Khan NW - Search Results

1

Contrast sensitivity deficits in patients with mutation-proven inherited retinal degenerations.

Alahmadi BO, Omari AA, Abalem MF, Andrews C, Schlegel D, Branham KH, Khan NW, Fahim A, Jayasundera T. Alahmadi BO, et al. Among authors: khan nw. BMC Ophthalmol. 2018 Dec 7;18(1):313. doi: 10.1186/s12886-018-0982-0. BMC Ophthalmol. 2018. PMID: 30526558 Free PMC article.

2

Clinical course and visual function in a family with mutations in the RPE65 gene.

Felius J, Thompson DA, Khan NW, Bingham EL, Jamison JA, Kemp JA, Sieving PA. Felius J, et al. Among authors: khan nw. Arch Ophthalmol. 2002 Jan;120(1):55-61. doi: 10.1001/archopht.120.1.55. Arch Ophthalmol. 2002. PMID: 11786058

3

Nrl-knockout mice deficient in Rpe65 fail to synthesize 11-cis retinal and cone outer segments.

Feathers KL, Lyubarsky AL, Khan NW, Teofilo K, Swaroop A, Williams DS, Pugh EN Jr, Thompson DA. Feathers KL, et al. Among authors: khan nw. Invest Ophthalmol Vis Sci. 2008 Mar;49(3):1126-35. doi: 10.1167/iovs.07-1234. Invest Ophthalmol Vis Sci. 2008. PMID: 18326740 Free PMC article.

4

Management of autoimmune retinopathies with immunosuppression.

Ferreyra HA, Jayasundera T, Khan NW, He S, Lu Y, Heckenlively JR. Ferreyra HA, et al. Among authors: khan nw. Arch Ophthalmol. 2009 Apr;127(4):390-7. doi: 10.1001/archophthalmol.2009.24. Arch Ophthalmol. 2009. PMID: 19365013

5

Establishing baseline rod electroretinogram values in achromatopsia and cone dystrophy.

Wang I, Khan NW, Branham K, Wissinger B, Kohl S, Heckenlively JR. Wang I, et al. Among authors: khan nw. Doc Ophthalmol. 2012 Dec;125(3):229-33. doi: 10.1007/s10633-012-9350-1. Epub 2012 Aug 19. Doc Ophthalmol. 2012. PMID: 22903242

6

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. Among authors: khan nw. 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

7

Acute panretinal structural and functional abnormalities after intravitreous ocriplasmin injection.

Fahim AT, Khan NW, Johnson MW. Fahim AT, et al. Among authors: khan nw. JAMA Ophthalmol. 2014 Apr 1;132(4):484-6. doi: 10.1001/jamaophthalmol.2013.8142. JAMA Ophthalmol. 2014. PMID: 24577241

8

Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium.

Thompson DA, Ali RR, Banin E, Branham KE, Flannery JG, Gamm DM, Hauswirth WW, Heckenlively JR, Iannaccone A, Jayasundera KT, Khan NW, Molday RS, Pennesi ME, Reh TA, Weleber RG, Zacks DN; Monaciano Consortium. Thompson DA, et al. Among authors: khan nw. Invest Ophthalmol Vis Sci. 2015 Feb 9;56(2):918-31. doi: 10.1167/iovs.14-16049. Invest Ophthalmol Vis Sci. 2015. PMID: 25667399 Free PMC article. Review.

9

Expansion of Severely Constricted Visual Field Using Google Glass.

Trese MG, Khan NW, Branham K, Conroy EB, Moroi SE. Trese MG, et al. Among authors: khan nw. Ophthalmic Surg Lasers Imaging Retina. 2016 May 1;47(5):486-9. doi: 10.3928/23258160-20160419-15. Ophthalmic Surg Lasers Imaging Retina. 2016. PMID: 27183556

10

Reliability of kinetic visual field testing in children with mutation-proven retinal dystrophies: Implications for therapeutic clinical trials.

Dedania VS, Liu JY, Schlegel D, Andrews CA, Branham K, Khan NW, Musch DC, Heckenlively JR, Jayasundera KT. Dedania VS, et al. Among authors: khan nw. Ophthalmic Genet. 2018 Jan-Feb;39(1):22-28. doi: 10.1080/13816810.2017.1329447. Epub 2017 Jul 13. Ophthalmic Genet. 2018. PMID: 28704108 Free PMC article.

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