These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 36143917)

  • 1. Relative Leukocyte Telomere Length and Telomerase Complex Regulatory Markers Association with Leber's Hereditary Optic Neuropathy.
    Liutkeviciene R; Mikalauskaite R; Gedvilaite G; Glebauskiene B; Kriauciuniene L; Žemaitienė R
    Medicina (Kaunas); 2022 Sep; 58(9):. PubMed ID: 36143917
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Evaluation of Mitochondrial Dysfunction and Idebenone Responsiveness in Fibroblasts from Leber's Hereditary Optic Neuropathy (LHON) Subjects.
    Baglivo M; Nasca A; Lamantea E; Vinci S; Spagnolo M; Marchet S; Prokisch H; Catania A; Lamperti C; Ghezzi D
    Int J Mol Sci; 2023 Aug; 24(16):. PubMed ID: 37628761
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [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]  

  • 5. Pathogenic mitochondrial DNA mutations and associated clinical features in Korean patients with Leber's hereditary optic neuropathy.
    Yum HR; Chae H; Shin SY; Kim Y; Kim M; Park SH
    Invest Ophthalmol Vis Sci; 2014 Oct; 55(12):8095-101. PubMed ID: 25342614
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Leber's hereditary optic neuropathy - Case report.
    Iorga RE; Mihailovici R; Ozturk MR; Costin D
    Rom J Ophthalmol; 2018; 62(1):64-71. PubMed ID: 29796436
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. [DNA diagnosis in the age of individual made-to-order medications].
    Mashima Y
    Nippon Ganka Gakkai Zasshi; 2004 Dec; 108(12):863-85; discussion 886. PubMed ID: 15656090
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Increased 8-hydroxy-2'-deoxyguanosine in leukocyte DNA in Leber's hereditary optic neuropathy.
    Yen MY; Kao SH; Wang AG; Wei YH
    Invest Ophthalmol Vis Sci; 2004 Jun; 45(6):1688-91. PubMed ID: 15161827
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Leber's hereditary optic neuropathy clinical features in patients with mitochondrial DNA m.13513G>A candidate mutation].
    Andreeva NA; Murakhovskaya YK; Tsygankova PG; Krilova TD; Sheremet NL
    Vestn Oftalmol; 2022; 138(5. Vyp. 2):208-214. PubMed ID: 36287157
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of novel mitochondrial mutations in Leber's hereditary optic neuropathy.
    Kumar M; Tanwar M; Saxena R; Sharma P; Dada R
    Mol Vis; 2010 Apr; 16():782-92. PubMed ID: 20454697
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Whole mitochondrial genome analysis in South Indian patients with Leber's hereditary optic neuropathy.
    Saikia BB; Dubey SK; Shanmugam MK; Sundaresan P
    Mitochondrion; 2017 Sep; 36():21-28. PubMed ID: 27989883
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characteristics of Japanese patients with Leber's hereditary optic neuropathy and idebenone trial: a prospective, interventional, non-comparative study.
    Ishikawa H; Masuda Y; Ishikawa H; Shikisima K; Goseki T; Kezuka T; Terao M; Miyazaki A; Matsumoto K; Nishikawa H; Gomi F; Mimura O
    Jpn J Ophthalmol; 2021 Jan; 65(1):133-142. PubMed ID: 33185792
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Candidate Modifier Genes for the Penetrance of Leber's Hereditary Optic Neuropathy.
    Cheng HC; Chi SC; Liang CY; Yu JY; Wang AG
    Int J Mol Sci; 2022 Oct; 23(19):. PubMed ID: 36233195
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association of optic disc size with development and prognosis of Leber's hereditary optic neuropathy.
    Ramos Cdo V; Bellusci C; Savini G; Carbonelli M; Berezovsky A; Tamaki C; Cinoto R; Sacai PY; Moraes-Filho MN; Miura HM; Valentino ML; Iommarini L; De Negri AM; Sadun F; Cortelli P; Montagna P; Salomao SR; Sadun AA; Carelli V; Barboni P
    Invest Ophthalmol Vis Sci; 2009 Apr; 50(4):1666-74. PubMed ID: 19098324
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Leber's hereditary optic neuropathy--two case reports].
    Mulak M; Kisza K; Dembska K; Misiuk-Hojło M
    Klin Oczna; 2013; 115(3):238-41. PubMed ID: 24741932
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Colour vision defects in asymptomatic carriers of the Leber's hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case-control study.
    Quiros PA; Torres RJ; Salomao S; Berezovsky A; Carelli V; Sherman J; Sadun F; De Negri A; Belfort R; Sadun AA
    Br J Ophthalmol; 2006 Feb; 90(2):150-3. PubMed ID: 16424523
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The telomerase gene polymorphisms, but not telomere length, increase susceptibility to primary glomerulonephritis/end stage renal diseases in females.
    Sun Q; Liu J; Cheng G; Dai M; Liu J; Qi Z; Zhao J; Li W; Kong F; Liu G; Björkholm M; Xu D
    J Transl Med; 2020 May; 18(1):184. PubMed ID: 32366311
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.