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159 related items for PubMed ID: 37498569

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Reduction of inner retinal thickness in patients with autosomal dominant optic atrophy associated with OPA1 mutations.
    Ito Y, Nakamura M, Yamakoshi T, Lin J, Yatsuya H, Terasaki H.
    Invest Ophthalmol Vis Sci; 2007 Sep 03; 48(9):4079-86. PubMed ID: 17724190
    [Abstract] [Full Text] [Related]

  • 3. Imaging of the macula indicates early completion of structural deficit in autosomal-dominant optic atrophy.
    Rönnbäck C, Milea D, Larsen M.
    Ophthalmology; 2013 Dec 03; 120(12):2672-2677. PubMed ID: 24120325
    [Abstract] [Full Text] [Related]

  • 4. 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 03; 96(3):251-256. PubMed ID: 29091347
    [Abstract] [Full Text] [Related]

  • 5. 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 03; 93(8):762-6. PubMed ID: 26385429
    [Abstract] [Full Text] [Related]

  • 6. 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 03; 92(7):670-4. PubMed ID: 24612963
    [Abstract] [Full Text] [Related]

  • 7. SDOCT thickness measurements of various retinal layers in patients with autosomal dominant optic atrophy due to OPA1 mutations.
    Schild AM, Ristau T, Fricke J, Neugebauer A, Kirchhof B, Sadda SR, Liakopoulos S.
    Biomed Res Int; 2013 Nov 03; 2013():121398. PubMed ID: 24024178
    [Abstract] [Full Text] [Related]

  • 8. Correlation between visual acuity and OCT-measured retinal nerve fiber layer thickness in a family with ADOA and an OPA1 mutation.
    Russo A, Delcassi L, Marchina E, Semeraro F.
    Ophthalmic Genet; 2013 Nov 03; 34(1-2):69-74. PubMed ID: 22779427
    [Abstract] [Full Text] [Related]

  • 9. Assessment of the retinal posterior pole in dominant optic atrophy by spectral-domain optical coherence tomography and microperimetry.
    Cesareo M, Ciuffoletti E, Martucci A, Sebastiani J, Sorge RP, Lamantea E, Garavaglia B, Ricci F, Cusumano A, Nucci C, Brancati F.
    PLoS One; 2017 Nov 03; 12(3):e0174560. PubMed ID: 28358911
    [Abstract] [Full Text] [Related]

  • 10. Reduction of oscillatory potentials and photopic negative response in patients with autosomal dominant optic atrophy with OPA1 mutations.
    Miyata K, Nakamura M, Kondo M, Lin J, Ueno S, Miyake Y, Terasaki H.
    Invest Ophthalmol Vis Sci; 2007 Feb 03; 48(2):820-4. PubMed ID: 17251483
    [Abstract] [Full Text] [Related]

  • 11. Optical coherence tomography angiography in the multimodal assessment of the retinal posterior pole in autosomal dominant optic atrophy.
    Cesareo M, Giannini C, Di Marino M, Aloe G, Martucci A, Aiello F, Cusumano A, Mancino R, Ricci F, Sorge RP, Nucci C.
    Acta Ophthalmol; 2022 May 03; 100(3):e798-e806. PubMed ID: 34250739
    [Abstract] [Full Text] [Related]

  • 12. Physiological evidence for impairment in autosomal dominant optic atrophy at the pre-ganglion level.
    Reis A, Mateus C, Viegas T, Florijn R, Bergen A, Silva E, Castelo-Branco M.
    Graefes Arch Clin Exp Ophthalmol; 2013 Jan 03; 251(1):221-34. PubMed ID: 22865259
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. Developmental expression profile of the optic atrophy gene product: OPA1 is not localized exclusively in the mammalian retinal ganglion cell layer.
    Aijaz S, Erskine L, Jeffery G, Bhattacharya SS, Votruba M.
    Invest Ophthalmol Vis Sci; 2004 Jun 15; 45(6):1667-73. PubMed ID: 15161824
    [Abstract] [Full Text] [Related]

  • 15. Comparison of the clinical and genetic features of autosomal dominant optic atrophy and normal tension glaucoma in young Chinese adults.
    Zhang Y, Sun X, Tian G, Chen Y.
    Eye (Lond); 2023 Mar 15; 37(4):624-630. PubMed ID: 35273349
    [Abstract] [Full Text] [Related]

  • 16. Vision-related quality of life and visual ability in patients with autosomal dominant optic atrophy.
    Eckmann-Hansen C, Bek T, Sander B, Larsen M.
    Acta Ophthalmol; 2022 Nov 15; 100(7):797-804. PubMed ID: 35146926
    [Abstract] [Full Text] [Related]

  • 17. Macular sensitivity and fixation patterns in patients with autosomal dominant optic atrophy.
    Rönnbäck C, Larsen M.
    Dan Med J; 2014 Sep 15; 61(9):A4888. PubMed ID: 25186535
    [Abstract] [Full Text] [Related]

  • 18. Prevalence of Macular Microcystoid Lacunae in Autosomal Dominant Optic Atrophy Assessed With Adaptive Optics.
    Eckmann-Hansen C, Bek T, Sander B, Grønskov K, Larsen M.
    J Neuroophthalmol; 2022 Sep 01; 42(3):328-333. PubMed ID: 35439206
    [Abstract] [Full Text] [Related]

  • 19. Genomics combined with a protein informatics platform to assess a novel pathogenic variant c.1024 A>G (p.K342E) in OPA1 in a patient with autosomal dominant optic atrophy.
    Ahuja AS, Selvam P, Vadlamudi C, Chopra H, Richter JE, Macklin SK, Samreen A, Helmi H, Mohammaad AN, Hines S, Davila MC, Atwal PS, Caulfield TR.
    Ophthalmic Genet; 2020 Dec 01; 41(6):563-569. PubMed ID: 32940104
    [Abstract] [Full Text] [Related]

  • 20. 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 01; 46():262-269. PubMed ID: 30165240
    [Abstract] [Full Text] [Related]

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