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Journal Abstract Search


135 related items for PubMed ID: 20141358

  • 21. 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
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  • 24. 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
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  • 25. [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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  • 26. Difficulty differentiating Leber's from dominant optic neuropathy in a patient with remote visual loss.
    Jacobson DM, Stone EM.
    J Clin Neuroophthalmol; 1991 Sep 25; 11(3):152-7. PubMed ID: 1836796
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  • 33. Optic disc evaluation in optic neuropathies: the optic disc assessment project.
    O'Neill EC, Danesh-Meyer HV, Kong GX, Hewitt AW, Coote MA, Mackey DA, Crowston JG, Optic Nerve Study Group.
    Ophthalmology; 2011 May 25; 118(5):964-70. PubMed ID: 21126771
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  • 34. [How to distinguish between autosomal dominant optic atrophy and Leber's hereditary optic neuropathy].
    Leo-Kottler B, Jägle H, Küpker T, Schimpf S.
    Ophthalmologe; 2007 Dec 25; 104(12):1060-5. PubMed ID: 17899121
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  • 35. Electrophysiology and ocular blood flow in a family with dominant optic nerve atrophy and a mutation in the OPA1 gene.
    Gränse L, Bergstrand I, Thiselton D, Ponjavic V, Heijl A, Votruba M, Andréasson S.
    Ophthalmic Genet; 2003 Dec 25; 24(4):233-45. PubMed ID: 14566653
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  • 36. Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutation.
    Stone EM, Newman NJ, Miller NR, Johns DR, Lott MT, Wallace DC.
    J Clin Neuroophthalmol; 1992 Mar 25; 12(1):10-4. PubMed ID: 1532593
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  • 37. OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background.
    Pierron D, Ferré M, Rocher C, Chevrollier A, Murail P, Thoraval D, Amati-Bonneau P, Reynier P, Letellier T.
    BMC Med Genet; 2009 Jul 20; 10():70. PubMed ID: 19619285
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  • 38. Leber's hereditary optic neuropathy.
    Letchavanakul A, Dechphongsaphilas W, Dhamcharee V.
    J Med Assoc Thai; 1999 Oct 20; 82(10):1051-5. PubMed ID: 10561972
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  • 39. Bilateral vision loss due to Leber's hereditary optic neuropathy after long-term alcohol, nicotine and drug abuse.
    Maass J, Matthé E.
    Doc Ophthalmol; 2018 Apr 20; 136(2):145-153. PubMed ID: 29372350
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  • 40. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28.
    Alexander C, Votruba M, Pesch UE, Thiselton DL, Mayer S, Moore A, Rodriguez M, Kellner U, Leo-Kottler B, Auburger G, Bhattacharya SS, Wissinger B.
    Nat Genet; 2000 Oct 20; 26(2):211-5. PubMed ID: 11017080
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