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Items: 1 to 20 of 37

1.

Improving the visual outcome in Leber's hereditary optic neuropathy: Framework for the future.

Asanad S, Frousiakis S, Wang MY, Fantini M, Sultan W, Wood T, Nwako FU, Karanjia R, Sadun AA.

J Curr Ophthalmol. 2019 Jun 6;31(3):251-253. doi: 10.1016/j.joco.2019.05.004. eCollection 2019 Sep. No abstract available.

2.

Long-term attenuation of the deep capillary plexus in SLE utilizing OCTA.

Sultan W, Asanad S, Karanjia R, Sadun AA.

Can J Ophthalmol. 2019 Aug;54(4):e207-e212. doi: 10.1016/j.jcjo.2018.10.013. Epub 2019 Jan 14. No abstract available.

PMID:
31358173
3.

The Retina in Alzheimer's Disease: Histomorphometric Analysis of an Ophthalmologic Biomarker.

Asanad S, Ross-Cisneros FN, Nassisi M, Barron E, Karanjia R, Sadun AA.

Invest Ophthalmol Vis Sci. 2019 Apr 1;60(5):1491-1500. doi: 10.1167/iovs.18-25966.

PMID:
30973577
4.

Hormone replacement therapy in Leber's hereditary optic neuropathy: Accelerated visual recovery in vivo.

Fantini M, Asanad S, Karanjia R, Sadun A.

J Curr Ophthalmol. 2018 Nov 3;31(1):102-105. doi: 10.1016/j.joco.2018.10.003. eCollection 2019 Mar.

5.

Endovascular Stenting in a Transgender Patient With Idiopathic Intracranial Hypertension.

Kogachi K, Konstas A, Karanjia R, Sadun AA.

J Neuroophthalmol. 2019 Jun;39(2):247-248. doi: 10.1097/WNO.0000000000000752. No abstract available.

PMID:
30844882
6.

Optical Coherence Tomography of the Retinal Ganglion Cell Complex in Leber's Hereditary Optic Neuropathy and Dominant Optic Atrophy.

Asanad S, Tian JJ, Frousiakis S, Jiang JP, Kogachi K, Felix CM, Fatemeh D, Irvine AG, Ter-Zakarian A, Falavarjani KG, Barboni P, Karanjia R, Sadun AA.

Curr Eye Res. 2019 Jun;44(6):638-644. doi: 10.1080/02713683.2019.1567792. Epub 2019 Feb 4.

PMID:
30649972
7.

Value of medical history in ophthalmology: A study of diagnostic accuracy.

Wang MY, Asanad S, Asanad K, Karanjia R, Sadun AA.

J Curr Ophthalmol. 2018 Sep 27;30(4):359-364. doi: 10.1016/j.joco.2018.09.001. eCollection 2018 Dec.

8.

Unilateral cone-rod dysfunction and retinal thinning in a child carrying the 14484 mutation of Leber hereditary optic neuropathy.

Kassem A, Karanjia R, McClelland C, Sadun A, Lee MS.

J AAPOS. 2019 Apr;23(2):104-106. doi: 10.1016/j.jaapos.2018.09.005. Epub 2018 Nov 14.

PMID:
30447424
9.

Toxic medications in Leber's hereditary optic neuropathy.

Kogachi K, Ter-Zakarian A, Asanad S, Sadun A, Karanjia R.

Mitochondrion. 2019 May;46:270-277. doi: 10.1016/j.mito.2018.07.007. Epub 2018 Aug 4. Review.

PMID:
30081212
10.

Management of ophthalmologic manifestations of mitochondrial diseases.

Newman NJ, Yu-Wai-Man P, Sadun AA, Karanjia R, Carelli V.

Genet Med. 2017 Dec;19(12). doi: 10.1038/gim.2017.171. Epub 2017 Oct 26. No abstract available.

PMID:
29215643
11.

The Photopic Negative Response: An Objective Measure of Retinal Ganglion Cell Function in Patients With Leber's Hereditary Optic Neuropathy.

Karanjia R, Berezovsky A, Sacai PY, Cavascan NN, Liu HY, Nazarali S, Moraes-Filho MN, Anderson K, Tran JS, Watanabe SE, Moraes MN, Sadun F, DeNegri AM, Barboni P, do Val Ferreira Ramos C, La Morgia C, Carelli V, Belfort R Jr, Coupland SG, Salomao SR, Sadun AA.

Invest Ophthalmol Vis Sci. 2017 May 1;58(6):BIO300-BIO306. doi: 10.1167/iovs.17-21773.

PMID:
29049835
12.

Melanoma-Associated Retinopathy 28 Years After Diagnosis.

Tian JJ, Coupland S, Karanjia R, Sadun AA.

JAMA Ophthalmol. 2017 Nov 1;135(11):1276-1277. doi: 10.1001/jamaophthalmol.2017.3500. No abstract available.

13.

Validity of Forced Eyelid Closure Test: A Novel Clinical Screening Test for Ocular Myasthenia Gravis.

Apinyawasisuk S, Zhou X, Tian JJ, Garcia GA, Karanjia R, Sadun AA.

J Neuroophthalmol. 2017 Sep;37(3):253-257. doi: 10.1097/WNO.0000000000000514.

14.

Profound vision loss impairs psychological well-being in young and middle-aged individuals.

Garcia GA, Khoshnevis M, Gale J, Frousiakis SE, Hwang TJ, Poincenot L, Karanjia R, Baron D, Sadun AA.

Clin Ophthalmol. 2017 Feb 22;11:417-427. doi: 10.2147/OPTH.S113414. eCollection 2017.

15.

Corneal etching in femtosecond laser-assisted cataract surgery.

Garcia GA, Tian JJ, Falavarjani KG, Karanjia R, Lu KL.

Can J Ophthalmol. 2017 Feb;52(1):e15-e18. doi: 10.1016/j.jcjo.2016.07.010. Epub 2017 Jan 4. No abstract available.

PMID:
28237162
16.

Natural History of Conversion of Leber's Hereditary Optic Neuropathy: A Prospective Case Series.

Hwang TJ, Karanjia R, Moraes-Filho MN, Gale J, Tran JS, Chu ER, Salomao SR, Berezovsky A, Belfort R Jr, Moraes MN, Sadun F, DeNegri AM, La Morgia C, Barboni P, Ramos CDVF, Chicani CF, Quiros PA, Carelli V, Sadun AA.

Ophthalmology. 2017 Jun;124(6):843-850. doi: 10.1016/j.ophtha.2017.01.002. Epub 2017 Feb 10.

PMID:
28196731
17.

Treatment of Leber's Hereditary Optic Neuropathy.

Karanjia R, Chahal J, Ammar M, Sadun AA.

Curr Pharm Des. 2017;23(4):624-628. doi: 10.2174/1381612823666170125164856. Review.

PMID:
28128056
18.

High Rate of Early Posterior Capsule Opacification following Femtosecond Laser-Assisted Cataract Surgery.

Rostami B, Tian J, Jackson N, Karanjia R, Lu K.

Case Rep Ophthalmol. 2016 Oct 11;7(3):213-217. doi: 10.1159/000449124. eCollection 2016 Sep-Dec.

19.

Hepatic steatosis and fibrosis: Non-invasive assessment.

Karanjia RN, Crossey MM, Cox IJ, Fye HK, Njie R, Goldin RD, Taylor-Robinson SD.

World J Gastroenterol. 2016 Dec 7;22(45):9880-9897. doi: 10.3748/wjg.v22.i45.9880. Review.

20.

A method for identifying color vision deficiency malingering.

Pouw A, Karanjia R, Sadun A.

Graefes Arch Clin Exp Ophthalmol. 2017 Mar;255(3):613-618. doi: 10.1007/s00417-016-3570-0. Epub 2016 Dec 21.

PMID:
28004196

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