M. Mirrahimi

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.

Prenatal diagnosis of primary congenital glaucoma and histopathological features in a fetal globe with cytochrome p4501B1 mutations

E. Elahi, S. Yazdani, M. Hajizadeh, 2021, European journal of ophthalmology.

Effects of intravitreal connective tissue growth factor neutralizing antibody on choroidal neovascular membrane-associated subretinal fibrosis.

H. Ahmadieh, A. Hafezi-Moghadam, N. Daftarian, 2019, Experimental eye research.

A novel PAX6 mutation causes congenital aniridia with or without retinal detachment

H. Ahmadieh, Hamideh Sabbaghi, Fatemeh Suri, 2019, Ophthalmic genetics.

Variable Expressivity of Wolfram Syndrome in a Family with Multiple Affected Subjects

S. Safi, M. Mohammadzadeh, A. Doozandeh, 2021, Journal of ophthalmic & vision research.

Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment

H. Ahmadieh, L. Kuehlewein, T. Haaf, 2021, Human Genetics.

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.

Triple combination of heat, drug and radiation using alginate hydrogel co-loaded with gold nanoparticles and cisplatin for locally synergistic cancer therapy.

C. Moustakis, H. Ghaznavi, A. Shakeri-Zadeh, 2020, International journal of biological macromolecules.

Gold nanoparticles promote a multimodal synergistic cancer therapy strategy by co-delivery of thermo-chemo-radio therapy.

C. Moustakis, H. Ghaznavi, A. Shakeri-Zadeh, 2020, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Multifunctional Theranostic Graphene Oxide Nanoflakes as MR Imaging Agents with Enhanced Photothermal and Radiosensitizing Properties.

J. Bulte, Abolfazl Sarikhani, H. Ghaznavi, 2021, ACS applied bio materials.

Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment

H. Ahmadieh, L. Kuehlewein, T. Haaf, 2021, Human genetics.

Identification of genes involved in glaucoma pathogenesis using combined network analysis and empirical studies.

E. Elahi, Amir Banaei-Esfahani, S. Yazdani, 2019, Human molecular genetics.

Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy

H. Ahmadieh, N. Daftarian, H. Darvish, 2019, Ophthalmic genetics.