238 related articles for article (PubMed ID: 8600429)
41. Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism.
Vilkki J; Savontaus ML; Nikoskelainen EK
Am J Hum Genet; 1989 Aug; 45(2):206-11. PubMed ID: 2757028
[TBL] [Abstract][Full Text] [Related]
42. 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
[TBL] [Abstract][Full Text] [Related]
43. [Analysis on the effect of secondary mutations on Leber's hereditary optic neuropathy].
Wang Y; Tong Y; Hu SX; Wang JY; Shao JB; Zhang HX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):397-400. PubMed ID: 17680528
[TBL] [Abstract][Full Text] [Related]
44. 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]
45. Intrafamilial variation in Leber hereditary optic neuropathy revealed by direct mutation analysis.
Cavelier L; Gyllensten U; Dahl N
Clin Genet; 1993 Feb; 43(2):69-72. PubMed ID: 8448903
[TBL] [Abstract][Full Text] [Related]
46. The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees.
Phasukkijwatana N; Chuenkongkaew WL; Suphavilai R; Suktitipat B; Pingsuthiwong S; Ruangvaravate N; Atchaneeyasakul LO; Warrasak S; Poonyathalang A; Sura T; Lertrit P
J Hum Genet; 2006; 51(4):298-304. PubMed ID: 16477364
[TBL] [Abstract][Full Text] [Related]
47. Optic neuropathy in Lhon and Leigh syndrome.
Carelli V; Sadun AA
Ophthalmology; 2001 Jul; 108(7):1172-3. PubMed ID: 11425664
[No Abstract] [Full Text] [Related]
48. The epidemiology of Leber hereditary optic neuropathy in the North East of England.
Yu-Wai-Man P; Griffiths PG; Brown DT; Howell N; Turnbull DM; Chinnery PF
Am J Hum Genet; 2003 Feb; 72(2):333-9. PubMed ID: 12518276
[TBL] [Abstract][Full Text] [Related]
49. Pedigree analysis of French Canadian families with T14484C Leber's hereditary optic neuropathy.
Macmillan C; Kirkham T; Fu K; Allison V; Andermann E; Chitayat D; Fortier D; Gans M; Hare H; Quercia N; Zackon D; Shoubridge EA
Neurology; 1998 Feb; 50(2):417-22. PubMed ID: 9484365
[TBL] [Abstract][Full Text] [Related]
50. [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; 157(5):537-41. PubMed ID: 11438773
[TBL] [Abstract][Full Text] [Related]
51. [Leber's optic nerve atrophy; a mitochondrial hereditary disease].
Oostra RJ; Bolhuis PA; Wijburg FA; Bleeker-Wagemakers EM
Ned Tijdschr Geneeskd; 1995 Jul; 139(26):1327-31. PubMed ID: 7617050
[TBL] [Abstract][Full Text] [Related]
52. The spectrum of mitochondrial DNA mutations in families with Leber hereditary optic neuroretinopathy.
Huoponen K; Lamminen T; Juvonen V; Aula P; Nikoskelainen E; Savontaus ML
Hum Genet; 1993 Oct; 92(4):379-84. PubMed ID: 7901141
[TBL] [Abstract][Full Text] [Related]
53. Visual recovery in a patient with Leber hereditary optic neuropathy and the 14484 mutation.
Hrynchak PK; Spafford MM
Optom Vis Sci; 1994 Oct; 71(10):604-12. PubMed ID: 7877803
[TBL] [Abstract][Full Text] [Related]
54. Leber's hereditary optic neuropathy mitochondrial DNA mutations at nucleotides 11778 and 3460 in multiple sclerosis.
Mojon DS; Herbert J; Sadiq SA; Miller JR; Madonna M; Hirano M
Ophthalmologica; 1999; 213(3):171-5. PubMed ID: 10202290
[TBL] [Abstract][Full Text] [Related]
55. 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]
56. [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]
57. Leber's hereditary optic neuropathy. Clinical manifestations of the 3460 mutation.
Johns DR; Smith KH; Miller NR
Arch Ophthalmol; 1992 Nov; 110(11):1577-81. PubMed ID: 1444915
[TBL] [Abstract][Full Text] [Related]
58. mtDNA haplotype analysis in Finnish families with leber hereditary optic neuroretinopathy.
Lamminen T; Huoponen K; Sistonen P; Juvonen V; Lahermo P; Aula P; Nikoskelainen E; Savontaus ML
Eur J Hum Genet; 1997; 5(5):271-9. PubMed ID: 9412783
[TBL] [Abstract][Full Text] [Related]
59. [Penetrance of Leber hereditary optic neuropathy in Chinese individuals with mitochondrial DNA 11778 mutation].
Zhang Q; Guo X; Jia X; Xiao X; Guo L; Li S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Dec; 18(6):441-3. PubMed ID: 11774211
[TBL] [Abstract][Full Text] [Related]
60. 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]
[Previous] [Next] [New Search]
