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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

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

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

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

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

Secondary mtDNA Defects Do Not Cause Optic Nerve Dysfunction in a Mouse Model of Dominant Optic AtrophyYU-WAI-MAN, Patrick; DAVIES, Vanessa J; PIECHOTA, Malgorzata J et al.Investigative ophthalmology & visual science. 2009, Vol 50, Num 10, pp 4561-4566, issn 0146-0404, 6 p.Article

Pattern of retinal ganglion cell loss in dominant optic atrophy due to OPA1 mutations : GlaucomaYU-WAI-MAN, P; BAILIE, M; ATAWAN, A et al.Eye (London. 1987). 2011, Vol 25, Num 5, pp 596-602, issn 0950-222X, 7 p.Article

Retinal Nerve Fiber Layer Thickness in Dominant Optic Atrophy: Measurements by Optical Coherence Tomography and Correlation with AgeBARBONI, Piero; SAVINI, Giacomo; CARELLI, Valerio et al.Ophthalmology (Rochester, MN). 2011, Vol 118, Num 10, pp 2076-2080, issn 0161-6420, 5 p.Article

Neuroblastoma amplified sequence gene is associated with a novel short stature syndrome characterised by optic nerve atrophy and Pelger-Huët anomalyMAKSIMOVA, Nadezda; HARA, Kenju; NOGOVICINA, Anna et al.Journal of medical genetics. 2010, Vol 47, Num 8, pp 538-548, issn 0022-2593, 11 p.Article

Extra-medullary Hematopoiesis Causing Bilateral Optic Atrophy in Beta Thalassemia/Hb E DiseaseITTIPUNKUL, Nimitr; MARTIN, Tada; SIRIWANASAN, Rutchada et al.Chot Mai Het Thang Phaet. 2007, Vol 90, Num 4, pp 809-812, issn 0125-2208, 4 p.Article

LE SYNDROME DE WOLFRAM : À PROPOS DE QUATRE CASSKIKER, H; BOUTIMZINE, N; OUAZANI, B et al.Bulletin de la Société belge d'ophtalmologie. 2007, Num 306, pp 43-47, issn 0081-0746, 5 p.Article

Opa1 deficiency in a mouse model of dominant optic atrophy leads to retinal ganglion cell dendropathyWILLIAMS, Pete A; MORGAN, James E; VOTRUBA, Marcela et al.Brain. 2010, Vol 133, pp 2942-2951, issn 0006-8950, 10 p., 10Article

Subtle neurological and metabolic abnormalities in an Opa1 mouse model of autosomal dominant optic atrophyALAVI, Marcel V; FUHRMANN, Nico; HUU PHUC NGUYEN et al.Experimental neurology (Print). 2009, Vol 220, Num 2, pp 404-409, issn 0014-4886, 6 p.Article

SYNDROME DE WOLFRAM : A PROPOS DE DEUX CAS FAMILIAUX = WOLFRAM SYNDROM ABOUT 2 FAMILY CASESZGHAL-MOKNI, I; NACEF, L; MALEK, I et al.Maghreb médical. 2008, Num 389, pp 141-142, issn 0330-258X, 2 p.Article

A missense mutation in the murine Opa3 gene models human Costeff syndrome. CommentaryZEVIANI, Massimo; DAVIES, Vanessa J; MOAT, Stuart J et al.Brain. 2008, Vol 131, issn 0006-8950, 314-317, 368-380 [17 p.], 2Article

A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55)SHIMAZAKI, Haruo; TAKIYAMA, Yoshihisa; FUKUDA, Yoko et al.Journal of medical genetics. 2012, Vol 49, Num 12, pp 777-784, issn 0022-2593, 8 p.Article

3D vs 2D qualitative and semiquantitative evaluation of the glaucomatous optic disc atrophy using computer-assisted stereophotographyLEHMANN, M. V; MARDIN, C. Y; MARTUS, P et al.Eye (London. 1987). 2008, Vol 22, Num 5, pp 628-635, issn 0950-222X, 8 p.Article