207 related articles for article (PubMed ID: 8728098)
21. 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
[TBL] [Abstract][Full Text] [Related]
22. [Correlation between clinical and molecular genetic findings in Leber's optic atrophy].
Leo-Kottler B; Christ-Adler M; Reck B; Wissinger B; Zrenner E
Ophthalmologe; 1995 Feb; 92(1):86-92. PubMed ID: 7719084
[TBL] [Abstract][Full Text] [Related]
23. Characterization of the mitochondrial genome in childhood multiple sclerosis. II. Multiple sclerosis without optic neuritis and LHON-associated genes.
Wilichowski E; Ohlenbusch A; Hanefeld F
Neuropediatrics; 1998 Dec; 29(6):307-12. PubMed ID: 10029350
[TBL] [Abstract][Full Text] [Related]
24. Clinical spectrum of Leber's hereditary optic neuropathy.
Kerrison JB; Newman NJ
Clin Neurosci; 1997; 4(5):295-301. PubMed ID: 9292259
[TBL] [Abstract][Full Text] [Related]
25. Mitochondrial DNA mutations in Cuban optic and peripheral neuropathy.
Johns DR; Neufeld MJ; Hedges TR
J Neuroophthalmol; 1994 Sep; 14(3):135-40. PubMed ID: 7804416
[TBL] [Abstract][Full Text] [Related]
26. Clinical correlation of mitochondrial DNA heteroplasmy and Leber's hereditary optic neuropathy.
Isashiki Y; Nakagawa M
Jpn J Ophthalmol; 1991; 35(3):259-67. PubMed ID: 1770665
[TBL] [Abstract][Full Text] [Related]
27. Cuban epidemic optic neuropathy. Mitochondrial DNA analysis.
Johns DR; Sadun AA
J Neuroophthalmol; 1994 Sep; 14(3):130-4. PubMed ID: 7804415
[TBL] [Abstract][Full Text] [Related]
28. 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
[TBL] [Abstract][Full Text] [Related]
29. Cytochrome c oxidase mutations in Leber hereditary optic neuropathy.
Johns DR; Neufeld MJ
Biochem Biophys Res Commun; 1993 Oct; 196(2):810-5. PubMed ID: 8240356
[TBL] [Abstract][Full Text] [Related]
30. Stargardt's type maculopathy in a patient with 11778 Leber's optic neuropathy.
Yen MY; Wei YH; Liu JH
J Neuroophthalmol; 1996 Jun; 16(2):120-3. PubMed ID: 8797169
[TBL] [Abstract][Full Text] [Related]
31. Leber's hereditary optic neuropathy: implications of the sex ratio for linkage studies in families with the 3460 ND1 mutation.
Black GC; Craig IW; Oostra RJ; Norby S; Rosenberg T; Morten K; Laborde A; Poulton J
Eye (Lond); 1995; 9 ( Pt 4)():513-6. PubMed ID: 7498577
[TBL] [Abstract][Full Text] [Related]
32. A multiple sclerosis-like illness in a man harboring the mtDNA 14484 mutation.
Bhatti MT; Newman NJ
J Neuroophthalmol; 1999 Mar; 19(1):28-33. PubMed ID: 10098545
[TBL] [Abstract][Full Text] [Related]
33. Screening for the two most frequent mutations in Leber's hereditary optic neuropathy by duplex PCR based on allele-specific amplification.
Nørby S
Hum Mutat; 1993; 2(4):309-13. PubMed ID: 8401538
[TBL] [Abstract][Full Text] [Related]
34. Association of the LHON 13,708 and 15,257 mitochondrial DNA mutations with neurodegenerative diseases distinct from LHON.
Rödel G; Laubhan R; Scheuerle A; Skowronek P; Haferkamp O
Eur J Med Res; 1996 Jul; 1(10):491-4. PubMed ID: 9438147
[TBL] [Abstract][Full Text] [Related]
35. [Leber's hereditary optic atrophy. A hereditary disease caused by mitochondrial DNA mutation].
Nørby S; Rosenberg T
Ugeskr Laeger; 1990 Oct; 152(43):3149-52. PubMed ID: 2238193
[TBL] [Abstract][Full Text] [Related]
36. Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis.
Kim JY; Hwang JM; Park SS
Ann Neurol; 2002 May; 51(5):630-4. PubMed ID: 12112111
[TBL] [Abstract][Full Text] [Related]
37. The influence of nuclear background on the biochemical expression of 3460 Leber's hereditary optic neuropathy.
Cock HR; Tabrizi SJ; Cooper JM; Schapira AH
Ann Neurol; 1998 Aug; 44(2):187-93. PubMed ID: 9708540
[TBL] [Abstract][Full Text] [Related]
38. Leber's hereditary optic neuropathy.
Letchavanakul A; Dechphongsaphilas W; Dhamcharee V
J Med Assoc Thai; 1999 Oct; 82(10):1051-5. PubMed ID: 10561972
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Preservation of photic blink reflex in Leber's hereditary optic neuropathy.
Nakamura M; Sekiya Y; Yamamoto M
Invest Ophthalmol Vis Sci; 1996 Dec; 37(13):2736-43. PubMed ID: 8977489
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
