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4. High incidence of visual recovery among four Japanese patients with Leber's hereditary optic neuropathy with the 14484 mutation. Yamada K, Mashima Y, Kigasawa K, Miyashita K, Wakakura M, Oguchi Y. J Neuroophthalmol; 1997 Jun; 17(2):103-7. PubMed ID: 9176781 [Abstract] [Full Text] [Related]
5. Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA. Hotta Y, Fujiki K, Hayakawa M, Nakajima A, Kanai A, Mashima Y, Hiida Y, Shinoda K, Yamada K, Oguchi Y. Jpn J Ophthalmol; 1995 Jun; 39(1):96-108. PubMed ID: 7643491 [Abstract] [Full Text] [Related]
12. Mitochondrial DNA mutation in Leber's hereditary optic neuropathy. Yen MY, Yen TC, Pang CY, Liu JH, Wei YH. Invest Ophthalmol Vis Sci; 1992 Jul 20; 33(8):2561-6. PubMed ID: 1634353 [Abstract] [Full Text] [Related]
14. Preservation of photic blink reflex in Leber's hereditary optic neuropathy. Nakamura M, Sekiya Y, Yamamoto M. Invest Ophthalmol Vis Sci; 1996 Dec 20; 37(13):2736-43. PubMed ID: 8977489 [Abstract] [Full Text] [Related]
16. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis. Kellar-Wood H, Robertson N, Govan GG, Compston DA, Harding AE. Ann Neurol; 1994 Jul 20; 36(1):109-12. PubMed ID: 8024249 [Abstract] [Full Text] [Related]
17. Leber's hereditary optic neuropathy: clinical and molecular genetic results in a patient with a point mutation at np T11253C (isoleucine to threonine) in the ND4 gene and spontaneous recovery. Leo-Kottler B, Luberichs J, Besch D, Christ-Adler M, Fauser S. Graefes Arch Clin Exp Ophthalmol; 2002 Sep 20; 240(9):758-64. PubMed ID: 12271374 [Abstract] [Full Text] [Related]
18. Genetic analysis of Japanese pedigrees with Leber's hereditary optic neuropathy. Nakamura M. Kobe J Med Sci; 1993 Dec 20; 39(5-6):171-82. PubMed ID: 8182918 [Abstract] [Full Text] [Related]
19. [Diagnostic and differential diagnostic potential of mitochondrial DNA assessment in patients with Leber's hereditary optic neuropathy]. Feng X, Pu W, Gao D. Zhonghua Yan Ke Za Zhi; 2001 May 20; 37(3):174-7. PubMed ID: 11864415 [Abstract] [Full Text] [Related]
20. Mitochondrial DNA mutations associated with the 11778 mutation in Leber's disease. Sawano T, Tanaka M, Ohno K, Yoneda M, Ota Y, Terasaki H, Awaya S, Ozawa T. Biochem Mol Biol Int; 1996 Apr 20; 38(4):693-700. PubMed ID: 8728098 [Abstract] [Full Text] [Related] Page: [Next] [New Search]