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265 related items for PubMed ID: 32862131
1. Characterisation of thickness changes in the peripapillary retinal nerve fibre layer in patients with Leber's hereditary optic neuropathy. Wang D, Liu HL, Du YY, Yuan J, Li X, Tian Z, Zhou H, Wang S, Song L, Sun J, Xiao X, Wang ZT, Li B. Br J Ophthalmol; 2021 Aug; 105(8):1166-1171. PubMed ID: 32862131 [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 [Abstract] [Full Text] [Related]
3. 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 [Abstract] [Full Text] [Related]
8. Clinical follow-up investigation on thickness changes in the peripapillary retinal nerve fibre layer of patients with Leber hereditary optic neuropathy. Wang D, Yuan J, Liu HL, Li SL, Ma N, Chen ML, Yuan H, Jie H, Li B, Zhang T. BMC Ophthalmol; 2024 Aug 15; 24(1):348. PubMed ID: 39148060 [Abstract] [Full Text] [Related]
9. 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 15; 112(1):127-31. PubMed ID: 15629832 [Abstract] [Full Text] [Related]
10. Characterization of macular thickness changes in Leber's hereditary optic neuropathy by optical coherence tomography. Zhang Y, Huang H, Wei S, Gong Y, Li H, Dai Y, Zhao S, Wang Y, Yan H. BMC Ophthalmol; 2014 Sep 01; 14():105. PubMed ID: 25179213 [Abstract] [Full Text] [Related]
11. PhNR and peripapillary RNFL changes in Leber hereditary optic neuropathy with m.G11778A mutation. Miao Q, Cheng Y, Zheng H, Yuan J, Chen C. Mitochondrion; 2023 May 01; 70():111-117. PubMed ID: 37127073 [Abstract] [Full Text] [Related]
12. 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 18; 15():27. PubMed ID: 25885098 [Abstract] [Full Text] [Related]
13. Longitudinal Study of Optic Disk Perfusion and Retinal Structure in Leber's Hereditary Optic Neuropathy. Calzetti G, La Morgia C, Cattaneo M, Carta A, Bosello F, Amore G, Carbonelli M, Cascavilla ML, Gandolfi S, Carelli V, Schmetterer L, Scholl HPN, Barboni P. Invest Ophthalmol Vis Sci; 2022 Jan 03; 63(1):43. PubMed ID: 35098304 [Abstract] [Full Text] [Related]
14. Comparison of retinal nerve fibre layers between 11778 and 14484 mutations in Leber's hereditary optic neuropathy. Seo JH, Hwang JM, Park SS. Eye (Lond); 2010 Jan 03; 24(1):107-11. PubMed ID: 19247386 [Abstract] [Full Text] [Related]
16. 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 01; 47(9):802-10. PubMed ID: 27631475 [Abstract] [Full Text] [Related]
17. OCT in Alzheimer's disease: thinning of the RNFL and superior hemiretina. Cunha JP, Proença R, Dias-Santos A, Almeida R, Águas H, Alves M, Papoila AL, Louro C, Castanheira-Dinis A. Graefes Arch Clin Exp Ophthalmol; 2017 Sep 01; 255(9):1827-1835. PubMed ID: 28643042 [Abstract] [Full Text] [Related]
18. 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 01; 100(9):1232-7. PubMed ID: 26614631 [Abstract] [Full Text] [Related]
19. Leber hereditary optic neuropathy due to a new ND1 mutation. Soldath P, Wegener M, Sander B, Rosenberg T, Duno M, Wibrand F, Vissing J. Ophthalmic Genet; 2017 Sep 01; 38(5):480-485. PubMed ID: 28139165 [Abstract] [Full Text] [Related]
20. Peripapillary vessel density changes in Leber's hereditary optic neuropathy: a new biomarker. Balducci N, Cascavilla ML, Ciardella A, La Morgia C, Triolo G, Parisi V, Bandello F, Sadun AA, Carelli V, Barboni P. Clin Exp Ophthalmol; 2018 Dec 01; 46(9):1055-1062. PubMed ID: 29790285 [Abstract] [Full Text] [Related] Page: [Next] [New Search]