151 related articles for article (PubMed ID: 35146926)
1. 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; 100(7):797-804. PubMed ID: 35146926
[TBL] [Abstract][Full Text] [Related]
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
[TBL] [Abstract][Full Text] [Related]
3. 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
[TBL] [Abstract][Full Text] [Related]
4. 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):2672-2677. PubMed ID: 24120325
[TBL] [Abstract][Full Text] [Related]
5. 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
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 17724190
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 18653586
[TBL] [Abstract][Full Text] [Related]
8. 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
[TBL] [Abstract][Full Text] [Related]
9. Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy.
Votruba M; Thiselton D; Bhattacharya SS
Br J Ophthalmol; 2003 Jan; 87(1):48-53. PubMed ID: 12488262
[TBL] [Abstract][Full Text] [Related]
10. 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; 64(10):32. PubMed ID: 37498569
[TBL] [Abstract][Full Text] [Related]
11. 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; 34(1-2):69-74. PubMed ID: 22779427
[TBL] [Abstract][Full Text] [Related]
12. 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; 31(3):475-480. PubMed ID: 27858935
[TBL] [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; 351(1-2):99-108. PubMed ID: 25796301
[TBL] [Abstract][Full Text] [Related]
14. 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
[TBL] [Abstract][Full Text] [Related]
15. 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; 6(6):e21347. PubMed ID: 21731710
[TBL] [Abstract][Full Text] [Related]
16. Novel mutations in the OPA1 gene and associated clinical features in Japanese patients with optic atrophy.
Nakamura M; Lin J; Ueno S; Asaoka R; Hirai T; Hotta Y; Miyake Y; Terasaki H
Ophthalmology; 2006 Mar; 113(3):483-488.e1. PubMed ID: 16513463
[TBL] [Abstract][Full Text] [Related]
17. 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
[TBL] [Abstract][Full Text] [Related]
18. Autosomal dominant hereditary optic neuropathy (ADOA): a review of the genetics and clinical manifestations of ADOA and ADOA+.
Skidd PM; Lessell S; Cestari DM
Semin Ophthalmol; 2013; 28(5-6):422-6. PubMed ID: 24138050
[TBL] [Abstract][Full Text] [Related]
19. 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. PubMed ID: 17306754
[TBL] [Abstract][Full Text] [Related]
20. 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; 20():691-703. PubMed ID: 24883014
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]