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Journal Abstract Search
154 related items for PubMed ID: 24907432
1. 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. PubMed ID: 24907432 [Abstract] [Full Text] [Related]
2. Pattern of retinal ganglion cell loss in dominant optic atrophy due to OPA1 mutations. Yu-Wai-Man P, Bailie M, Atawan A, Chinnery PF, Griffiths PG. Eye (Lond); 2011 May; 25(5):596-602. PubMed ID: 21378995 [Abstract] [Full Text] [Related]
3. Optical Coherence Tomography of the Retinal Ganglion Cell Complex in Leber's Hereditary Optic Neuropathy and Dominant Optic Atrophy. Asanad S, Tian JJ, Frousiakis S, Jiang JP, Kogachi K, Felix CM, Fatemeh D, Irvine AG, Ter-Zakarian A, Falavarjani KG, Barboni P, Karanjia R, Sadun AA. Curr Eye Res; 2019 Jun; 44(6):638-644. PubMed ID: 30649972 [Abstract] [Full Text] [Related]
4. 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 [Abstract] [Full Text] [Related]
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. PubMed ID: 19302076 [Abstract] [Full Text] [Related]
7. 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 [Abstract] [Full Text] [Related]
8. 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 [Abstract] [Full Text] [Related]
9. 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 [Abstract] [Full Text] [Related]
10. AFG3L2 and ACO2-Linked Dominant Optic Atrophy: Genotype-Phenotype Characterization Compared to OPA1 Patients. Amore G, Romagnoli M, Carbonelli M, Cascavilla ML, De Negri AM, Carta A, Parisi V, Di Renzo A, Schiavi C, Lenzetti C, Zenesini C, Ormanbekova D, Palombo F, Fiorini C, Caporali L, Carelli V, Barboni P, La Morgia C. Am J Ophthalmol; 2024 Jun; 262():114-124. PubMed ID: 38278202 [Abstract] [Full Text] [Related]
11. 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 Jun; 2013():121398. PubMed ID: 24024178 [Abstract] [Full Text] [Related]
12. The Pattern of Retinal Ganglion Cell Loss in Wolfram Syndrome is Distinct From Mitochondrial Optic Neuropathies. Barboni P, Amore G, Cascavilla ML, Battista M, Frontino G, Romagnoli M, Caporali L, Baldoli C, Gramegna LL, Sessagesimi E, Bonfanti R, Romagnoli A, Scotti R, Brambati M, Carbonelli M, Starace V, Fiorini C, Panebianco R, Parisi V, Tonon C, Bandello F, Carelli V, La Morgia C. Am J Ophthalmol; 2022 Sep; 241():206-216. PubMed ID: 35452662 [Abstract] [Full Text] [Related]
13. Retinal dysfunction characterizes subtypes of dominant optic atrophy. Cascavilla ML, Parisi V, Triolo G, Ziccardi L, Borrelli E, Di Renzo A, Balducci N, Lamperti C, Bianchi Marzoli S, Darvizeh F, Sadun AA, Carelli V, Bandello F, Barboni P. Acta Ophthalmol; 2018 Mar; 96(2):e156-e163. PubMed ID: 28926202 [Abstract] [Full Text] [Related]
14. 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 [Abstract] [Full Text] [Related]
15. Ganglion cell loss in relation to visual disability in multiple sclerosis. Walter SD, Ishikawa H, Galetta KM, Sakai RE, Feller DJ, Henderson SB, Wilson JA, Maguire MG, Galetta SL, Frohman E, Calabresi PA, Schuman JS, Balcer LJ. Ophthalmology; 2012 Jun; 119(6):1250-7. PubMed ID: 22365058 [Abstract] [Full Text] [Related]
16. 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 Jun; 34(1-2):69-74. PubMed ID: 22779427 [Abstract] [Full Text] [Related]
17. Ganglion cell-inner plexiform layer thickness in patients with Parkinson disease and association with disease severity and duration. Sari ES, Koc R, Yazici A, Sahin G, Ermis SS. J Neuroophthalmol; 2015 Jun; 35(2):117-21. PubMed ID: 25485861 [Abstract] [Full Text] [Related]
18. 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. PubMed ID: 22865259 [Abstract] [Full Text] [Related]