192 related articles for article (PubMed ID: 7635294)
1. Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees.
Howell N; Kubacka I; Halvorson S; Howell B; McCullough DA; Mackey D
Genetics; 1995 May; 140(1):285-302. PubMed ID: 7635294
[TBL] [Abstract][Full Text] [Related]
2. Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy.
Howell N; Oostra RJ; Bolhuis PA; Spruijt L; Clarke LA; Mackey DA; Preston G; Herrnstadt C
Am J Hum Genet; 2003 Jun; 72(6):1460-9. PubMed ID: 12736867
[TBL] [Abstract][Full Text] [Related]
3. The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.
Chinnery PF; Brown DT; Andrews RM; Singh-Kler R; Riordan-Eva P; Lindley J; Applegarth DA; Turnbull DM; Howell N
Brain; 2001 Jan; 124(Pt 1):209-18. PubMed ID: 11133798
[TBL] [Abstract][Full Text] [Related]
4. A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology.
Mackey D; Howell N
Am J Hum Genet; 1992 Dec; 51(6):1218-28. PubMed ID: 1463007
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.
Brown MD; Sun F; Wallace DC
Am J Hum Genet; 1997 Feb; 60(2):381-7. PubMed ID: 9012411
[TBL] [Abstract][Full Text] [Related]
7. Leber hereditary optic neuropathy: mitochondrial mutations and degeneration of the optic nerve.
Howell N
Vision Res; 1997 Dec; 37(24):3495-507. PubMed ID: 9425526
[TBL] [Abstract][Full Text] [Related]
8. Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population.
Dogulu CF; Kansu T; Seyrantepe V; Ozguc M; Topaloglu H; Johns DR
Eye (Lond); 2001 Apr; 15(Pt 2):183-8. PubMed ID: 11339587
[TBL] [Abstract][Full Text] [Related]
9. Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations.
Brown MD; Torroni A; Reckord CL; Wallace DC
Hum Mutat; 1995; 6(4):311-25. PubMed ID: 8680405
[TBL] [Abstract][Full Text] [Related]
10. High frequency of mitochondrial ND4 gene mutation in Japanese pedigrees with Leber hereditary optic neuropathy.
Nakamura M; Ara F; Yamada M; Hotta Y; Hayakawa M; Fujiki K; Kanai A; Sakai J; Inoue M; Yamamoto M
Jpn J Ophthalmol; 1992; 36(1):56-61. PubMed ID: 1635296
[TBL] [Abstract][Full Text] [Related]
11. Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis.
Vanopdenbosch L; Dubois B; D'Hooghe MB; Meire F; Carton H
J Neurol; 2000 Jul; 247(7):535-43. PubMed ID: 10993496
[TBL] [Abstract][Full Text] [Related]
12. Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutations.
Nikoskelainen EK; Huoponen K; Juvonen V; Lamminen T; Nummelin K; Savontaus ML
Ophthalmology; 1996 Mar; 103(3):504-14. PubMed ID: 8600429
[TBL] [Abstract][Full Text] [Related]
13. 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
[TBL] [Abstract][Full Text] [Related]
14. Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathy.
Matsumoto M; Hayasaka S; Kadoi C; Hotta Y; Fujiki K; Fujimaki T; Takeda M; Ishida N; Endo S; Kanai A
Ophthalmic Genet; 1999 Sep; 20(3):153-60. PubMed ID: 10520236
[TBL] [Abstract][Full Text] [Related]
15. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes.
Hofmann S; Bezold R; Jaksch M; Obermaier-Kusser B; Mertens S; Kaufhold P; Rabl W; Hecker W; Gerbitz KD
Genomics; 1997 Jan; 39(1):8-18. PubMed ID: 9027481
[TBL] [Abstract][Full Text] [Related]
16. Sporadic Leber hereditary optic neuropathy in Australia and New Zealand.
Chan C; Mackey DA; Byrne E
Aust N Z J Ophthalmol; 1996 Feb; 24(1):7-14. PubMed ID: 8742999
[TBL] [Abstract][Full Text] [Related]
17. LHON mutations in Italian patients affected by multiple sclerosis.
Leuzzi V; Carducci C; Lenza M; Salvetti M; Ristori G; Di Giovanni S; Torroni A
Acta Neurol Scand; 1997 Sep; 96(3):145-8. PubMed ID: 9300066
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. mtDNA analysis of Leber hereditary optic neuropathy associated with spondyloepiphyseal dysplasia.
Howell N; Kubacka I; McDonough B; Hodess AB; Harter DH
Am J Med Genet; 2001 May; 100(3):219-22. PubMed ID: 11343307
[TBL] [Abstract][Full Text] [Related]
20. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
PĂ©nisson-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]
[Next] [New Search]