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Journal Abstract Search

141 related items for PubMed ID: 8474822

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  • 8. Leber's hereditary optic neuropathy (LHON) with mitochondrial ND4 gene mutation (11778) in a Thai patient.
    Lertrit P, Ruangvaravate N, Trongpanich Y, Imsumran A, Mungkornkarn C, Neungton N.
    J Med Assoc Thai; 1999 Jan; 82(1):59-64. PubMed ID: 10087740
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  • 11. Evidence for a metabolic trigger for Leber's hereditary optic neuropathy. A case report.
    DuBois LG, Feldon SE.
    J Clin Neuroophthalmol; 1992 Mar; 12(1):15-6. PubMed ID: 1532594
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  • 13. 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 Mar; 6(2):121-3. PubMed ID: 11995959
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  • 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
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  • 15. [Analysis on the effect of secondary mutations on Leber's hereditary optic neuropathy].
    Wang Y, Tong Y, Hu SX, Wang JY, Shao JB, Zhang HX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):397-400. PubMed ID: 17680528
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  • 19. A family with Leber's hereditary optic neuropathy with mitochondrial DNA heteroplasmy related to disease expression.
    Tanaka A, Kiyosawa M, Mashima Y, Tokoro T.
    J Neuroophthalmol; 1998 Jun; 18(2):81-3. PubMed ID: 9621260
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  • 20. [A Mitochondrial mutation defect is identified in Leber's hereditary optic neuropathy].
    Ehinger B.
    Lakartidningen; 1989 Mar 29; 86(13):1161. PubMed ID: 2704272
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