396 related articles for article (PubMed ID: 24800637)
1. New MT-ND1 pathologic mutation for Leber hereditary optic neuropathy.
Martínez-Romero Í; Herrero-Martín MD; Llobet L; Emperador S; Martín-Navarro A; Narberhaus B; Ascaso FJ; López-Gallardo E; Montoya J; Ruiz-Pesini E
Clin Exp Ophthalmol; 2014 Dec; 42(9):856-64. PubMed ID: 24800637
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Mutations for Leber hereditary optic neuropathy in patients with alcohol and tobacco optic neuropathy.
Amaral-Fernandes MS; Marcondes AM; do Amor Divino Miranda PM; Maciel-Guerra AT; Sartorato EL
Mol Vis; 2011; 17():3175-9. PubMed ID: 22194643
[TBL] [Abstract][Full Text] [Related]
4. A MELAS-associated ND1 mutation causing leber hereditary optic neuropathy and spastic dystonia.
Spruijt L; Smeets HJ; Hendrickx A; Bettink-Remeijer MW; Maat-Kievit A; Schoonderwoerd KC; Sluiter W; de Coo IF; Hintzen RQ
Arch Neurol; 2007 Jun; 64(6):890-3. PubMed ID: 17562939
[TBL] [Abstract][Full Text] [Related]
5. Leber hereditary optic neuropathy due to a new ND1 mutation.
Soldath P; Wegener M; Sander B; Rosenberg T; Duno M; Wibrand F; Vissing J
Ophthalmic Genet; 2017; 38(5):480-485. PubMed ID: 28139165
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Mitochondrial DNA mutation m.3635G>A may be associated with Leber hereditary optic neuropathy in Chinese.
Zhang AM; Zou Y; Guo X; Jia X; Zhang Q; Yao YG
Biochem Biophys Res Commun; 2009 Aug; 386(2):392-5. PubMed ID: 19527690
[TBL] [Abstract][Full Text] [Related]
8. The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy.
Valentino ML; Barboni P; Ghelli A; Bucchi L; Rengo C; Achilli A; Torroni A; Lugaresi A; Lodi R; Barbiroli B; Dotti M; Federico A; Baruzzi A; Carelli V
Ann Neurol; 2004 Nov; 56(5):631-41. PubMed ID: 15505787
[TBL] [Abstract][Full Text] [Related]
9. Mild Leber hereditary optic neuropathy (LHON) in a Western European family due to the rare Asian m.14502T>C variant in the
Vandeputte J; Van Heetvelde M; Van Cauwenbergh C; Seneca S; De Baere E; Leroy BP; De Zaeytijd J
Ophthalmic Genet; 2021 Aug; 42(4):440-445. PubMed ID: 33858285
[TBL] [Abstract][Full Text] [Related]
10. Clinical, genetic, and biochemical characterization of a Leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations.
Brown MD; Allen JC; Van Stavern GP; Newman NJ; Wallace DC
Am J Med Genet; 2001 Dec; 104(4):331-8. PubMed ID: 11754070
[TBL] [Abstract][Full Text] [Related]
11. Assocation Between Leber's Hereditary Optic Neuropathy and MT-ND1 3460G>A Mutation-Induced Alterations in Mitochondrial Function, Apoptosis, and Mitophagy.
Zhang J; Ji Y; Chen J; Xu M; Wang G; Ci X; Lin B; Mo JQ; Zhou X; Guan MX
Invest Ophthalmol Vis Sci; 2021 Jul; 62(9):38. PubMed ID: 34311469
[TBL] [Abstract][Full Text] [Related]
12. Mitochondrial ND1 Variants in 1281 Chinese Subjects With Leber's Hereditary Optic Neuropathy.
Ji Y; Liang M; Zhang J; Zhu L; Zhang Z; Fu R; Liu X; Zhang M; Fu Q; Zhao F; Tong Y; Sun Y; Jiang P; Guan MX
Invest Ophthalmol Vis Sci; 2016 May; 57(6):2377-89. PubMed ID: 27177320
[TBL] [Abstract][Full Text] [Related]
13. Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy.
Ji Y; Zhang J; Yu J; Wang Y; Lu Y; Liang M; Li Q; Jin X; Wei Y; Meng F; Gao Y; Cang X; Tong Y; Liu X; Zhang M; Jiang P; Zhu T; Mo JQ; Huang T; Jiang P; Guan MX
Hum Mol Genet; 2019 May; 28(9):1515-1529. PubMed ID: 30597069
[TBL] [Abstract][Full Text] [Related]
14. Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis.
Kim JY; Hwang JM; Park SS
Ann Neurol; 2002 May; 51(5):630-4. PubMed ID: 12112111
[TBL] [Abstract][Full Text] [Related]
15. Previously Unclassified Mutation of mtDNA m.3472T>C: Evidence of Pathogenicity in Leber's Hereditary Optic Neuropathy.
Sheremet NL; Nevinitsyna TA; Zhorzholadze NV; Ronzina IA; Itkis YS; Krylova TD; Tsygankova PG; Malakhova VA; Zakharova EY; Tokarchuk AV; Panteleeva AA; Karger EM; Lyamzaev KG; Avetisov SE
Biochemistry (Mosc); 2016 Jul; 81(7):748-54. PubMed ID: 27449621
[TBL] [Abstract][Full Text] [Related]
16. Prevalence of the primary LHON mutations in Northern Finland associated with bilateral optic atrophy and tobacco-alcohol amblyopia.
Korkiamäki P; Kervinen M; Karjalainen K; Majamaa K; Uusimaa J; Remes AM
Acta Ophthalmol; 2013 Nov; 91(7):630-4. PubMed ID: 22970697
[TBL] [Abstract][Full Text] [Related]
17. Identification and characterization of a new pathologic mutation in a large Leber hereditary optic neuropathy pedigree.
Emperador S; Habbane M; López-Gallardo E; Del Rio A; Llobet L; Mateo J; Sanz-López AM; Fernández-García MJ; Sánchez-Tocino H; Benbunan-Ferreiro S; Calabuig-Goena M; Narvaez-Palazón C; Fernández-Vega B; González-Iglesias H; Urreizti R; Artuch R; Pacheu-Grau D; Bayona-Bafaluy P; Montoya J; Ruiz-Pesini E
Orphanet J Rare Dis; 2024 Apr; 19(1):148. PubMed ID: 38582886
[TBL] [Abstract][Full Text] [Related]
18. A family with 3460G>A and 11778G>A mutations and haplogroup analysis of Polish Leber hereditary optic neuropathy patients.
Tonska K; Kurzawa M; Ambroziak AM; Korwin-Rujna M; Szaflik JP; Grabowska E; Szaflik J; Bartnik E
Mitochondrion; 2008 Dec; 8(5-6):383-8. PubMed ID: 18801464
[TBL] [Abstract][Full Text] [Related]
19. Long-term screening for primary mitochondrial DNA variants associated with Leber hereditary optic neuropathy: incidence, penetrance and clinical features.
Marotta R; Chin J; Chiotis M; Shuey N; Collins SJ
Mitochondrion; 2020 Sep; 54():128-132. PubMed ID: 32861874
[TBL] [Abstract][Full Text] [Related]
20. Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON).
Peron C; Mauceri R; Cabassi T; Segnali A; Maresca A; Iannielli A; Rizzo A; Sciacca FL; Broccoli V; Carelli V; Tiranti V
Stem Cell Res; 2020 Oct; 48():101939. PubMed ID: 32771908
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
