193 related articles for article (PubMed ID: 23091534)
21. Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation.
Murakami T; Mita S; Tokunaga M; Maeda H; Ueyama H; Kumamoto T; Uchino M; Ando M
J Neurol Sci; 1996 Oct; 142(1-2):111-3. PubMed ID: 8902729
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Aberrant neurovascular coupling in Leber's hereditary optic neuropathy: Evidence from a multi-model MRI analysis.
Ji Y; Wang L; Ding H; Tian Q; Fan K; Shi D; Yu C; Qin W
Front Neurosci; 2022; 16():1050772. PubMed ID: 36703998
[TBL] [Abstract][Full Text] [Related]
24. Optical Coherence Tomography of the Retinal Ganglion Cell Complex in Leber's Hereditary Optic Neuropathy and Dominant Optic Atrophy.
Asanad S; Tian JJ; Frousiakis S; Jiang JP; Kogachi K; Felix CM; Fatemeh D; Irvine AG; Ter-Zakarian A; Falavarjani KG; Barboni P; Karanjia R; Sadun AA
Curr Eye Res; 2019 Jun; 44(6):638-644. PubMed ID: 30649972
[No Abstract] [Full Text] [Related]
25. A Female Patient with Down Syndrome and Low-Penetrance Leber's Hereditary Optic Neuropathy.
Frousiakis SE; Pouw AE; Karanjia R; Sadun AA
Case Rep Ophthalmol; 2014 Sep; 5(3):405-10. PubMed ID: 25566062
[TBL] [Abstract][Full Text] [Related]
26. Cerebellar ataxia in patients with Leber's hereditary optic neuropathy.
Funakawa I; Kato H; Terao A; Ichihashi K; Kawashima S; Hayashi T; Mitani K; Miyazaki S
J Neurol; 1995 Jan; 242(2):75-7. PubMed ID: 7707093
[TBL] [Abstract][Full Text] [Related]
27. Compressive Optic Neuropathy with a Concurrent Mutation of Leber's Hereditary Optic Neuropathy: A Case Report.
Park Y; Ohn K; Ahn YJ; Jang J; Park SH
Neuroophthalmology; 2020; 44(6):387-390. PubMed ID: 33335345
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. [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]
30. Leber's hereditary optic neuropathy following unilateral painful optic neuritis: a case report.
Lee C; Park KA; Lee GI; Oh SY; Min JH; Kim BJ
BMC Ophthalmol; 2020 May; 20(1):195. PubMed ID: 32423393
[TBL] [Abstract][Full Text] [Related]
31. Clinically Diagnosed Occult Macular Dystrophy Habouring an m.14502T>C Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy: Case Report and Literature Review.
Zhou HP; Sawamura H; Nakamura N; Yamagami A; Yasumoto R; Kasai K; Obata R; Aihara M
Neuroophthalmology; 2023; 47(5-6):285-290. PubMed ID: 38130805
[TBL] [Abstract][Full Text] [Related]
32. [Rapid onset of visual recovery following acute visual loss due to leber's hereditary optic neuropathy].
Kawasaki A; Borruat FX
Rev Neurol (Paris); 2005 May; 161(5):599-601. PubMed ID: 16106816
[TBL] [Abstract][Full Text] [Related]
33. Impaired mitochondrial morphological plasticity and failure of mitophagy associated with the G11778A mutation of LHON.
Pasqualotto BA; Nelson A; Deheshi S; Sheldon CA; Vogl AW; Rintoul GL
Biochem Biophys Res Commun; 2024 Aug; 721():150119. PubMed ID: 38768545
[TBL] [Abstract][Full Text] [Related]
34. Characterization of a Leber's hereditary optic neuropathy (LHON) family harboring two primary LHON mutations m.11778G>A and m.14484T>C of the mitochondrial DNA.
Catarino CB; Ahting U; Gusic M; Iuso A; Repp B; Peters K; Biskup S; von Livonius B; Prokisch H; Klopstock T
Mitochondrion; 2017 Sep; 36():15-20. PubMed ID: 27721048
[TBL] [Abstract][Full Text] [Related]
35. [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]
36. Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.
Sudoyo H; Suryadi H; Lertrit P; Pramoonjago P; Lyrawati D; Marzuki S
J Hum Genet; 2002; 47(11):594-604. PubMed ID: 12436196
[TBL] [Abstract][Full Text] [Related]
37. Visual function in chronic Leber's hereditary optic neuropathy during idebenone treatment initiated 5 to 50 years after onset.
Pemp B; Kircher K; Reitner A
Graefes Arch Clin Exp Ophthalmol; 2019 Dec; 257(12):2751-2757. PubMed ID: 31482278
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. A case of neuromyelitis optica harboring both anti-aquaporin-4 antibodies and a pathogenic mitochondrial DNA mutation for Leber's hereditary optic neuropathy.
Shiraishi W; Hayashi S; Kamada T; Isobe N; Yamasaki R; Murai H; Ohyagi Y; Kira J
Mult Scler; 2014 Feb; 20(2):258-60. PubMed ID: 24263387
[TBL] [Abstract][Full Text] [Related]
40. Juvenile open-angle Glaucoma associated with Leber's hereditary optic neuropathy: a case report and literature review.
Lin YH; Wang NK; Yeung L; Lai CC; Chuang LH
BMC Ophthalmol; 2018 Dec; 18(1):323. PubMed ID: 30558558
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]