Afrooz Moghadasi

The First Inherited Retinal Disease Registry in Iran: Research Protocol and Results of a Pilot Study.

H. Ahmadieh, M. Yaseri, F. Cremers, 2020, Archives of Iranian medicine.

PRPH2 mutation as the cause of various clinical manifestations in a family affected with inherited retinal dystrophy

H. Ahmadieh, N. Daftarian, Hamideh Sabbaghi, 2019, Ophthalmic genetics.