124 related articles for article (PubMed ID: 8115116)
1. Leber's hereditary optic neuropathy. Is it a disease of northern Europe and Asia?
Mackey DA
Ophthalmic Paediatr Genet; 1993 Sep; 14(3):105-7. PubMed ID: 8115116
[No Abstract] [Full Text] [Related]
2. 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
[TBL] [Abstract][Full Text] [Related]
3. Leber's hereditary optic neuropathy among Japanese.
Ishikawa S; Ichibe Y; Yokoe J; Wakakura M
Muscle Nerve Suppl; 1995; 3():S85-9. PubMed ID: 7603534
[TBL] [Abstract][Full Text] [Related]
4. Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathy.
Yoneda M; Tsuji S; Yamauchi T; Inuzuka T; Miyatake T; Horai S; Ozawa T
Lancet; 1989 May; 1(8646):1076-7. PubMed ID: 2566021
[No Abstract] [Full Text] [Related]
5. Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation.
Shoffner JM; Brown MD; Stugard C; Jun AS; Pollock S; Haas RH; Kaufman A; Koontz D; Kim Y; Graham JR
Ann Neurol; 1995 Aug; 38(2):163-9. PubMed ID: 7654063
[TBL] [Abstract][Full Text] [Related]
6. [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
[TBL] [Abstract][Full Text] [Related]
7. Mitochondrial DNA mutations in Leber's optic neuropathy.
Hurko O
Ann Neurol; 1994 May; 35(5):636. PubMed ID: 7910006
[No Abstract] [Full Text] [Related]
8. The molecular genetics of Leber's hereditary optic neuropathy.
Johns DR
Arch Ophthalmol; 1990 Oct; 108(10):1405-7. PubMed ID: 2222273
[No Abstract] [Full Text] [Related]
9. Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy.
Johns DR; Berman J
Biochem Biophys Res Commun; 1991 Feb; 174(3):1324-30. PubMed ID: 1900003
[TBL] [Abstract][Full Text] [Related]
10. De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathy.
Biousse V; Brown MD; Newman NJ; Allen JC; Rosenfeld J; Meola G; Wallace DC
Neurology; 1997 Oct; 49(4):1136-8. PubMed ID: 9339703
[TBL] [Abstract][Full Text] [Related]
11. Leber's hereditary optic neuropathy.
Volpe NJ; Lessell S
Int Ophthalmol Clin; 1993; 33(2):153-68. PubMed ID: 8325730
[No Abstract] [Full Text] [Related]
12. Mitochondria and Leber's hereditary optic neuropathy.
Newman NJ; Wallace DC
Am J Ophthalmol; 1990 Jun; 109(6):726-30. PubMed ID: 2346203
[No Abstract] [Full Text] [Related]
13. The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.
Newman NJ; Lott MT; Wallace DC
Am J Ophthalmol; 1991 Jun; 111(6):750-62. PubMed ID: 2039048
[TBL] [Abstract][Full Text] [Related]
14. Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation.
Harding AE; Sweeney MG; Miller DH; Mumford CJ; Kellar-Wood H; Menard D; McDonald WI; Compston DA
Brain; 1992 Aug; 115 ( Pt 4)():979-89. PubMed ID: 1393514
[TBL] [Abstract][Full Text] [Related]
15. Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy.
Holt IJ; Miller DH; Harding AE
J Neurol Neurosurg Psychiatry; 1988 Aug; 51(8):1075-7. PubMed ID: 2905730
[TBL] [Abstract][Full Text] [Related]
16. Leber's hereditary optic neuropathy. Clinical manifestations of the 15257 mutation.
Johns DR; Smith KH; Savino PJ; Miller NR
Ophthalmology; 1993 Jul; 100(7):981-6. PubMed ID: 8321540
[TBL] [Abstract][Full Text] [Related]
17. Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy.
Poulton J; Deadman ME; Bronte-Stewart J; Foulds WS; Gardiner RM
J Med Genet; 1991 Nov; 28(11):765-70. PubMed ID: 1770533
[TBL] [Abstract][Full Text] [Related]
18. Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation.
Murakami T; Mita S; Tokunaga M; Maeda H; Ueyama H; Kumamoto T; Uchino M; Ando M
J Neurol Sci; 1996 Oct; 142(1-2):111-3. PubMed ID: 8902729
[TBL] [Abstract][Full Text] [Related]
19. Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy.
Bolhuis PA; Bleeker-Wagemakers EM; Ponne NJ; Van Schooneveld MJ; Westerveld A; Van den Bogert C; Tabak HF
Biochem Biophys Res Commun; 1990 Aug; 170(3):994-7. PubMed ID: 2390098
[TBL] [Abstract][Full Text] [Related]
20. A new mitochondrial DNA mutation in the tRNA leucine 1 gene (C3275A) in a patient with Leber's hereditary optic neuropathy.
Garcia-Lozano JR; Aguilera I; Bautista J; Nuñez-Roldan A
Hum Mutat; 2000 Jan; 15(1):120-1. PubMed ID: 10612844
[No Abstract] [Full Text] [Related]
[Next] [New Search]
