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Journal Abstract Search

342 related items for PubMed ID: 16690316

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  • 5. [Penetrance of Leber hereditary optic neuropathy individuals with mitochondrial DNA 11778 mutation in the Shanxi area].
    Zheng ML, Zhang GL, Hua AL, Zhang YL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr; 21(2):166-7. PubMed ID: 15079802
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  • 10. Leber's optic neuropathy associated with disseminated white matter disease: a case report and review.
    Perez F, Anne O, Debruxelles S, Menegon P, Lambrecq V, Lacombe D, Martin-Negrier ML, Brochet B, Goizet C.
    Clin Neurol Neurosurg; 2009 Jan; 111(1):83-6. PubMed ID: 18848389
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  • 14. [A case or Leber hereditary optic neuropathy (LHON): differential diagnosis with post inflammatory atrophy of nerve II using the mtDNA analysis].
    Lubos L, Wajgt A, Maciejowski M, Mroczek-Tońska K, Bartnik E, Dziekanowska D.
    Neurol Neurochir Pol; 2003 Jan; 37(1):229-34. PubMed ID: 12910843
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  • 15. [Detection of mtDNA*LHON G11778A mutation by real-time polymerase chain reaction using TaqMan-MGB probe technology].
    Li YM, Wang JY, Chen Y, Shao JB, Wang J, Tong Y.
    Zhonghua Yan Ke Za Zhi; 2006 Aug; 42(8):728-32. PubMed ID: 17081446
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  • 19. 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; 30(1):171-4. PubMed ID: 16617593
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  • 20. 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
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