291 related articles for article (PubMed ID: 10202290)
1. 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]
2. Leber's hereditary optic neuropathy mitochondrial DNA mutations in familial multiple sclerosis.
Mojon DS; Fujihara K; Hirano M; Miller C; Lincoff NS; Jacobs LD; Greenberg SJ
Graefes Arch Clin Exp Ophthalmol; 1999 Apr; 237(4):348-50. PubMed ID: 10208269
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. 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]
5. 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]
6. Leber's hereditary optic neuropathy mutations in Korean patients with multiple sclerosis.
Hwang JM; Chang BL; Park SS
Ophthalmologica; 2001; 215(6):398-400. PubMed ID: 11741103
[TBL] [Abstract][Full Text] [Related]
7. Leber's hereditary optic neuropathy (LHON)-related mitochondrial DNA sequence changes in italian patients presenting with sporadic bilateral optic neuritis.
Sartore M; Grasso M; Piccolo G; Fasani R; Bergamaschi R; Malaspina A; Ceroni M; Kobayashi M; Semeraro A; Arbustini E
Biochem Mol Med; 1995 Oct; 56(1):45-51. PubMed ID: 8593537
[TBL] [Abstract][Full Text] [Related]
8. Lack of association between Leber's hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran.
Houshmand M; Sanati MH; Rashedi I; Sharifpanah F; Asghari E; Lotfi J
Eur Neurol; 2004; 51(2):68-71. PubMed ID: 14671420
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHON.
Gerbitz KD; Paprotta A; Obermaier-Kusser B; Rietschel M; Zerres K
FEBS Lett; 1992 Dec; 314(3):251-5. PubMed ID: 1361456
[TBL] [Abstract][Full Text] [Related]
11. Screening for Leber's hereditary optic neuropathy associated mitochondrial DNA mutations in patients with prominent optic neuritis.
Kalman B; Rodriguez-Valdez JL; Bosch U; Lublin FD
Mult Scler; 1997 Jan; 2(6):279-82. PubMed ID: 9065918
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. No evidence of association between optic neuritis and secondary LHON mtDNA mutations in patients with multiple sclerosis.
Andalib S; Talebi M; Sakhinia E; Farhoudi M; Sadeghi-Bazargani H; Masoudian N; Vafaee MS; Gjedde A
Mitochondrion; 2017 Sep; 36():182-185. PubMed ID: 28802665
[TBL] [Abstract][Full Text] [Related]
14. Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy.
Jacobi FK; Leo-Kottler B; Mittelviefhaus K; Zrenner E; Meyer J; Pusch CM; Wissinger B
Invest Ophthalmol Vis Sci; 2001 May; 42(6):1208-14. PubMed ID: 11328729
[TBL] [Abstract][Full Text] [Related]
15. Leber's hereditary optic neuropathy mitochondrial DNA mutations in normal-tension glaucoma.
Opial D; Boehnke M; Tadesse S; Lietz-Partzsch A; Flammer J; Munier F; Mermoud A; Hirano M; Flückiger F; Mojon DS
Graefes Arch Clin Exp Ophthalmol; 2001 Jul; 239(6):437-40. PubMed ID: 11561792
[TBL] [Abstract][Full Text] [Related]
16. Nonfamilial and unusual cases of Leber's hereditary optic neuropathy identified by mitochondrial DNA analysis.
Isashiki Y; Ohba N; Uto M; Nakagawa M; Nakano T; Kitahara K; Hotta A; Okamura R; Ozaki M; Futami Y
Jpn J Ophthalmol; 1992; 36(2):197-204. PubMed ID: 1513067
[TBL] [Abstract][Full Text] [Related]
17. 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
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. 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]
20. 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]
[Next] [New Search]
