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5. Heterozygous deletion of the OPA1 gene in patients with dominant optic atrophy. Hayashi T; Sasano H; Katagiri S; Tsunoda K; Kameya S; Nakazawa M; Iwata T; Tsuneoka H Jpn J Ophthalmol; 2017 Sep; 61(5):395-401. PubMed ID: 28668999 [TBL] [Abstract][Full Text] [Related]
6. Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: a syndrome caused by a missense mutation in OPA1. Payne M; Yang Z; Katz BJ; Warner JE; Weight CJ; Zhao Y; Pearson ED; Treft RL; Hillman T; Kennedy RJ; Meire FM; Zhang K Am J Ophthalmol; 2004 Nov; 138(5):749-55. PubMed ID: 15531309 [TBL] [Abstract][Full Text] [Related]
7. Coenzyme Q10 therapy in hereditary motor sensory neuropathy type VI with novel mitofusin 2 mutation. Takahashi R; Ikeda T; Hamaguchi A; Iwasa K; Yamada M Intern Med; 2012; 51(7):791-3. PubMed ID: 22466841 [TBL] [Abstract][Full Text] [Related]
8. Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1. Lee J; Jung SC; Hong YB; Yoo JH; Koo H; Lee JH; Hong HD; Kim SB; Chung KW; Choi BO Mol Med Rep; 2016 Jul; 14(1):33-40. PubMed ID: 27150940 [TBL] [Abstract][Full Text] [Related]
9. Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy. Gallus GN; Cardaioli E; Rufa A; Da Pozzo P; Bianchi S; D'Eramo C; Collura M; Tumino M; Pavone L; Federico A Mol Vis; 2010 Feb; 16():178-83. PubMed ID: 20157369 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2. Züchner S; De Jonghe P; Jordanova A; Claeys KG; Guergueltcheva V; Cherninkova S; Hamilton SR; Van Stavern G; Krajewski KM; Stajich J; Tournev I; Verhoeven K; Langerhorst CT; de Visser M; Baas F; Bird T; Timmerman V; Shy M; Vance JM Ann Neurol; 2006 Feb; 59(2):276-81. PubMed ID: 16437557 [TBL] [Abstract][Full Text] [Related]
12. Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophy. Chalmers RM; Riordan-Eva P; Wood NW J Neurol Neurosurg Psychiatry; 1997 Apr; 62(4):385-7. PubMed ID: 9120454 [TBL] [Abstract][Full Text] [Related]
13. Exome sequencing identified a novel de novo OPA1 mutation in a consanguineous family presenting with optic atrophy. Cohen L; Tzur S; Goldenberg-Cohen N; Bormans C; Behar DM; Reinstein E Genet Res (Camb); 2016 Jun; 98():e10. PubMed ID: 27265430 [TBL] [Abstract][Full Text] [Related]
14. A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophy. Thiselton DL; Alexander C; Taanman JW; Brooks S; Rosenberg T; Eiberg H; Andreasson S; Van Regemorter N; Munier FL; Moore AT; Bhattacharya SS; Votruba M Invest Ophthalmol Vis Sci; 2002 Jun; 43(6):1715-24. PubMed ID: 12036970 [TBL] [Abstract][Full Text] [Related]
15. Dominant optic atrophy: correlation between clinical and molecular genetic studies. Puomila A; Huoponen K; Mäntyjärvi M; Hämäläinen P; Paananen R; Sankila EM; Savontaus ML; Somer M; Nikoskelainen E Acta Ophthalmol Scand; 2005 Jun; 83(3):337-46. PubMed ID: 15948788 [TBL] [Abstract][Full Text] [Related]
16. Hereditary motor and sensory neuropathy (HMSN) and optic atrophy (HMSN type VI, Vizioli). Weiller C; Ferbert A Eur Arch Psychiatry Clin Neurosci; 1991; 240(4-5):246-9. PubMed ID: 1647219 [TBL] [Abstract][Full Text] [Related]
17. A novel OPA1 mutation causing variable age of onset autosomal dominant optic atrophy plus in an Australian family. Ahmad KE; Davis RL; Sue CM J Neurol; 2015 Oct; 262(10):2323-8. PubMed ID: 26194196 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Electrophysiology and ocular blood flow in a family with dominant optic nerve atrophy and a mutation in the OPA1 gene. Gränse L; Bergstrand I; Thiselton D; Ponjavic V; Heijl A; Votruba M; Andréasson S Ophthalmic Genet; 2003 Dec; 24(4):233-45. PubMed ID: 14566653 [TBL] [Abstract][Full Text] [Related]
20. Multi-system neurological disease is common in patients with OPA1 mutations. Yu-Wai-Man P; Griffiths PG; Gorman GS; Lourenco CM; Wright AF; Auer-Grumbach M; Toscano A; Musumeci O; Valentino ML; Caporali L; Lamperti C; Tallaksen CM; Duffey P; Miller J; Whittaker RG; Baker MR; Jackson MJ; Clarke MP; Dhillon B; Czermin B; Stewart JD; Hudson G; Reynier P; Bonneau D; Marques W; Lenaers G; McFarland R; Taylor RW; Turnbull DM; Votruba M; Zeviani M; Carelli V; Bindoff LA; Horvath R; Amati-Bonneau P; Chinnery PF Brain; 2010 Mar; 133(Pt 3):771-86. PubMed ID: 20157015 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]