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981 related items for PubMed ID: 30649972
1. 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]
2. 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]
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]
4. 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]
18. 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]
19. Changes in Choroidal Thickness follow the RNFL Changes in Leber's Hereditary Optic Neuropathy. Borrelli E, Triolo G, Cascavilla ML, La Morgia C, Rizzo G, Savini G, Balducci N, Nucci P, Giglio R, Darvizeh F, Parisi V, Bandello F, Sadun AA, Carelli V, Barboni P. Sci Rep; 2016 Nov 17; 6():37332. PubMed ID: 27853297 [Abstract] [Full Text] [Related]
20. Variation in retinal nerve fiber layer thickness at different stages of Leber's hereditary optic neuropathy in patients with the ND4 G11778A mutation. Tian Z, Li X, Zheng W, Li B, Zhang Y. Semin Ophthalmol; 2022 May 19; 37(4):496-501. PubMed ID: 34702118 [Abstract] [Full Text] [Related] Page: [Next] [New Search]