor Bonyadi, Mohammad Hossein; Shahpasand, Koorosh; Suri, Fatemeh; Nasrabadi, Niyousha; Yaseri, Mehdi; Kheiri, Bahare; Soheilian, Masoud Journal: Ophthalmic genetics Issue: Volume 41:Number 5(2020) Page Start: 505 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Autosomal Recessive Bestrophinopathy: Clinical and Genetic Characteristics of Twenty-Four Cases. (30th April 2021) Authors: Khojasteh, Hassan; Azarmina, Mohsen; Ebrahimiadib, Nazanin; Daftarian, Narsis; Riazi-Esfahani, Hamid; Naraghi, Houra; Sabbaghi, Hamideh; Khodabande, Alireza; Faghihi, Hooshang; Moghaddasi, Afrooz; Bazvand, Fatemeh; Manaviat, Masoud Reza; Ahmadieh, Hamid; Hassanpoor, Narges; Suri, Fatemeh Other Names: Meduri Alessandro Academic Editor. Journal: Journal of ophthalmology Issue: Volume 2021(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. COL18A1 is a candidate eye iridocorneal angle-closure gene in humans. (11th July 2018) Authors: Suri, Fatemeh; Yazdani, Shahin; Chapi, Marjan; Safari, Iman; Rasooli, Paniz; Daftarian, Narsis; Jafarinasab, Mohammad Reza; Ghasemi Firouzabadi, Saghar; Alehabib, Elham; Darvish, Hossein; Klotzle, Brandy; Fan, Jian-Bing; Turk, Casey; Elahi, Elahe Journal: Human molecular genetics Issue: Volume 27:Number 21(2018:Nov. 01) Page Start: 3772 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Effects of intravitreal connective tissue growth factor neutralizing antibody on choroidal neovascular membrane-associated subretinal fibrosis. (July 2019) Authors: Daftarian, Narsis; Rohani, Shirin; Kanavi, Mozhgan Rezaei; Suri, Fatemeh; Mirrahimi, Mehraban; Hafezi-Moghadam, Ali; Soheili, Zahra-Soheila; Ahmadieh, Hamid Journal: Experimental eye research Issue: Volume 184(2019) Page Start: 286 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic screening of TGFBI in Iranian patients with TGFBI-associated corneal dystrophies and a meta-analysis of global variation frequencies. (4th July 2022) Authors: Jozaei, Roxanne; Javadi, Mohammad-Ali; Safari, Iman; Moghaddasi, Afrooz; Feizi, Sepehr; Kanavi, Mozhgan Rezaei; Najafi, Sajad; Safdari, Bahareh; Salahshourifar, Iman; Elahi, Elahe; Suri, Fatemeh Journal: Ophthalmic genetics Issue: Volume 43:Number 4(2022) Page Start: 496 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy. (4th May 2019) Authors: Chapi, Marjan; Sabbaghi, Hamideh; Suri, Fatemeh; Alehabib, Elham; Rahimi-Aliabadi, Simin; Jamali, Faezeh; Jamshidi, Javad; Emamalizadeh, Babak; Darvish, Hossein; Mirrahimi, Mehraban; Ahmadieh, Hamid; Daftarian, Narsis Journal: Ophthalmic genetics Issue: Volume 40:Number 3(2019) Page Start: 259 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Intravitreal connective tissue growth factor neutralizing antibody or bevacizumab alone or in combination for prevention of proliferative vitreoretinopathy in an experimental model. (July 2021) Authors: Daftarian, Narsis; Baigy, Omolbanin; Suri, Fatemeh; Kanavi, Mozhgan Rezaei; Balagholi, Sahar; Afsar Aski, Sasha; Moghaddasi, Afrooz; Nourinia, Ramin; Abtahi, Seyed-Hossein; Ahmadieh, Hamid Journal: Experimental eye research Issue: Volume 208(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Prenatal diagnosis of primary congenital glaucoma and histopathological features in a fetal globe with cytochrome p4501B1 mutations. Issue 2 (March 2022) Authors: Rezaei Kanavi, Mozhgan; Yazdani, Shahin; Elahi, Elahe; Mirrahimi, Mehraban; Hajizadeh, Maryam; Khodaverdi, Sepideh; Suri, Fatemeh Journal: European journal of ophthalmology Issue: Volume 32:Issue 2(2022) Page Start: 933 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗