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86 related items for PubMed ID: 25186535

  • 1. Macular sensitivity and fixation patterns in patients with autosomal dominant optic atrophy.
    Rönnbäck C, Larsen M.
    Dan Med J; 2014 Sep; 61(9):A4888. PubMed ID: 25186535
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  • 2. Retinal vessel diameters decrease with macular ganglion cell layer thickness in autosomal dominant optic atrophy and in healthy subjects.
    Rönnbäck C, Grønskov K, Larsen M.
    Acta Ophthalmol; 2014 Nov; 92(7):670-4. PubMed ID: 24612963
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  • 5. Thickness mapping of individual retinal layers and sectors by Spectralis SD-OCT in Autosomal Dominant Optic Atrophy.
    Corajevic N, Larsen M, Rönnbäck C.
    Acta Ophthalmol; 2018 May; 96(3):251-256. PubMed ID: 29091347
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  • 6. Genotype-phenotype heterogeneity of ganglion cell and inner plexiform layer deficit in autosomal-dominant optic atrophy.
    Rönnbäck C, Nissen C, Almind GJ, Grønskov K, Milea D, Larsen M.
    Acta Ophthalmol; 2015 Dec; 93(8):762-6. PubMed ID: 26385429
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  • 12. Meta-analysis of genotype-phenotype analysis of OPA1 mutations in autosomal dominant optic atrophy.
    Ham M, Han J, Osann K, Smith M, Kimonis V.
    Mitochondrion; 2019 May; 46():262-269. PubMed ID: 30165240
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  • 13. A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophy.
    Thiselton DL, Alexander C, Taanman JW, Brooks S, Rosenberg T, Eiberg H, Andreasson S, Van Regemorter N, Munier FL, Moore AT, Bhattacharya SS, Votruba M.
    Invest Ophthalmol Vis Sci; 2002 Jun; 43(6):1715-24. PubMed ID: 12036970
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  • 14. 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; 31(1):44-6. PubMed ID: 20141358
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  • 15. Analysis of opa1 isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 gene.
    Formichi P, Radi E, Giorgi E, Gallus GN, Brunetti J, Battisti C, Rufa A, Dotti MT, Franceschini R, Bracci L, Federico A.
    J Neurol Sci; 2015 Apr 15; 351(1-2):99-108. PubMed ID: 25796301
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  • 16. Axonal loss occurs early in dominant optic atrophy.
    Milea D, Sander B, Wegener M, Jensen H, Kjer B, Jørgensen TM, Lund-Andersen H, Larsen M.
    Acta Ophthalmol; 2010 May 15; 88(3):342-6. PubMed ID: 19302076
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  • 18. Visual Function and Inner Retinal Structure in Relation to Birth Factors in Autosomal Dominant Optic Atrophy.
    Eckmann-Hansen C, Bek T, Sander B, Larsen M.
    Invest Ophthalmol Vis Sci; 2023 Jul 03; 64(10):32. PubMed ID: 37498569
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  • 19. The reduction of temporal optic nerve head microcirculation in autosomal dominant optic atrophy.
    Inoue M, Himori N, Kunikata H, Takeshita T, Aizawa N, Shiga Y, Omodaka K, Nishiguchi KM, Takahashi H, Nakazawa T.
    Acta Ophthalmol; 2016 Nov 03; 94(7):e580-e585. PubMed ID: 26936288
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