These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
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]
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; 33(8):2561-6. PubMed ID: 1634353 [Abstract] [Full Text] [Related]
13. Mitochondrial DNA analysis of Leber's hereditary optic neuropathy. Hiida Y, Mashima Y, Oguchi Y, Uemura Y, Kudoh J, Sakai K, Shimizu N. Jpn J Ophthalmol; 1991 Jul; 35(1):102-6. PubMed ID: 1895564 [Abstract] [Full Text] [Related]
15. Leber's hereditary optic neuroretinopathy (LHON) associated with mitochondrial DNA point mutation G11778A in two Croatian families. Martin-Kleiner I, Gabrilovac J, Bradvica M, Vidović T, Cerovski B, Fumić K, Boranić M. Coll Antropol; 2006 Mar; 30(1):171-4. PubMed ID: 16617593 [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; 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; 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; 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; 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; 38(4):693-700. PubMed ID: 8728098 [Abstract] [Full Text] [Related] Page: [Next] [New Search]