The natural history of OPA1-related autosomal dominant optic atrophyCOHN, A. C; TOOMES, C; HEWITT, A. W et al.British journal of ophthalmology. 2008, Vol 92, Num 10, pp 1333-1336, issn 0007-1161, 4 p.Article

Novel Mutations of the OPA1 Gene in Chinese Dominant Optic AtrophyYEN, May-Yung; WANG, An-Guor; LIN, Yen-Ching et al.Ophthalmology (Rochester, MN). 2010, Vol 117, Num 2, pp 392-396, issn 0161-6420, 5 p.Article

Short wavelength-automated perimetry compared with standard achromatic perimetry in autosomal dominant optic atrophyWALTERS, J. W; GAUME, A; PATE, L et al.British journal of ophthalmology. 2006, Vol 90, Num 10, pp 1267-1270, issn 0007-1161, 4 p.Article

OPA1, the disease gene for autosomal dominant optic atrophy, is specifically expressed in ganglion cells and intrinsic neurons of the retinaPESCH, Ulrike E. A; FRIES, Julia E; BETTE, Stefanie et al.Investigative ophthalmology & visual science. 2004, Vol 45, Num 11, pp 4217-4225, issn 0146-0404, 9 p.Article

Developmental expression profile of the optic atrophy gene product: OPA1 is not localized exclusively in the mammalian retinal ganglion cell layerAIJAZ, Saima; ERSKINE, Lynda; JEFFERY, Glen et al.Investigative ophthalmology & visual science. 2004, Vol 45, Num 6, pp 1667-1673, issn 0146-0404, 7 p.Article

Elevated Intraocular Pressure, Optic Nerve Atrophy, and Impaired Retinal Development in ODAG Transgenic MiceSASAKI, Takaaki; WATANABE, Wataru; SOUCHELNYTSKYI, Serhiy et al.Investigative ophthalmology & visual science. 2009, Vol 50, Num 1, pp 242-248, issn 0146-0404, 7 p.Article

Reduction of inner retinal thickness in patients with autosomal dominant optic atrophy associated with OPA1 mutationsITO, Yasuki; NAKAMURA, Makoto; YAMAKOSHI, Tomomi et al.Investigative ophthalmology & visual science. 2007, Vol 48, Num 9, pp 4079-4086, issn 0146-0404, 8 p.Article

Nouvelle mutation du gène OPA1 responsable d'une atrophie optique dominante isolée chez deux frères = A novel mutation of the OPA1 gene responsible for isolated autosomal dominant optic atrophy in two brothersMACAREZ, R; AMATI-BONNEAU, P; BURELLE, X et al.Journal français d'ophtalmologie. 2007, Vol 30, Num 2, pp 161-164, issn 0181-5512, 4 p.Article

The diagnostic yield of the evaluation for isolated unexplained optic atrophyLEE, Andrew G; CHAU, Felix Y; GOLNIK, Karl C et al.Ophthalmology (Rochester, MN). 2005, Vol 112, Num 5, pp 757-759, issn 0161-6420, 3 p.Article

Optical coherence tomography analysis of axonal loss in band atrophy of the optic nerveMONTEIRO, M. L. R; LEAL, B. C; ROSA, A. A. M et al.British journal of ophthalmology. 2004, Vol 88, Num 7, pp 896-899, issn 0007-1161, 4 p.Article

Evaluation of macular thickness measurements for detection of band atrophy of the optic nerve using optical coherence tomographyMOURA, Frederico C; MEDEIROS, Felipe A; MONTEIRO, Mario L. R et al.Ophthalmology (Rochester, MN). 2007, Vol 114, Num 1, pp 175-181, issn 0161-6420, 7 p.Article

Novel mutations in the OPA1 gene and associated clinical features in Japanese patients with optic atrophyNAKAMURA, Makoto; JIAN LIN; UENO, Shinji et al.Ophthalmology (Rochester, MN). 2006, Vol 113, Num 3, pp 483-488, issn 0161-6420, 6 p.Article

Is homelessness a risk factor for eye disease? : Results of a german screening studyPITZ, Susanne; KRAMANN, Christina; KRUMMENAUER, Frank et al.Ophthalmologica (Basel). 2005, Vol 219, Num 6, pp 345-349, issn 0030-3755, 5 p.Article

Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe macular and optic atrophyPERRAULT, Isabelle; HANEIN, Sylvain; EDELSON, Catherine et al.Nature genetics. 2012, Vol 44, Num 9, pp 975-977, issn 1061-4036, 3 p.Article

Defective Mitochondrial Adenosine Triphosphate Production in Skeletal Muscle From Patients With Dominant Optic Atrophy Due to OPA1 MutationsLODI, Raffaele; TONON, Caterina; WISSINGER, Bernd et al.Archives of neurology (Chicago). 2011, Vol 68, Num 1, pp 67-73, issn 0003-9942, 7 p.Article

Atrophie optique révélant une neurosyphilis = Optic atrophy revealing neurosyphilisHAJJAJ, Imane; KISSANI, Najib.La Presse médicale (1983). 2010, Vol 39, Num 7-8, pp 845-846, issn 0755-4982, 2 p.Article

Retrobulbar Optic Nerve Diameter Measured by High-Speed Magnetic Resonance Imaging as a Biomarker for Axonal Loss in Glaucomatous Optic AtrophyLAGREZE, Wolf A; GAGGL, Mirjam; WEIGEL, Matthias et al.Investigative ophthalmology & visual science. 2009, Vol 50, Num 9, pp 4223-4228, issn 0146-0404, 6 p.Article

TMEM126A, Encoding a Mitochondrial Protein, Is Mutated in Autosomal-Recessive Nonsyndromic Optic AtrophyHANEIN, Sylvain; PERRAULT, Isabelle; CHRETIEN, Dominique et al.American journal of human genetics. 2009, Vol 84, Num 4, pp 493-498, issn 0002-9297, 6 p.Article

Mitochondrial fragmentation in neurodegenerationKNOTT, Andrew B; PERKINS, Guy; SCHWARZENBACHER, Robert et al.Nature reviews. Neuroscience (Print). 2008, Vol 9, Num 7, pp 505-518, issn 1471-003X, 14 p.Article

PEHO and PEHO-like syndromes: Report of five Australian casesFIELD, M. J; GRATTAN-SMITH, P; PIPER, S. M et al.American journal of medical genetics. 2003, Vol 122A, Num 1, pp 6-12, issn 0148-7299, 7 p.Article

Early pericalcarine atrophy in acute optic neuritis is associated with conversion to multiple sclerosisJENKINS, T. M; CICCARELLI, O; ATZORI, M et al.Journal of neurology, neurosurgery and psychiatry. 2011, Vol 82, Num 9, pp 1017-1021, issn 0022-3050, 5 p.Article

Genomic rearrangements in OPA 1 are frequent in patients with autosomal dominant optic atrophyFUHRMANN, N; ALAVI, M. V; BITOUN, P et al.Journal of medical genetics. 2009, Vol 46, Num 2, pp 136-144, issn 0022-2593, 9 p.Article

MULTIPLE SCLEROSIS-LIKE DISORDER IN OPA1-RELATED AUTOSOMAL DOMINANT OPTIC ATROPHYVERNY, C; LOISEAU, D; BONNEAU, D et al.Neurology. 2008, Vol 70, Num 13, pp 1152-1153, issn 0028-3878, 2 p., 2Article

Macular thickness reduction in eyes with unilateral optic atrophy detected with optical coherence tomographyKUSUHARA, S; NAKAMURA, M; NAGAI-KUSUHARA, A et al.Eye (London. 1987). 2006, Vol 20, Num 8, pp 882-887, issn 0950-222X, 6 p.Article

OPA1 Deficiency Associated with Increased Autophagy in Retinal Ganglion Cells in a Murine Model of Dominant Optic AtrophyWHITE, Kathryn E; DAVIES, Vanessa J; HOGAN, Vanessa E et al.Investigative ophthalmology & visual science. 2009, Vol 50, Num 6, pp 2567-2571, issn 0146-0404, 5 p.Article