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Journal Abstract Search

159 related items for PubMed ID: 37498569

  • 41. [Case report on OCT findings in a patient with hereditary optic neuropathy and a patient with autosomal dominant optic atrophy].
    Schild AM, Fricke J, Liakopoulos S.
    Klin Monbl Augenheilkd; 2011 Jun; 228(6):565-8. PubMed ID: 21108168
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  • 42. Peripapillary and macular morpho-vascular changes in patients with genetic or clinical diagnosis of autosomal dominant optic atrophy: a case-control study.
    Martins A, Rodrigues TM, Soares M, Dolan MJ, Murta JN, Silva R, Marques JP.
    Graefes Arch Clin Exp Ophthalmol; 2019 May; 257(5):1019-1027. PubMed ID: 30798343
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  • 43. Antisense Oligonucleotide STK-002 Increases OPA1 in Retina and Improves Mitochondrial Function in Autosomal Dominant Optic Atrophy Cells.
    Venkatesh A, McKenty T, Ali S, Sonntag D, Ravipaty S, Cui Y, Slate D, Lin Q, Christiansen A, Jacobson S, Kach J, Lim KH, Srinivasan V, Zinshteyn B, Aznarez I, Huryn LA, Li Z, Hufnagel RB, Liau G, Anderson K, Hoger J.
    Nucleic Acid Ther; 2024 Oct; 34(5):221-233. PubMed ID: 39264859
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  • 45. Pattern of retinal ganglion cell loss in dominant optic atrophy due to OPA1 mutations.
    Yu-Wai-Man P, Bailie M, Atawan A, Chinnery PF, Griffiths PG.
    Eye (Lond); 2011 May; 25(5):596-602. PubMed ID: 21378995
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  • 47. Genomic rearrangements in OPA1 are frequent in patients with autosomal dominant optic atrophy.
    Fuhrmann N, Alavi MV, Bitoun P, Woernle S, Auburger G, Leo-Kottler B, Yu-Wai-Man P, Chinnery P, Wissinger B.
    J Med Genet; 2009 Feb; 46(2):136-44. PubMed ID: 19181907
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  • 49. A novel ADOA-associated OPA1 mutation alters the mitochondrial function, membrane potential, ROS production and apoptosis.
    Zhang J, Liu X, Liang X, Lu Y, Zhu L, Fu R, Ji Y, Fan W, Chen J, Lin B, Yuan Y, Jiang P, Zhou X, Guan MX.
    Sci Rep; 2017 Jul 18; 7(1):5704. PubMed ID: 28720802
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  • 50. Autosomal dominant optic atrophy plus due to the novel OPA1 variant c.1463G>C.
    Finsterer J, Laccone F.
    Metab Brain Dis; 2019 Aug 18; 34(4):1023-1027. PubMed ID: 31152339
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  • 54. 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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  • 55. Multiethnic involvement in autosomal-dominant optic atrophy in Singapore.
    Loo JL, Singhal S, Rukmini AV, Tow S, Amati-Bonneau P, Procaccio V, Bonneau D, Gooley JJ, Reynier P, Ferré M, Milea D.
    Eye (Lond); 2017 Mar 20; 31(3):475-480. PubMed ID: 27858935
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  • 56. A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function.
    Spinazzi M, Cazzola S, Bortolozzi M, Baracca A, Loro E, Casarin A, Solaini G, Sgarbi G, Casalena G, Cenacchi G, Malena A, Frezza C, Carrara F, Angelini C, Scorrano L, Salviati L, Vergani L.
    Hum Mol Genet; 2008 Nov 01; 17(21):3291-302. PubMed ID: 18678599
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  • 57. Subtle neurological and metabolic abnormalities in an Opa1 mouse model of autosomal dominant optic atrophy.
    Alavi MV, Fuhrmann N, Nguyen HP, Yu-Wai-Man P, Heiduschka P, Chinnery PF, Wissinger B.
    Exp Neurol; 2009 Dec 01; 220(2):404-9. PubMed ID: 19815013
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  • 59. Does acute loss of vision in autosomal dominant optic atrophy occur early in childhood?
    Kearns LS, Forrest M, Cohn AC, Churchill AJ, Mackey DA.
    Ophthalmic Genet; 2010 Mar 01; 31(1):44-6. PubMed ID: 20141358
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