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4. Leber's optic neuropathy and Charcot-Marie-Tooth disease. Report of a case. McCluskey DJ; O'Connor PS; Sheehy JT J Clin Neuroophthalmol; 1986 Jun; 6(2):76-81. PubMed ID: 2942573 [TBL] [Abstract][Full Text] [Related]
5. Difficulty differentiating Leber's from dominant optic neuropathy in a patient with remote visual loss. Jacobson DM; Stone EM J Clin Neuroophthalmol; 1991 Sep; 11(3):152-7. PubMed ID: 1836796 [TBL] [Abstract][Full Text] [Related]
6. [Leber's optic atrophy - an interdisciplinary study (author's transl)]. Müller-Jensen A; Bushart W; Steidinger J; Funk M; Hellner KA Klin Monbl Augenheilkd; 1978; 172(6):831-42. PubMed ID: 692018 [TBL] [Abstract][Full Text] [Related]
7. Ophthalmoscopic findings in Leber's hereditary optic neuropathy. II. The fundus findings in the affected family members. Nikoskelainen E; Hoyt WF; Nummelin K Arch Ophthalmol; 1983 Jul; 101(7):1059-68. PubMed ID: 6870629 [TBL] [Abstract][Full Text] [Related]
8. [Past, present, and future in Leber's hereditary optic neuropathy]. Oguchi Y Nippon Ganka Gakkai Zasshi; 2001 Dec; 105(12):809-27. PubMed ID: 11802455 [TBL] [Abstract][Full Text] [Related]
10. Peripapillary fluorescein leakage in 11778 Leber's optic neuropathy. Yen MY; Wei YH; Liu JH J Neuroophthalmol; 1996 Sep; 16(3):178-81. PubMed ID: 8865009 [TBL] [Abstract][Full Text] [Related]
11. Optic nerve sheath distention in Leber's optic neuropathy and the significance of the "Wallace mutation". Smith JL; Tse DT; Byrne SF; Johns DR; Stone EM J Clin Neuroophthalmol; 1990 Dec; 10(4):231-8. PubMed ID: 2150839 [TBL] [Abstract][Full Text] [Related]
12. Leber's hereditary optic neuroretinopathy (LHON) associated with mitochondrial DNA point mutation G11778A in two Croatian families. Martin-Kleiner I; Gabrilovac J; Bradvica M; Vidović T; Cerovski B; Fumić K; Boranić M Coll Antropol; 2006 Mar; 30(1):171-4. PubMed ID: 16617593 [TBL] [Abstract][Full Text] [Related]
16. [Clinical manifestation and molecular identification of patients with Leber's hereditary optic neuropathy in a national reference center for neuro-ophthalmology in Cuba]. Santiesteban-Freixas R; Rodríguez-Hernández M; Mendoza-Santiesteban CE; Carrero-Salgado M; Francisco-Plasencia M; Méndez-Larramendi I; Vidal-Casalís S; Rivero-Reyes R; Hirano M Rev Neurol; 1999 Sep 1-15; 29(5):408-15. PubMed ID: 10584242 [TBL] [Abstract][Full Text] [Related]
17. Stargardt's type maculopathy in a patient with 11778 Leber's optic neuropathy. Yen MY; Wei YH; Liu JH J Neuroophthalmol; 1996 Jun; 16(2):120-3. PubMed ID: 8797169 [TBL] [Abstract][Full Text] [Related]
19. A family with Charcot-Marie-Tooth disease and Leber's optic atrophy. McLeod JG; Low PA; Morgan JA Proc Aust Assoc Neurol; 1975; 12():23-5. PubMed ID: 1215391 [TBL] [Abstract][Full Text] [Related]
20. White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation. Lev D; Yanoov-Sharav M; Watemberg N; Leshinsky-Silver E; Lerman-Sagie T Eur J Paediatr Neurol; 2002; 6(2):121-3. PubMed ID: 11995959 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]