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Items: 1 to 20 of 203

1.

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. doi: 10.1111/aos.12378. Epub 2014 Mar 11.

2.

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. doi: 10.1111/aos.12835. Epub 2015 Sep 19.

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;120(12):2672-7. doi: 10.1016/j.ophtha.2013.08.008. Epub 2013 Oct 10.

PMID:
24120325
4.

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;48(9):4079-86.

PMID:
17724190
5.

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;2013:121398. doi: 10.1155/2013/121398. Epub 2013 Aug 19.

6.

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;88(3):342-6. doi: 10.1111/j.1755-3768.2008.01469.x. Epub 2009 Mar 19.

7.

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 Mar-Jun;34(1-2):69-74. doi: 10.3109/13816810.2012.702259. Epub 2012 Jul 11.

PMID:
22779427
8.
9.

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;251(1):221-34. doi: 10.1007/s00417-012-2112-7. Epub 2012 Aug 4.

PMID:
22865259
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;48(2):820-4.

PMID:
17251483
11.

Early macular retinal ganglion cell loss in dominant optic atrophy: genotype-phenotype correlation.

Barboni P, Savini G, Cascavilla ML, Caporali L, Milesi J, Borrelli E, La Morgia C, Valentino ML, Triolo G, Lembo A, Carta A, De Negri A, Sadun F, Rizzo G, Parisi V, Pierro L, Bianchi Marzoli S, Zeviani M, Sadun AA, Bandello F, Carelli V.

Am J Ophthalmol. 2014 Sep;158(3):628-36.e3. doi: 10.1016/j.ajo.2014.05.034. Epub 2014 Jun 5.

PMID:
24907432
12.

Optical coherence tomography shows early loss of the inferior temporal quadrant retinal nerve fiber layer in autosomal dominant optic atrophy.

Park SW, Hwang JM.

Graefes Arch Clin Exp Ophthalmol. 2015 Jan;253(1):135-41. doi: 10.1007/s00417-014-2852-7. Epub 2014 Nov 19.

PMID:
25408424
13.

The natural history of OPA1-related autosomal dominant optic atrophy.

Cohn AC, Toomes C, Hewitt AW, Kearns LS, Inglehearn CF, Craig JE, Mackey DA.

Br J Ophthalmol. 2008 Oct;92(10):1333-6. doi: 10.1136/bjo.2007.134726. Epub 2008 Jul 24.

PMID:
18653586
14.

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. doi: 10.1016/j.jns.2015.02.047. Epub 2015 Mar 6.

PMID:
25796301
15.

A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy.

Alavi MV, Bette S, Schimpf S, Schuettauf F, Schraermeyer U, Wehrl HF, Ruttiger L, Beck SC, Tonagel F, Pichler BJ, Knipper M, Peters T, Laufs J, Wissinger B.

Brain. 2007 Apr;130(Pt 4):1029-42. Epub 2007 Feb 21.

PMID:
17314202
16.

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;45(6):1667-73.

PMID:
15161824
17.

Autosomal dominant optic atrophy: penetrance and expressivity in patients with OPA1 mutations.

Cohn AC, Toomes C, Potter C, Towns KV, Hewitt AW, Inglehearn CF, Craig JE, Mackey DA.

Am J Ophthalmol. 2007 Apr;143(4):656-62. Epub 2007 Feb 15.

PMID:
17306754
18.

Retinal vessel diameter in normal-tension glaucoma patients with asymmetric progression.

Lee TE, Kim YY, Yoo C.

Graefes Arch Clin Exp Ophthalmol. 2014 Nov;252(11):1795-801. doi: 10.1007/s00417-014-2756-6. Epub 2014 Aug 12.

PMID:
25109787
19.

Opa1 deficiency in a mouse model of dominant optic atrophy leads to retinal ganglion cell dendropathy.

Williams PA, Morgan JE, Votruba M.

Brain. 2010 Oct;133(10):2942-51. doi: 10.1093/brain/awq218. Epub 2010 Sep 3.

PMID:
20817698
20.

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;94(7):e580-e585. doi: 10.1111/aos.12999. Epub 2016 Mar 3.

PMID:
26936288

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