215 related articles for article (PubMed ID: 36743514)
1. Leber's Hereditary Optic Neuropathy with Mitochondrial DNA Mutation G11778A: A Systematic Literature Review and Meta-Analysis.
Yuan J; Zhao J; Ye C; Pang L; Zhang X; Luk A; Du Y; Fan KY; Zhang X; Li B; Chen C
Biomed Res Int; 2023; 2023():1107866. PubMed ID: 36743514
[TBL] [Abstract][Full Text] [Related]
2. The epidemiology and mutation types of Leber's hereditary optic neuropathy in Thailand.
Sathianvichitr K; Sigkaman B; Chirapapaisan N; Laowanapiban P; Padungkiatsagul T; Apinyawasisuk S; Witthayaweerasak J; Chuenkongkaew W
Ann Med; 2022 Dec; 54(1):1601-1607. PubMed ID: 35723074
[TBL] [Abstract][Full Text] [Related]
3. Leber's hereditary optic neuroretinopathy (LHON) associated with mitochondrial DNA point mutation G11778A in two Croatian families.
Martin-Kleiner I; Gabrilovac J; Bradvica M; Vidović T; Cerovski B; Fumić K; Boranić M
Coll Antropol; 2006 Mar; 30(1):171-4. PubMed ID: 16617593
[TBL] [Abstract][Full Text] [Related]
4. Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation.
Qu J; Zhou X; Zhang J; Zhao F; Sun YH; Tong Y; Wei QP; Cai W; Yang L; West CE; Guan MX
Ophthalmology; 2009 Mar; 116(3):558-564.e3. PubMed ID: 19167085
[TBL] [Abstract][Full Text] [Related]
5. Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation.
Cai W; Fu Q; Zhou X; Qu J; Tong Y; Guan MX
J Genet Genomics; 2008 Nov; 35(11):649-55. PubMed ID: 19022198
[TBL] [Abstract][Full Text] [Related]
6. The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation.
Qu J; Li R; Zhou X; Tong Y; Lu F; Qian Y; Hu Y; Mo JQ; West CE; Guan MX
Invest Ophthalmol Vis Sci; 2006 Feb; 47(2):475-83. PubMed ID: 16431939
[TBL] [Abstract][Full Text] [Related]
7. Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation.
Zhou X; Zhang H; Zhao F; Ji Y; Tong Y; Zhang J; Zhang Y; Yang L; Qian Y; Lu F; Qu J; Guan MX
Mol Genet Metab; 2010 Aug; 100(4):379-84. PubMed ID: 20627642
[TBL] [Abstract][Full Text] [Related]
8. [The analysis of Leber's hereditary optic neuropathy associated with mitochondrial tRNAAla C5601T mutation in seven Han Chinese families].
Zhou HH; Dai XN; Lin B; Mi H; Liu XL; Zhao FX; Zhang JJ; Zhou XT; Sun YH; Wei QP; Qu J; Guan MX
Yi Chuan; 2012 Aug; 34(8):1031-42. PubMed ID: 22917908
[TBL] [Abstract][Full Text] [Related]
9. T14484C and T14502C in the mitochondrial ND6 gene are associated with Leber's hereditary optic neuropathy in a Chinese family.
Zhang S; Wang L; Hao Y; Wang P; Hao P; Yin K; Wang QK; Liu M
Mitochondrion; 2008 Jun; 8(3):205-10. PubMed ID: 18440284
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. [The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].
Mao YJ; Qu J; Guan MX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb; 25(1):45-9. PubMed ID: 18247303
[TBL] [Abstract][Full Text] [Related]
12. Visual Outcomes in Leber Hereditary Optic Neuropathy Patients With the m.11778G>A (MTND4) Mitochondrial DNA Mutation.
Newman NJ; Carelli V; Taiel M; Yu-Wai-Man P
J Neuroophthalmol; 2020 Dec; 40(4):547-557. PubMed ID: 32969847
[TBL] [Abstract][Full Text] [Related]
13. Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy.
Liang M; Jiang P; Li F; Zhang J; Ji Y; He Y; Xu M; Zhu J; Meng X; Zhao F; Tong Y; Liu X; Sun Y; Zhou X; Mo JQ; Qu J; Guan MX
Invest Ophthalmol Vis Sci; 2014 Mar; 55(3):1321-31. PubMed ID: 24398099
[TBL] [Abstract][Full Text] [Related]
14. Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy.
Qian Y; Zhou X; Hu Y; Tong Y; Li R; Lu F; Yang H; Mo JQ; Qu J; Guan MX
Biochem Biophys Res Commun; 2005 Jul; 332(2):614-21. PubMed ID: 15896721
[TBL] [Abstract][Full Text] [Related]
15. Frequency of primary mutations of Leber's hereditary optic neuropathy patients in North Indian population.
Mishra A; Devi S; Saxena R; Gupta N; Kabra M; Chowdhury MR
Indian J Ophthalmol; 2017 Nov; 65(11):1156-1160. PubMed ID: 29133642
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Only male matrilineal relatives with Leber's hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation.
Qu J; Li R; Tong Y; Hu Y; Zhou X; Qian Y; Lu F; Guan MX
Biochem Biophys Res Commun; 2005 Mar; 328(4):1139-45. PubMed ID: 15707996
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial DNA mutations with Leber's hereditary optic neuropathy in Japanese patients with open-angle glaucoma.
Inagaki Y; Mashima Y; Fuse N; Ohtake Y; Fujimaki T; Fukuchi T;
Jpn J Ophthalmol; 2006; 50(2):128-34. PubMed ID: 16604388
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Leber's hereditary optic neuropathy: a multifactorial disease.
Yen MY; Wang AG; Wei YH
Prog Retin Eye Res; 2006 Jul; 25(4):381-96. PubMed ID: 16829155
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
