606 related articles for article (PubMed ID: 11864415)
1. [Diagnostic and differential diagnostic potential of mitochondrial DNA assessment in patients with Leber's hereditary optic neuropathy].
Feng X; Pu W; Gao D
Zhonghua Yan Ke Za Zhi; 2001 May; 37(3):174-7. PubMed ID: 11864415
[TBL] [Abstract][Full Text] [Related]
2. Diagnostic potential of mitochondrial DNA assessment in patients with optic neuropathy.
Feng X; Pu W; Gao D; Isashiki Y; Ohba N
Chin Med J (Engl); 2000 Aug; 113(8):743-6. PubMed ID: 11776061
[TBL] [Abstract][Full Text] [Related]
3. Leber's hereditary optic neuropathy mutations in ethambutol-induced optic neuropathy.
Hwang JM; Kim J; Park SS
J Neurol; 2003 Jan; 250(1):87-9. PubMed ID: 12527998
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
Pénisson-Besnier I; Moreau C; Jacques C; Roger JC; Dubas F; Reynier P
Rev Neurol (Paris); 2001 May; 157(5):537-41. PubMed ID: 11438773
[TBL] [Abstract][Full Text] [Related]
6. Nonfamilial and unusual cases of Leber's hereditary optic neuropathy identified by mitochondrial DNA analysis.
Isashiki Y; Ohba N; Uto M; Nakagawa M; Nakano T; Kitahara K; Hotta A; Okamura R; Ozaki M; Futami Y
Jpn J Ophthalmol; 1992; 36(2):197-204. PubMed ID: 1513067
[TBL] [Abstract][Full Text] [Related]
7. Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.
Leo-Kottler B; Christ-Adler M; Baumann B; Zrenner E; Wissinger B
Ger J Ophthalmol; 1996 Jul; 5(4):233-40. PubMed ID: 8854108
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. [Sudden blindness: consider Leber's hereditary optic neuropathy].
Schieving JH; de Vries BB; Hol F; Stroink H
Ned Tijdschr Geneeskd; 2008 Oct; 152(43):2313-6. PubMed ID: 19024058
[TBL] [Abstract][Full Text] [Related]
10. Rapid quantification of the heteroplasmy of mutant mitochondrial DNAs in Leber's hereditary optic neuropathy using the Invader technology.
Mashima Y; Nagano M; Funayama T; Zhang Q; Egashira T; Kudho J; Shimizu N; Oguchi Y
Clin Biochem; 2004 Apr; 37(4):268-76. PubMed ID: 15003728
[TBL] [Abstract][Full Text] [Related]
11. [Rapid genetic screening of Leber's hereditary optic neuropathy with mtDNA G11778A mutation by AS-PCR with whole blood].
Yang JH; Tong Y; Li BH; Chen YK
Zhonghua Yan Ke Za Zhi; 2005 Mar; 41(3):243-5. PubMed ID: 15840367
[TBL] [Abstract][Full Text] [Related]
12. Lack of association between Leber's hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran.
Houshmand M; Sanati MH; Rashedi I; Sharifpanah F; Asghari E; Lotfi J
Eur Neurol; 2004; 51(2):68-71. PubMed ID: 14671420
[TBL] [Abstract][Full Text] [Related]
13. Case report: A Thai patient with Leber's hereditary optic neuropathy linked to mitochondrial DNA 14484 mutation.
Chuenkongkaew W; Lertrit P; Suphavilai R
Southeast Asian J Trop Med Public Health; 2004 Mar; 35(1):167-8. PubMed ID: 15272763
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. Leber's hereditary optic neuropathy with childhood onset.
Barboni P; Savini G; Valentino ML; La Morgia C; Bellusci C; De Negri AM; Sadun F; Carta A; Carbonelli M; Sadun AA; Carelli V
Invest Ophthalmol Vis Sci; 2006 Dec; 47(12):5303-9. PubMed ID: 17122117
[TBL] [Abstract][Full Text] [Related]
18. Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation--A case report.
Grazina MM; Diogo LM; Garcia PC; Silva ED; Garcia TD; Robalo CB; Oliveira CR
Eur J Paediatr Neurol; 2007 Mar; 11(2):115-8. PubMed ID: 17254817
[TBL] [Abstract][Full Text] [Related]
19. Leber's hereditary optic neuropathy: clinical and molecular profile of a Brazilian sample.
Maciel-Guerra AT; Zanchetta LM; Amaral Fernandes MS; Andrade PB; do Amor Divino Miranda PM; Sartorato EL
Ophthalmic Genet; 2010 Sep; 31(3):126-8. PubMed ID: 20565249
[TBL] [Abstract][Full Text] [Related]
20. [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
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
