504 related articles for article (PubMed ID: 27631475)
1. Macular Retinal Sublayer Thicknesses in G11778A Leber Hereditary Optic Neuropathy.
Lam BL; Burke SP; Wang MX; Nadayil GA; Rosa PR; Gregori G; Feuer WJ; Cuprill-Nilson S; Vandenbroucke R; Zhang X; Guy J
Ophthalmic Surg Lasers Imaging Retina; 2016 Sep; 47(9):802-10. PubMed ID: 27631475
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 30649972
[No Abstract] [Full Text] [Related]
3. THREE-DIMENSIONAL CHARACTERISTICS OF FOUR MACULAR INTRARETINAL LAYER THICKNESSES IN SYMPTOMATIC AND ASYMPTOMATIC CARRIERS OF G11778A MUTATION WITH LEBER'S HEREDITARY OPTIC NEUROPATHY.
Huang S; Chen Q; Ma Q; Liu X; Lu F; Shen M
Retina; 2016 Dec; 36(12):2409-2418. PubMed ID: 27870803
[TBL] [Abstract][Full Text] [Related]
4. Retinal nerve fiber layer thickness variability in Leber hereditary optic neuropathy carriers.
Barboni P; Savini G; Feuer WJ; Budenz DL; Carbonelli M; Chicani F; Ramos Cdo V; Salomao SR; Negri AD; Parisi V; Carelli V; Sadun AA
Eur J Ophthalmol; 2012; 22(6):985-91. PubMed ID: 22562299
[TBL] [Abstract][Full Text] [Related]
5. Alterations of the outer retina in non-arteritic anterior ischaemic optic neuropathy detected using spectral-domain optical coherence tomography.
Ackermann P; Brachert M; Albrecht P; Ringelstein M; Finis D; Geerling G; Aktas O; Guthoff R
Clin Exp Ophthalmol; 2017 Jul; 45(5):496-508. PubMed ID: 28133888
[TBL] [Abstract][Full Text] [Related]
6. [Measurement of retinal nerve fiber layer thickness in Leber hereditary optic neuropathy by optical coherence tomography].
Liu Z; Sun CB; Tong Y; Zhang HJ; Zhao GJ; Qu J
Zhonghua Yan Ke Za Zhi; 2012 Oct; 48(10):888-92. PubMed ID: 23302242
[TBL] [Abstract][Full Text] [Related]
7. Retinal nerve fiber layer evaluation by optical coherence tomography in Leber's hereditary optic neuropathy.
Barboni P; Savini G; Valentino ML; Montagna P; Cortelli P; De Negri AM; Sadun F; Bianchi S; Longanesi L; Zanini M; de Vivo A; Carelli V
Ophthalmology; 2005 Jan; 112(1):120-6. PubMed ID: 15629831
[TBL] [Abstract][Full Text] [Related]
8. Retinal Ganglion Cell and Inner Plexiform Layer Loss Correlate with Visual Acuity Loss in LHON: A Longitudinal, Segmentation OCT Analysis.
Moster SJ; Moster ML; Scannell Bryan M; Sergott RC
Invest Ophthalmol Vis Sci; 2016 Jul; 57(8):3872-83. PubMed ID: 27459664
[TBL] [Abstract][Full Text] [Related]
9. 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; 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. PubMed ID: 28196731
[TBL] [Abstract][Full Text] [Related]
10. Foveal pit morphological changes in asymptomatic carriers of the G11778A mutation with Leber's hereditary optic neuropathy.
Liu XT; Shen MX; Chen C; Huang SH; Zhuang XR; Ma QK; Chen Q; Lu F; Yuan YM
Int J Ophthalmol; 2020; 13(5):766-772. PubMed ID: 32420224
[TBL] [Abstract][Full Text] [Related]
11. Retinal nerve fiber layer evaluation by optical coherence tomography in unaffected carriers with Leber's hereditary optic neuropathy mutations.
Savini G; Barboni P; Valentino ML; Montagna P; Cortelli P; De Negri AM; Sadun F; Bianchi S; Longanesi L; Zanini M; Carelli V
Ophthalmology; 2005 Jan; 112(1):127-31. PubMed ID: 15629832
[TBL] [Abstract][Full Text] [Related]
12. Reduction of inner retinal thickness in patients with autosomal dominant optic atrophy associated with OPA1 mutations.
Ito Y; Nakamura M; Yamakoshi T; Lin J; Yatsuya H; Terasaki H
Invest Ophthalmol Vis Sci; 2007 Sep; 48(9):4079-86. PubMed ID: 17724190
[TBL] [Abstract][Full Text] [Related]
13. Ganglion cell loss in relation to visual disability in multiple sclerosis.
Walter SD; Ishikawa H; Galetta KM; Sakai RE; Feller DJ; Henderson SB; Wilson JA; Maguire MG; Galetta SL; Frohman E; Calabresi PA; Schuman JS; Balcer LJ
Ophthalmology; 2012 Jun; 119(6):1250-7. PubMed ID: 22365058
[TBL] [Abstract][Full Text] [Related]
14. Macular thickness changes in a patient with Leber's hereditary optic neuropathy.
Mizoguchi A; Hashimoto Y; Shinmei Y; Nozaki M; Ishijima K; Tagawa Y; Ishida S
BMC Ophthalmol; 2015 Mar; 15():27. PubMed ID: 25885098
[TBL] [Abstract][Full Text] [Related]
15. Macular nerve fibre and ganglion cell layer changes in acute Leber's hereditary optic neuropathy.
Balducci N; Savini G; Cascavilla ML; La Morgia C; Triolo G; Giglio R; Carbonelli M; Parisi V; Sadun AA; Bandello F; Carelli V; Barboni P
Br J Ophthalmol; 2016 Sep; 100(9):1232-7. PubMed ID: 26614631
[TBL] [Abstract][Full Text] [Related]
16. Macular morphology in patients with optic nerve head drusen and optic disc edema.
Pilat AV; Proudlock FA; Kumar P; Lee H; Papageorgiou E; Gottlob I
Ophthalmology; 2014 Feb; 121(2):552-7. PubMed ID: 24238882
[TBL] [Abstract][Full Text] [Related]
17. Thickness mapping of individual retinal layers and sectors by Spectralis SD-OCT in Autosomal Dominant Optic Atrophy.
Corajevic N; Larsen M; Rönnbäck C
Acta Ophthalmol; 2018 May; 96(3):251-256. PubMed ID: 29091347
[TBL] [Abstract][Full Text] [Related]
18. Choroidal thickness and the retinal ganglion cell complex in chronic Leber's hereditary optic neuropathy: a prospective study using swept-source optical coherence tomography.
Darvizeh F; Asanad S; Falavarjani KG; Wu J; Tian JJ; Bandello F; Ross-Cisneros FN; Barboni P; Borrelli E; Sadun AA
Eye (Lond); 2020 Sep; 34(9):1624-1630. PubMed ID: 31804625
[TBL] [Abstract][Full Text] [Related]
19. Assessment of the retinal posterior pole in dominant optic atrophy by spectral-domain optical coherence tomography and microperimetry.
Cesareo M; Ciuffoletti E; Martucci A; Sebastiani J; Sorge RP; Lamantea E; Garavaglia B; Ricci F; Cusumano A; Nucci C; Brancati F
PLoS One; 2017; 12(3):e0174560. PubMed ID: 28358911
[TBL] [Abstract][Full Text] [Related]
20. Leber hereditary optic neuropathy gene therapy clinical trial recruitment: year 1.
Lam BL; Feuer WJ; Abukhalil F; Porciatti V; Hauswirth WW; Guy J
Arch Ophthalmol; 2010 Sep; 128(9):1129-35. PubMed ID: 20837795
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
