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433 related items for PubMed ID: 11961321

  • 1. Leber's hereditary optic neuropathy with 3460 mitochondrial DNA mutation.
    Hwang JM, Chang BL, Koh HJ, Kim JY, Park SS.
    J Korean Med Sci; 2002 Apr; 17(2):283-6. PubMed ID: 11961321
    [Abstract] [Full Text] [Related]

  • 2. Lack of association between Leber's hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran.
    Houshmand M, Sanati MH, Rashedi I, Sharifpanah F, Asghari E, Lotfi J.
    Eur Neurol; 2004 Apr; 51(2):68-71. PubMed ID: 14671420
    [Abstract] [Full Text] [Related]

  • 3. [Past, present, and future in Leber's hereditary optic neuropathy].
    Oguchi Y.
    Nippon Ganka Gakkai Zasshi; 2001 Dec; 105(12):809-27. PubMed ID: 11802455
    [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
    [Abstract] [Full Text] [Related]

  • 5. White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation.
    Lev D, Yanoov-Sharav M, Watemberg N, Leshinsky-Silver E, Lerman-Sagie T.
    Eur J Paediatr Neurol; 2002 May; 6(2):121-3. PubMed ID: 11995959
    [Abstract] [Full Text] [Related]

  • 6.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Yu-Wai-Man P, Chinnery PF.
    ; 1993 May. PubMed ID: 20301353
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Case report: A Thai patient with Leber's hereditary optic neuropathy linked to mitochondrial DNA 14484 mutation.
    Chuenkongkaew W, Lertrit P, Suphavilai R.
    Southeast Asian J Trop Med Public Health; 2004 Mar; 35(1):167-8. PubMed ID: 15272763
    [Abstract] [Full Text] [Related]

  • 9. Leber's hereditary optic neuropathy mutations in ethambutol-induced optic neuropathy.
    Hwang JM, Kim J, Park SS.
    J Neurol; 2003 Jan; 250(1):87-9. PubMed ID: 12527998
    [Abstract] [Full Text] [Related]

  • 10. Leber's hereditary optic neuropathy with the 3434, 9011 mitochondrial DNA point mutation.
    Shidara K, Wakakura M.
    Jpn J Ophthalmol; 2012 Mar; 56(2):175-80. PubMed ID: 22183138
    [Abstract] [Full Text] [Related]

  • 11. Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation--A case report.
    Grazina MM, Diogo LM, Garcia PC, Silva ED, Garcia TD, Robalo CB, Oliveira CR.
    Eur J Paediatr Neurol; 2007 Mar; 11(2):115-8. PubMed ID: 17254817
    [Abstract] [Full Text] [Related]

  • 12. [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
    [Abstract] [Full Text] [Related]

  • 13. Leber's hereditary optic neuropathy mutations in Korean patients with multiple sclerosis.
    Hwang JM, Chang BL, Park SS.
    Ophthalmologica; 2001 Mar; 215(6):398-400. PubMed ID: 11741103
    [Abstract] [Full Text] [Related]

  • 14. Mitochondrial DNA mutations in Korean patients with Leber's hereditary optic neuropathy.
    Yang HK, Seong MW, Hwang JM.
    Sci Rep; 2024 Mar 08; 14(1):5702. PubMed ID: 38459091
    [Abstract] [Full Text] [Related]

  • 15. 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 08; 30(1):171-4. PubMed ID: 16617593
    [Abstract] [Full Text] [Related]

  • 16. [Sudden blindness: consider Leber's hereditary optic neuropathy].
    Schieving JH, de Vries BB, Hol F, Stroink H.
    Ned Tijdschr Geneeskd; 2008 Oct 25; 152(43):2313-6. PubMed ID: 19024058
    [Abstract] [Full Text] [Related]

  • 17. Spectrum of the mitochondrial DNA mutations of Leber's hereditary optic neuropathy in Koreans.
    Kim JY, Hwang JM, Chang BL, Park SS.
    J Neurol; 2003 Mar 25; 250(3):278-81. PubMed ID: 12638016
    [Abstract] [Full Text] [Related]

  • 18. Leber's hereditary optic neuropathy masquerading as optic neuritis with spontaneous visual recovery.
    Hsu TK, Wang AG, Yen MY, Liu JH.
    Clin Exp Optom; 2014 Jan 25; 97(1):84-6. PubMed ID: 23905692
    [Abstract] [Full Text] [Related]

  • 19. 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 23; 55(12):8095-101. PubMed ID: 25342614
    [Abstract] [Full Text] [Related]

  • 20. 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 23; 15(Pt 2):183-8. PubMed ID: 11339587
    [Abstract] [Full Text] [Related]

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