240 related articles for article (PubMed ID: 11741103)
21. [Diagnostic and differential diagnostic potential of mitochondrial DNA assessment in patients with Leber's hereditary optic neuropathy].
Feng X; Pu W; Gao D
Zhonghua Yan Ke Za Zhi; 2001 May; 37(3):174-7. PubMed ID: 11864415
[TBL] [Abstract][Full Text] [Related]
22. [Study on five point mutations in mitochondrial DNA in patients with Leber's hereditary optic neuropathy].
Du PJ; Zhou JW; Jin XM; Li XW; Wang P
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):675-8. PubMed ID: 16331570
[TBL] [Abstract][Full Text] [Related]
23. [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]
24. Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutations.
Pfeffer G; Burke A; Yu-Wai-Man P; Compston DA; Chinnery PF
Neurology; 2013 Dec; 81(24):2073-81. PubMed ID: 24198293
[TBL] [Abstract][Full Text] [Related]
25. Reduced frequency of known mutations in a cohort of LHON patients from India.
Sundaresan P; Kumar SM; Thompson S; Fingert JH
Ophthalmic Genet; 2010 Dec; 31(4):196-9. PubMed ID: 20809775
[TBL] [Abstract][Full Text] [Related]
26. Leber's hereditary optic neuropathy: the spectrum of mitochondrial DNA mutations in Iranian patients.
Houshmand M; Sharifpanah F; Tabasi A; Sanati MH; Vakilian M; Lavasani SH; Joughehdoust S
Ann N Y Acad Sci; 2004 Apr; 1011():345-9. PubMed ID: 15126312
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Leber's hereditary optic neuropathy (LHON) in an Apulian cohort of subjects.
Bianco A; Bisceglia L; Trerotoli P; Russo L; D'Agruma L; Guerriero S; Petruzzella V
Acta Myol; 2017 Sep; 36(3):163-177. PubMed ID: 29774306
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Increase of mitochondrial DNA in blood cells of patients with Leber's hereditary optic neuropathy with 11778 mutation.
Yen MY; Chen CS; Wang AG; Wei YH
Br J Ophthalmol; 2002 Sep; 86(9):1027-30. PubMed ID: 12185132
[TBL] [Abstract][Full Text] [Related]
31. m.3635G>A mutation as a cause of Leber hereditary optic neuropathy.
Kodroń A; Krawczyński MR; Tońska K; Bartnik E
J Clin Pathol; 2014 Jul; 67(7):639-41. PubMed ID: 24747208
[TBL] [Abstract][Full Text] [Related]
32. A simple oligonucleotide biochip capable of rapidly detecting known mitochondrial DNA mutations in Chinese patients with Leber's hereditary optic neuropathy (LHON).
Du WD; Chen G; Cao HM; Jin QH; Liao RF; He XC; Chen DB; Huang SR; Zhao H; Lv YM; Tang HY; Tang XF; Wang YQ; Sun S; Zhao JL; Zhang XJ
Dis Markers; 2011; 30(4):181-90. PubMed ID: 21694444
[TBL] [Abstract][Full Text] [Related]
33. Genotypic and phenotypic characteristics of Korean children with childhood-onset Leber's hereditary optic neuropathy.
Ahn YJ; Park Y; Shin SY; Chae H; Kim M; Park SH
Graefes Arch Clin Exp Ophthalmol; 2020 Oct; 258(10):2283-2290. PubMed ID: 32506279
[TBL] [Abstract][Full Text] [Related]
34. [Rapid genetic screening of Leber's hereditary optic neuropathy with mtDNA G11778A mutation by AS-PCR with whole blood].
Yang JH; Tong Y; Li BH; Chen YK
Zhonghua Yan Ke Za Zhi; 2005 Mar; 41(3):243-5. PubMed ID: 15840367
[TBL] [Abstract][Full Text] [Related]
35. A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy.
Mimaki M; Ikota A; Sato A; Komaki H; Akanuma J; Nonaka I; Goto Y
J Hum Genet; 2003; 48(1):47-50. PubMed ID: 12560876
[TBL] [Abstract][Full Text] [Related]
36. Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations.
Fauser S; Luberichs J; Besch D; Leo-Kottler B
Biochem Biophys Res Commun; 2002 Jul; 295(2):342-7. PubMed ID: 12150954
[TBL] [Abstract][Full Text] [Related]
37. Clinical analysis of Leber's hereditary optic neuropathy harboring mtDNA mutation at nt11778.
Zhang X; Yu Q; Zhang Q; Yi C
Yan Ke Xue Bao; 2001 Mar; 17(1):31-4. PubMed ID: 12567592
[TBL] [Abstract][Full Text] [Related]
38. Phylogenetic assessment of the mitochondrial DNA displacement loop haplotype in Japanese patients with Leber's hereditary optic neuropathy harboring the mitochondrial DNA G11778A mutation.
Isashiki Y; Sonoda S; Izumo S; Sakamoto T; Tachikui H; Inoue I
Ophthalmic Res; 2003; 35(4):224-31. PubMed ID: 12815198
[TBL] [Abstract][Full Text] [Related]
39. No association of the 11778 mitochondrial DNA mutation and multiple sclerosis in Japan.
Nishimura M; Obayashi H; Ohta M; Uchiyama T; Hao Q; Saida T
Neurology; 1995 Jul; 45(7):1333-4. PubMed ID: 7617193
[TBL] [Abstract][Full Text] [Related]
40. Whole Mitochondrial Genome Analysis in Serbian Cases of Leber's Hereditary Optic Neuropathy.
Dawod PGA; Jancic J; Marjanovic A; Brankovic M; Jankovic M; Samardzic J; Potkonjak D; Djuric V; Mesaros S; Novakovic I; Abdel Motaleb FI; Kostic VS; Nikolic D
Genes (Basel); 2020 Sep; 11(9):. PubMed ID: 32887465
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]