262 related articles for article (PubMed ID: 7804415)
21. Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA.
Hotta Y; Fujiki K; Hayakawa M; Nakajima A; Kanai A; Mashima Y; Hiida Y; Shinoda K; Yamada K; Oguchi Y
Jpn J Ophthalmol; 1995; 39(1):96-108. PubMed ID: 7643491
[TBL] [Abstract][Full Text] [Related]
22. Characterization of the mitochondrial genome in childhood multiple sclerosis. II. Multiple sclerosis without optic neuritis and LHON-associated genes.
Wilichowski E; Ohlenbusch A; Hanefeld F
Neuropediatrics; 1998 Dec; 29(6):307-12. PubMed ID: 10029350
[TBL] [Abstract][Full Text] [Related]
23. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes.
Hofmann S; Bezold R; Jaksch M; Obermaier-Kusser B; Mertens S; Kaufhold P; Rabl W; Hecker W; Gerbitz KD
Genomics; 1997 Jan; 39(1):8-18. PubMed ID: 9027481
[TBL] [Abstract][Full Text] [Related]
24. Spectrum of the mitochondrial DNA mutations of Leber's hereditary optic neuropathy in Koreans.
Kim JY; Hwang JM; Chang BL; Park SS
J Neurol; 2003 Mar; 250(3):278-81. PubMed ID: 12638016
[TBL] [Abstract][Full Text] [Related]
25. Mitochondrial DNA mutation in Leber's hereditary optic neuropathy.
Yen MY; Yen TC; Pang CY; Liu JH; Wei YH
Invest Ophthalmol Vis Sci; 1992 Jul; 33(8):2561-6. PubMed ID: 1634353
[TBL] [Abstract][Full Text] [Related]
26. Sporadic bilateral optic neuropathy in children: the role of mitochondrial abnormalities.
Bosley TM; Brodsky MC; Glasier CM; Abu-Amero KK
Invest Ophthalmol Vis Sci; 2008 Dec; 49(12):5250-6. PubMed ID: 18676632
[TBL] [Abstract][Full Text] [Related]
27. [Clinical examination of Leber hereditary optic neuropathy in patients with the same gene mutation].
Chelstowska J; Mroczek K; Niebudek D; Małecka-Idzikowska A; Bartnik E; Hanna Nizankowska M; Sasiadek M
Przegl Lek; 2002; 59(10):777-9. PubMed ID: 12632910
[TBL] [Abstract][Full Text] [Related]
28. [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]
29. Clinical, genetic, and biochemical characterization of a Leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations.
Brown MD; Allen JC; Van Stavern GP; Newman NJ; Wallace DC
Am J Med Genet; 2001 Dec; 104(4):331-8. PubMed ID: 11754070
[TBL] [Abstract][Full Text] [Related]
30. Clinical spectrum of Leber's hereditary optic neuropathy.
Kerrison JB; Newman NJ
Clin Neurosci; 1997; 4(5):295-301. PubMed ID: 9292259
[TBL] [Abstract][Full Text] [Related]
31. [Optic neuropathy caused by alcoholism and smoking: a diagnostic pitfall of Leber's optic neuropathy].
Borruat FX; Hirt L; Regli F
Rev Neurol (Paris); 1994 Nov; 150(11):799-801. PubMed ID: 7597375
[TBL] [Abstract][Full Text] [Related]
32. 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; 82(1):59-64. PubMed ID: 10087740
[TBL] [Abstract][Full Text] [Related]
33. [Molecular genetic analysis for Leber's hereditary optic neuropathy (LHON)].
Tanno Y; Yoneda M; Tanaka K; Tsuji S
Nihon Rinsho; 1993 Sep; 51(9):2396-402. PubMed ID: 8411719
[TBL] [Abstract][Full Text] [Related]
34. Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations.
Ferré M; Bonneau D; Milea D; Chevrollier A; Verny C; Dollfus H; Ayuso C; Defoort S; Vignal C; Zanlonghi X; Charlin JF; Kaplan J; Odent S; Hamel CP; Procaccio V; Reynier P; Amati-Bonneau P
Hum Mutat; 2009 Jul; 30(7):E692-705. PubMed ID: 19319978
[TBL] [Abstract][Full Text] [Related]
35. African, Native American, and European mitochondrial DNAs in Cubans from Pinar del Rio Province and implications for the recent epidemic neuropathy in Cuba. Cuba Neuropathy Field Investigation Team.
Torroni A; Brown MD; Lott MT; Newman NJ; Wallace DC
Hum Mutat; 1995; 5(4):310-7. PubMed ID: 7627185
[TBL] [Abstract][Full Text] [Related]
36. Mitochondrial abnormalities in patients with LHON-like optic neuropathies.
Abu-Amero KK; Bosley TM
Invest Ophthalmol Vis Sci; 2006 Oct; 47(10):4211-20. PubMed ID: 17003408
[TBL] [Abstract][Full Text] [Related]
37. A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy.
Sadun AA; Carelli V; Salomao SR; Berezovsky A; Quiros P; Sadun F; DeNegri AM; Andrade R; Schein S; Belfort R
Trans Am Ophthalmol Soc; 2002; 100():169-78; discussion 178-9. PubMed ID: 12545691
[TBL] [Abstract][Full Text] [Related]
38. Mitochondrial DNA mutations associated with the 11778 mutation in Leber's disease.
Sawano T; Tanaka M; Ohno K; Yoneda M; Ota Y; Terasaki H; Awaya S; Ozawa T
Biochem Mol Biol Int; 1996 Apr; 38(4):693-700. PubMed ID: 8728098
[TBL] [Abstract][Full Text] [Related]
39. [Correlation between clinical and molecular genetic findings in Leber's optic atrophy].
Leo-Kottler B; Christ-Adler M; Reck B; Wissinger B; Zrenner E
Ophthalmologe; 1995 Feb; 92(1):86-92. PubMed ID: 7719084
[TBL] [Abstract][Full Text] [Related]
40. [Positive diagnosis of Leber's hereditary optic neuropathy using molecular genetics].
Souied E; Pisella PJ; Ossareh B; Brézin A; Junes P; Wild-Decrette C; Munnich A; Bonnefont JP; Mondon H
J Fr Ophtalmol; 1997; 20(1):65-70. PubMed ID: 9099286
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]