Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

70 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy.
Chapi M, Sabbaghi H, Suri F, Alehabib E, Rahimi-Aliabadi S, Jamali F, Jamshidi J, Emamalizadeh B, Darvish H, Mirrahimi M, Ahmadieh H, Daftarian N. Chapi M, et al. Among authors: sabbaghi h. Ophthalmic Genet. 2019 Jun;40(3):259-266. doi: 10.1080/13816810.2019.1622023. Epub 2019 Jun 19. Ophthalmic Genet. 2019. PMID: 31215831
The First Inherited Retinal Disease Registry in Iran: Research Protocol and Results of a Pilot Study.
Sabbaghi H, Daftarian N, Suri F, Mirrahimi M, Madani S, Sheikhtaheri A, Khorrami F, Saviz P, Zarei Nejad M, Tivay A, Shahriari HA, Maleki A, Ahmadi SS, Sargazi M, Cremers FPM, Najafi M, Vona B, Haaf T, Bahena-Carbajal P, Moghadasi A, Naraghi H, Yaseri M, Kheiri B, Kalantarion M, Sabbaghi E, Salami M, Pazooki L, Zendedel K, Mojarrab S, Ahmadieh H. Sabbaghi H, et al. Among authors: sabbaghi e. Arch Iran Med. 2020 Jul 1;23(7):445-454. doi: 10.34172/aim.2020.41. Arch Iran Med. 2020. PMID: 32657595 Free article.
Choroidal Thickness in Different Types of Inherited Retinal Dystrophies.
Sabbaghi H, Ahmadieh H, Jalili J, Behnaz N, Fakhri M, Suri F, Kheiri B, Rajabpour M, Entezari M, Daftarian N. Sabbaghi H, et al. J Ophthalmic Vis Res. 2020 Aug 6;15(3):351-361. doi: 10.18502/jovr.v15i3.7454. eCollection 2020 Jul-Sep. J Ophthalmic Vis Res. 2020. PMID: 32864066 Free PMC article. Review.
Autosomal Recessive Bestrophinopathy: Clinical and Genetic Characteristics of Twenty-Four Cases.
Khojasteh H, Azarmina M, Ebrahimiadib N, Daftarian N, Riazi-Esfahani H, Naraghi H, Sabbaghi H, Khodabande A, Faghihi H, Moghaddasi A, Bazvand F, Manaviat MR, Ahmadieh H, Hassanpoor N, Suri F. Khojasteh H, et al. Among authors: sabbaghi h. J Ophthalmol. 2021 Apr 30;2021:6674290. doi: 10.1155/2021/6674290. eCollection 2021. J Ophthalmol. 2021. PMID: 34012682 Free PMC article.
70 results