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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

398 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Diagnostic fundus autofluorescence patterns in achromatopsia.
Fahim AT, Khan NW, Zahid S, Schachar IH, Branham K, Kohl S, Wissinger B, Elner VM, Heckenlively JR, Jayasundera T. Fahim AT, et al. Am J Ophthalmol. 2013 Dec;156(6):1211-1219.e2. doi: 10.1016/j.ajo.2013.06.033. Epub 2013 Aug 20. Am J Ophthalmol. 2013. PMID: 23972307
Peripheral fundus findings in X-linked retinoschisis.
Fahim AT, Ali N, Blachley T, Michaelides M. Fahim AT, et al. Br J Ophthalmol. 2017 Nov;101(11):1555-1559. doi: 10.1136/bjophthalmol-2016-310110. Epub 2017 Mar 27. Br J Ophthalmol. 2017. PMID: 28348004 Free article.
Double hyperautofluorescent ring on fundus autofluorescence in ABCA4.
Abalem MF, Qian CX, Branham K, Schlegel D, Fahim AT, Khan NW, Heckenlively JR, Jayasundera KT. Abalem MF, et al. Ophthalmic Genet. 2018 Jan-Feb;39(1):87-91. doi: 10.1080/13816810.2017.1335330. Epub 2017 Jul 20. Ophthalmic Genet. 2018. PMID: 28726568 Free PMC article.
Bullous X linked retinoschisis: clinical features and prognosis.
Hinds AM, Fahim A, Moore AT, Wong SC, Michaelides M. Hinds AM, et al. Among authors: fahim a. Br J Ophthalmol. 2018 May;102(5):622-624. doi: 10.1136/bjophthalmol-2017-310593. Epub 2017 Aug 28. Br J Ophthalmol. 2018. PMID: 28848025
Detailed clinical characterisation, unique features and natural history of autosomal recessive RDH12-associated retinal degeneration.
Fahim AT, Bouzia Z, Branham KH, Kumaran N, Vargas ME, Feathers KL, Perera ND, Young K, Khan NW, Heckenlively JR, Webster AR, Pennesi ME, Ali RR, Thompson DA, Michaelides M. Fahim AT, et al. Br J Ophthalmol. 2019 Dec;103(12):1789-1796. doi: 10.1136/bjophthalmol-2018-313580. Epub 2019 Apr 12. Br J Ophthalmol. 2019. PMID: 30979730 Free PMC article.
Development of a Gene Therapy Vector for RDH12-Associated Retinal Dystrophy.
Feathers KL, Jia L, Perera ND, Chen A, Presswalla FK, Khan NW, Fahim AT, Smith AJ, Ali RR, Thompson DA. Feathers KL, et al. Among authors: fahim at. Hum Gene Ther. 2019 Nov;30(11):1325-1335. doi: 10.1089/hum.2019.017. Epub 2019 Aug 5. Hum Gene Ther. 2019. PMID: 31237438 Free PMC article.
X-Chromosome Inactivation Is a Biomarker of Clinical Severity in Female Carriers of RPGR-Associated X-Linked Retinitis Pigmentosa.
Fahim AT, Sullivan LS, Bowne SJ, Jones KD, Wheaton DKH, Khan NW, Heckenlively JR, Jayasundera KT, Branham KH, Andrews CA, Othman MI, Karoukis AJ, Birch DG, Daiger SP. Fahim AT, et al. Ophthalmol Retina. 2020 May;4(5):510-520. doi: 10.1016/j.oret.2019.11.010. Epub 2019 Nov 18. Ophthalmol Retina. 2020. PMID: 31953110 Free PMC article.
398 results