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22. Clinical and biochemical findings in Leber's hereditary optic atrophy. Syme IG, Bronte-Stewart J, Foulds WS, McClure E, Logan R, Stansfield M. Trans Ophthalmol Soc U K (1962); 1983; 103 ( Pt 5)():556-9. PubMed ID: 6591596 [Abstract] [Full Text] [Related]
23. [A pedigree of Leber's hereditary optic neuropathy with mtDNA 14484 mutation]. Tong Y, Wang Y, Jiang F, Liu B, Zhang S, Yang W. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):531-3. PubMed ID: 18841565 [Abstract] [Full Text] [Related]
24. Visual and neural function in Leber's optic neuropathy. Kothe AC, Lovasik JV, Pace R, Hrynchak PK, Flanagan JG. Optom Vis Sci; 1990 Feb; 67(2):138-47. PubMed ID: 2336254 [Abstract] [Full Text] [Related]
25. The clinical findings in Leber's hereditary optic neuroretinopathy. Leber's disease. Nikoskelainen E. Trans Ophthalmol Soc U K (1962); 1985 Feb; 104 ( Pt 8)():845-52. PubMed ID: 3879564 [Abstract] [Full Text] [Related]
26. Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis. Kim JY, Hwang JM, Park SS. Ann Neurol; 2002 May; 51(5):630-4. PubMed ID: 12112111 [Abstract] [Full Text] [Related]
27. Papillitis as an onset sign of Leber's hereditary optic neuropathy: a case report. Pantaleoni C, D'Arrigo S, Bagnasco I, Piozzi E, Carrara F, Scaioli V, Riva D. Brain Dev; 2001 Mar; 23(2):125-7. PubMed ID: 11248462 [Abstract] [Full Text] [Related]
28. [A Mitochondrial mutation defect is identified in Leber's hereditary optic neuropathy]. Ehinger B. Lakartidningen; 1989 Mar 29; 86(13):1161. PubMed ID: 2704272 [No Abstract] [Full Text] [Related]
30. Leber's hereditary optic neuropathy (LHON) with mitochondrial ND4 gene mutation (11778) in a Thai patient. Lertrit P, Ruangvaravate N, Trongpanich Y, Imsumran A, Mungkornkarn C, Neungton N. J Med Assoc Thai; 1999 Jan 29; 82(1):59-64. PubMed ID: 10087740 [Abstract] [Full Text] [Related]
31. Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation. Shoffner JM, Brown MD, Stugard C, Jun AS, Pollock S, Haas RH, Kaufman A, Koontz D, Kim Y, Graham JR. Ann Neurol; 1995 Aug 29; 38(2):163-9. PubMed ID: 7654063 [Abstract] [Full Text] [Related]
32. Leber's hereditary optic neuropathy as a cause of severe visual loss in childhood. Moorman CM, Elston JS, Matthews P. Pediatrics; 1993 May 29; 91(5):988-9. PubMed ID: 8474822 [No Abstract] [Full Text] [Related]
33. [Leber's optic atrophy (case report of progressive hereditary amaurosis]. Bozić K, Filipović D, Krkljes M, Kelemen A, Ivetić V. Med Pregl; 1994 May 29; 47(1-2):62-4. PubMed ID: 7739437 [Abstract] [Full Text] [Related]
34. Leigh-like encephalopathy complicating Leber's hereditary optic neuropathy. Funalot B, Reynier P, Vighetto A, Ranoux D, Bonnefont JP, Godinot C, Malthièry Y, Mas JL. Ann Neurol; 2002 Sep 29; 52(3):374-7. PubMed ID: 12205655 [Abstract] [Full Text] [Related]
35. 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 Sep 29; 51(7):791-3. PubMed ID: 22466841 [Abstract] [Full Text] [Related]
36. [Amaurosis congenita (Leber) with severe genital developmental delay]. Fehlow P. Padiatr Grenzgeb; 1989 Sep 29; 28(4):237-40. PubMed ID: 2797836 [Abstract] [Full Text] [Related]
38. [Leber's hereditary optic neuropathy]. Konrádová V, Zeman J, Stratilová L, Hermanská J, Vseticka I, Misovicová N, Kurca E, Gerinec A, Houstĕk J. Cas Lek Cesk; 1999 Oct 20; 138(18):565-8. PubMed ID: 10596473 [Abstract] [Full Text] [Related]
39. Virological investigations in patients with Leber's optic neuropathy. van Gemert GW, Versteeg J. Doc Ophthalmol; 1989 Jan 20; 71(1):88-92. PubMed ID: 2743860 [No Abstract] [Full Text] [Related]
40. [Hyperintense optic nerve lesion on T2-weighted MRI imaging in the acute stage of Leber's hereditary optic neuropathy: a case report]. Honda H, Tsujihata M, Ochi M, Satoh A, Tomita I, Fujikawa A. Rinsho Shinkeigaku; 2006 Apr 20; 46(4):294-6. PubMed ID: 16768101 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]