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Journal Abstract Search

724 related items for PubMed ID: 18676632

  • 1. Sporadic bilateral optic neuropathy in children: the role of mitochondrial abnormalities.
    Bosley TM, Brodsky MC, Glasier CM, Abu-Amero KK.
    Invest Ophthalmol Vis Sci; 2008 Dec; 49(12):5250-6. PubMed ID: 18676632
    [Abstract] [Full Text] [Related]

  • 2. Mitochondrial abnormalities in patients with LHON-like optic neuropathies.
    Abu-Amero KK, Bosley TM.
    Invest Ophthalmol Vis Sci; 2006 Oct; 47(10):4211-20. PubMed ID: 17003408
    [Abstract] [Full Text] [Related]

  • 3. Mitochondrial changes in leukocytes of patients with optic neuritis.
    Bosley TM, Constantinescu CS, Tench CR, Abu-Amero KK.
    Mol Vis; 2007 Aug 29; 13():1516-28. PubMed ID: 17893651
    [Abstract] [Full Text] [Related]

  • 4. Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations.
    Ferré M, Bonneau D, Milea D, Chevrollier A, Verny C, Dollfus H, Ayuso C, Defoort S, Vignal C, Zanlonghi X, Charlin JF, Kaplan J, Odent S, Hamel CP, Procaccio V, Reynier P, Amati-Bonneau P.
    Hum Mutat; 2009 Jul 29; 30(7):E692-705. PubMed ID: 19319978
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  • 5. Mitochondrial DNA content is decreased in autosomal dominant optic atrophy.
    Kim JY, Hwang JM, Ko HS, Seong MW, Park BJ, Park SS.
    Neurology; 2005 Mar 22; 64(6):966-72. PubMed ID: 15781809
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  • 7. Diagnostic potential of mitochondrial DNA assessment in patients with optic neuropathy.
    Feng X, Pu W, Gao D, Isashiki Y, Ohba N.
    Chin Med J (Engl); 2000 Aug 22; 113(8):743-6. PubMed ID: 11776061
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  • 8. Leber's hereditary optic neuropathy with childhood onset.
    Barboni P, Savini G, Valentino ML, La Morgia C, Bellusci C, De Negri AM, Sadun F, Carta A, Carbonelli M, Sadun AA, Carelli V.
    Invest Ophthalmol Vis Sci; 2006 Dec 22; 47(12):5303-9. PubMed ID: 17122117
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  • 9. Mitochondrial abnormalities in patients with primary open-angle glaucoma.
    Abu-Amero KK, Morales J, Bosley TM.
    Invest Ophthalmol Vis Sci; 2006 Jun 22; 47(6):2533-41. PubMed ID: 16723467
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  • 12. Mitochondrial disorder with OPA1 mutation lacking optic atrophy.
    Milone M, Younge BR, Wang J, Zhang S, Wong LJ.
    Mitochondrion; 2009 Jul 22; 9(4):279-81. PubMed ID: 19303950
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  • 15. [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
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  • 16. Leber hereditary optic neuropathy: mitochondrial mutations and degeneration of the optic nerve.
    Howell N.
    Vision Res; 1997 Dec 25; 37(24):3495-507. PubMed ID: 9425526
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  • 17. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes.
    Hofmann S, Bezold R, Jaksch M, Obermaier-Kusser B, Mertens S, Kaufhold P, Rabl W, Hecker W, Gerbitz KD.
    Genomics; 1997 Jan 01; 39(1):8-18. PubMed ID: 9027481
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  • 18. Hereditary optic neuropathies share a common mitochondrial coupling defect.
    Chevrollier A, Guillet V, Loiseau D, Gueguen N, de Crescenzo MA, Verny C, Ferre M, Dollfus H, Odent S, Milea D, Goizet C, Amati-Bonneau P, Procaccio V, Bonneau D, Reynier P.
    Ann Neurol; 2008 Jun 01; 63(6):794-8. PubMed ID: 18496845
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  • 19. Diagnostic genetic testing for patients with bilateral optic neuropathy and comparison of clinical features according to OPA1 mutation status.
    Gaier ED, Boudreault K, Nakata I, Janessian M, Skidd P, DelBono E, Allen KF, Pasquale LR, Place E, Cestari DM, Stacy RC, Rizzo JF, Wiggs JL.
    Mol Vis; 2017 Jun 01; 23():548-560. PubMed ID: 28848318
    [Abstract] [Full Text] [Related]

  • 20. Characterization of the mitochondrial genome in childhood multiple sclerosis. II. Multiple sclerosis without optic neuritis and LHON-associated genes.
    Wilichowski E, Ohlenbusch A, Hanefeld F.
    Neuropediatrics; 1998 Dec 01; 29(6):307-12. PubMed ID: 10029350
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