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86 related items for PubMed ID: 25186535

  • 21. Genomic deletions in OPA1 in Danish patients with autosomal dominant optic atrophy.
    Almind GJ, Grønskov K, Milea D, Larsen M, Brøndum-Nielsen K, Ek J.
    BMC Med Genet; 2011 Apr 04; 12():49. PubMed ID: 21457585
    [Abstract] [Full Text] [Related]

  • 22. Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families.
    Pretegiani E, Rosini F, Rufa A, Gallus GN, Cardaioli E, Da Pozzo P, Bianchi S, Serchi V, Collura M, Franceschini R, Bianchi Marzoli S, Dotti MT, Federico A.
    J Neurol Sci; 2017 Nov 15; 382():29-35. PubMed ID: 29111013
    [Abstract] [Full Text] [Related]

  • 23. Neuroradiological findings expand the phenotype of OPA1-related mitochondrial dysfunction.
    Roubertie A, Leboucq N, Picot MC, Nogue E, Brunel H, Le Bars E, Manes G, Angebault Prouteau C, Blanchet C, Mondain M, Chevassus H, Amati-Bonneau P, Sarzi E, Pagès M, Villain M, Meunier I, Lenaers G, Hamel CP.
    J Neurol Sci; 2015 Feb 15; 349(1-2):154-60. PubMed ID: 25641387
    [Abstract] [Full Text] [Related]

  • 24. 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 15; 46(2):136-44. PubMed ID: 19181907
    [Abstract] [Full Text] [Related]

  • 25. Mitochondrial oxidative phosphorylation compensation may preserve vision in patients with OPA1-linked autosomal dominant optic atrophy.
    Van Bergen NJ, Crowston JG, Kearns LS, Staffieri SE, Hewitt AW, Cohn AC, Mackey DA, Trounce IA.
    PLoS One; 2011 Feb 15; 6(6):e21347. PubMed ID: 21731710
    [Abstract] [Full Text] [Related]

  • 26. First report of OPA1 screening in Greek patients with autosomal dominant optic atrophy and identification of a previously undescribed OPA1 mutation.
    Kamakari S, Koutsodontis G, Tsilimbaris M, Fitsios A, Chrousos G.
    Mol Vis; 2014 Feb 15; 20():691-703. PubMed ID: 24883014
    [Abstract] [Full Text] [Related]

  • 27. Identification of copy number variation in the gene for autosomal dominant optic atrophy, OPA1, in a Chinese pedigree.
    Jin X, Chen YH, Liu Z, Deng Y, Li NN, Huang H, Qi M, Yi X, Zhu J.
    Genet Mol Res; 2015 Sep 21; 14(3):10961-72. PubMed ID: 26400325
    [Abstract] [Full Text] [Related]

  • 28. Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy.
    Votruba M, Thiselton D, Bhattacharya SS.
    Br J Ophthalmol; 2003 Jan 21; 87(1):48-53. PubMed ID: 12488262
    [Abstract] [Full Text] [Related]

  • 29. Fourteen novel OPA1 mutations in autosomal dominant optic atrophy including two de novo mutations in sporadic optic atrophy.
    Baris O, Delettre C, Amati-Bonneau P, Surget MO, Charlin JF, Catier A, Derieux L, Guyomard JL, Dollfus H, Jonveaux P, Ayuso C, Maumenee I, Lorenz B, Mohammed S, Tourmen Y, Bonneau D, Malthièry Y, Hamel C, Reynier P.
    Hum Mutat; 2003 Jun 21; 21(6):656. PubMed ID: 14961560
    [Abstract] [Full Text] [Related]

  • 30. 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 21; 31(3):475-480. PubMed ID: 27858935
    [Abstract] [Full Text] [Related]

  • 31. Assessment of macular function by microperimetry in unilateral resolved central serous chorioretinopathy.
    Ozdemir H, Karacorlu SA, Senturk F, Karacorlu M, Uysal O.
    Eye (Lond); 2008 Feb 21; 22(2):204-8. PubMed ID: 16936642
    [Abstract] [Full Text] [Related]

  • 32. High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy.
    Gallus GN, Cardaioli E, Rufa A, Collura M, Da Pozzo P, Pretegiani E, Tumino M, Pavone L, Federico A.
    Clin Genet; 2012 Sep 21; 82(3):277-82. PubMed ID: 21745197
    [Abstract] [Full Text] [Related]

  • 33. Short wavelength-automated perimetry compared with standard achromatic perimetry in autosomal dominant optic atrophy.
    Walters JW, Gaume A, Pate L.
    Br J Ophthalmol; 2006 Oct 21; 90(10):1267-70. PubMed ID: 16837542
    [Abstract] [Full Text] [Related]

  • 34. Fixation stability and macular light sensitivity in patients with diabetic maculopathy: a microperimetric study with a scanning laser ophthalmoscope.
    Kube T, Schmidt S, Toonen F, Kirchhof B, Wolf S.
    Ophthalmologica; 2005 Oct 21; 219(1):16-20. PubMed ID: 15627822
    [Abstract] [Full Text] [Related]

  • 35. 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 21; 37(4):624-630. PubMed ID: 35273349
    [Abstract] [Full Text] [Related]

  • 36. OPA1-associated disorders: phenotypes and pathophysiology.
    Amati-Bonneau P, Milea D, Bonneau D, Chevrollier A, Ferré M, Guillet V, Gueguen N, Loiseau D, de Crescenzo MA, Verny C, Procaccio V, Lenaers G, Reynier P.
    Int J Biochem Cell Biol; 2009 Oct 21; 41(10):1855-65. PubMed ID: 19389487
    [Abstract] [Full Text] [Related]

  • 37. Normative data set identifying properties of the macula across age groups: integration of visual function and retinal structure with microperimetry and spectral-domain optical coherence tomography.
    Sabates FN, Vincent RD, Koulen P, Sabates NR, Gallimore G.
    Retina; 2011 Oct 21; 31(7):1294-302. PubMed ID: 21358460
    [Abstract] [Full Text] [Related]

  • 38. Structural model of the OPA1 GTPase domain may explain the molecular consequences of a novel mutation in a family with autosomal dominant optic atrophy.
    Dadgar S, Hagens O, Dadgar SR, Haghighi EN, Schimpf S, Wissinger B, Garshasbi M.
    Exp Eye Res; 2006 Sep 21; 83(3):702-6. PubMed ID: 16698014
    [Abstract] [Full Text] [Related]

  • 39. Effects of OPA1 mutations on mitochondrial morphology and apoptosis: relevance to ADOA pathogenesis.
    Olichon A, Landes T, Arnauné-Pelloquin L, Emorine LJ, Mils V, Guichet A, Delettre C, Hamel C, Amati-Bonneau P, Bonneau D, Reynier P, Lenaers G, Belenguer P.
    J Cell Physiol; 2007 May 21; 211(2):423-30. PubMed ID: 17167772
    [Abstract] [Full Text] [Related]

  • 40. [Assessment of the macula function by static perimetry, microperimetry and rarebit perimetry in patients suffering from dry age related macular degeneration].
    Nowomiejska K, Oleszczuk A, Zubilewicz A, Krukowski J, Mańkowska A, Rejdak R, Zagórski Z.
    Klin Oczna; 2007 May 21; 109(4-6):131-4. PubMed ID: 17725269
    [Abstract] [Full Text] [Related]

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