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29. A Case of Atypical Leber Hereditary Optic Neuropathy With Slow, Symmetrical Progression Over Three Years. Chun BY; Kim DW; Son BJ J Neuroophthalmol; 2018 Sep; 38(3):421-422. PubMed ID: 30106804 [No Abstract] [Full Text] [Related]
30. Never too old: late-onset Leber hereditary optic neuropathy. Vincent SJ; Lowe KA; Monsour CS Clin Exp Optom; 2018 Jan; 101(1):137-139. PubMed ID: 28281297 [No Abstract] [Full Text] [Related]
31. Seven-Year Follow-up of Gene Therapy for Leber's Hereditary Optic Neuropathy. Yuan J; Zhang Y; Liu H; Wang D; Du Y; Tian Z; Li X; Yang S; Pei H; Wan X; Xiao S; Song L; Xiao X; Sun J; Wang Z; Li B Ophthalmology; 2020 Aug; 127(8):1125-1127. PubMed ID: 32284191 [No Abstract] [Full Text] [Related]
32. A Middle-aged Woman With Vision Loss and Cecocentral Scotoma. Jacobi JE; Leavitt JA; Chen JJ JAMA Ophthalmol; 2018 Sep; 136(9):1070-1071. PubMed ID: 29955763 [No Abstract] [Full Text] [Related]
33. Leber Hereditary Optic Neuropathy: Bringing the Lab to the Clinic. Rasool N; Lessell S; Cestari DM Semin Ophthalmol; 2016; 31(1-2):107-16. PubMed ID: 26959136 [TBL] [Abstract][Full Text] [Related]
34. Infantile Presentation of Leber Hereditary Optic Neuropathy "Plus" Disease. Zakrzewski H; Modabber M; Wilson N; Al-Hertani W; Toffoli D J Neuroophthalmol; 2019 Jun; 39(2):249-252. PubMed ID: 30829945 [No Abstract] [Full Text] [Related]
36. Prevalence of the primary LHON mutations in Northern Finland associated with bilateral optic atrophy and tobacco-alcohol amblyopia. Korkiamäki P; Kervinen M; Karjalainen K; Majamaa K; Uusimaa J; Remes AM Acta Ophthalmol; 2013 Nov; 91(7):630-4. PubMed ID: 22970697 [TBL] [Abstract][Full Text] [Related]
37. [A case or Leber hereditary optic neuropathy (LHON): differential diagnosis with post inflammatory atrophy of nerve II using the mtDNA analysis]. Lubos L; Wajgt A; Maciejowski M; Mroczek-Tońska K; Bartnik E; Dziekanowska D Neurol Neurochir Pol; 2003; 37(1):229-34. PubMed ID: 12910843 [TBL] [Abstract][Full Text] [Related]
38. Atypical Leber Hereditary Optic Neuropathy: 18 Year Interval Between Eyes. Ohden KL; Tang PH; Lilley CC; Lee MS J Neuroophthalmol; 2016 Sep; 36(3):304. PubMed ID: 26819093 [TBL] [Abstract][Full Text] [Related]
39. An uncommon cause of vision loss: Leber hereditary optic neuropathy. Glover JM; Casmaer ML; April MD JAAPA; 2018 Nov; 31(11):32-34. PubMed ID: 30358677 [TBL] [Abstract][Full Text] [Related]
40. Central retinal vein occlusion as the initial manifestation of LHON / MELAS overlap syndrome with mitochondrial DNA G13513A mutation--case report and literature review. Hsieh YT; Yang MT; Peng YJ; Hsu WC Ophthalmic Genet; 2011 Mar; 32(1):31-8. PubMed ID: 21174521 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]