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Journal Abstract Search
163 related items for PubMed ID: 8404350
1. [A molecular genetic study of Leber's disease]. Zhang LS. Zhonghua Yan Ke Za Zhi; 1993 Mar; 29(2):103-4. PubMed ID: 8404350 [Abstract] [Full Text] [Related]
2. [Mitochondrial DNA mutation in Leber's hereditary optic neuropathy in China]. Zhang LS, Huang Y, Li FY. Zhonghua Yi Xue Za Zhi; 1994 Jun; 74(6):349-51, 390. PubMed ID: 7994643 [Abstract] [Full Text] [Related]
3. 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]
4. Quantitative determination of heteroplasmy in Leber's hereditary optic neuropathy by single-strand conformation polymorphism. Mashima Y, Saga M, Hiida Y, Oguchi Y, Wakakura M, Kudoh J, Shimizu N. Invest Ophthalmol Vis Sci; 1995 Jul; 36(8):1714-20. PubMed ID: 7601652 [Abstract] [Full Text] [Related]
8. 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]
10. 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]
11. Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene. Leo-Kottler B, Christ-Adler M, Baumann B, Zrenner E, Wissinger B. Ger J Ophthalmol; 1996 Jul; 5(4):233-40. PubMed ID: 8854108 [Abstract] [Full Text] [Related]
12. [Leber's hereditary optic atrophy. A hereditary disease caused by mitochondrial DNA mutation]. Nørby S, Rosenberg T. Ugeskr Laeger; 1990 Oct 22; 152(43):3149-52. PubMed ID: 2238193 [Abstract] [Full Text] [Related]
13. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations]. Pénisson-Besnier I, Moreau C, Jacques C, Roger JC, Dubas F, Reynier P. Rev Neurol (Paris); 2001 May 22; 157(5):537-41. PubMed ID: 11438773 [Abstract] [Full Text] [Related]