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Journal Abstract Search
445 related items for PubMed ID: 19247386
1. 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; 24(1):107-11. PubMed ID: 19247386 [Abstract] [Full Text] [Related]
2. 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 [Abstract] [Full Text] [Related]
3. Leber's hereditary optic neuropathy with childhood onset. Barboni P, Savini G, Valentino ML, La Morgia C, Bellusci C, De Negri AM, Sadun F, Carta A, Carbonelli M, Sadun AA, Carelli V. Invest Ophthalmol Vis Sci; 2006 Dec; 47(12):5303-9. PubMed ID: 17122117 [Abstract] [Full Text] [Related]
10. Retinal ganglion cell analysis in Leber's hereditary optic neuropathy. Akiyama H, Kashima T, Li D, Shimoda Y, Mukai R, Kishi S. Ophthalmology; 2013 Sep; 120(9):1943-4.e5. PubMed ID: 24001531 [No Abstract] [Full Text] [Related]
11. [A pedigree of Leber's hereditary optic neuropathy with mtDNA 14484 mutation]. Tong Y, Wang Y, Jiang F, Liu B, Zhang S, Yang W. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):531-3. PubMed ID: 18841565 [Abstract] [Full Text] [Related]
14. 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]
16. Myelinated retinal nerve fibres loss in Leber's hereditary optic neuropathy. Gicquel JJ, Salama B, Mercié M, Bonneau D, Dighiero P. Acta Ophthalmol Scand; 2005 Aug 03; 83(4):517-8. PubMed ID: 16029287 [No Abstract] [Full Text] [Related]
17. White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation. Lev D, Yanoov-Sharav M, Watemberg N, Leshinsky-Silver E, Lerman-Sagie T. Eur J Paediatr Neurol; 2002 Aug 03; 6(2):121-3. PubMed ID: 11995959 [Abstract] [Full Text] [Related]