82 related articles for article (PubMed ID: 11195136)
1. False positive molecular diagnosis of Leber's hereditary optic neuropathy.
Yen MY; Wang AG; Chang WL; Hsu WM; Liu JH; Wei YH
Zhonghua Yi Xue Za Zhi (Taipei); 2000 Dec; 63(12):864-8. PubMed ID: 11195136
[TBL] [Abstract][Full Text] [Related]
2. Molecular diagnosis of Leber's hereditary optic neuropathy.
Yen MY; Liu JH; Pang CY; Wei YH
J Formos Med Assoc; 1993 Jan; 92(1):42-5. PubMed ID: 8099825
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Risk of false-positive molecular genetic diagnosis of Leber's hereditary optic neuropathy.
Mashima Y; Hiida Y; Saga M; Oguchi Y; Kudoh J; Shimizu N
Am J Ophthalmol; 1995 Feb; 119(2):245-6. PubMed ID: 7832241
[TBL] [Abstract][Full Text] [Related]
5. Leber's hereditary optic neuropathy mitochondrial DNA mutations in familial multiple sclerosis.
Mojon DS; Fujihara K; Hirano M; Miller C; Lincoff NS; Jacobs LD; Greenberg SJ
Graefes Arch Clin Exp Ophthalmol; 1999 Apr; 237(4):348-50. PubMed ID: 10208269
[TBL] [Abstract][Full Text] [Related]
6. Leber's hereditary optic neuropathy mitochondrial DNA mutations at nucleotides 11778 and 3460 in multiple sclerosis.
Mojon DS; Herbert J; Sadiq SA; Miller JR; Madonna M; Hirano M
Ophthalmologica; 1999; 213(3):171-5. PubMed ID: 10202290
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. 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]
9. [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; 138(18):565-8. PubMed ID: 10596473
[TBL] [Abstract][Full Text] [Related]
10. Quantitative determination of heteroplasmy in Leber's hereditary optic neuropathy by single-strand conformation polymorphism.
Mashima Y; Saga M; Hiida Y; Oguchi Y; Wakakura M; Kudoh J; Shimizu N
Invest Ophthalmol Vis Sci; 1995 Jul; 36(8):1714-20. PubMed ID: 7601652
[TBL] [Abstract][Full Text] [Related]
11. Exclusive homoplasmic 11778 mutation in mitochondrial DNA of Chinese patients with Leber's hereditary optic neuropathy.
Yen MY; Lee HC; Wang AG; Chang WL; Liu JH; Wei YH
Jpn J Ophthalmol; 1999; 43(3):196-200. PubMed ID: 10413253
[TBL] [Abstract][Full Text] [Related]
12. Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population.
Dogulu CF; Kansu T; Seyrantepe V; Ozguc M; Topaloglu H; Johns DR
Eye (Lond); 2001 Apr; 15(Pt 2):183-8. PubMed ID: 11339587
[TBL] [Abstract][Full Text] [Related]
13. Mae III positively detects the mitochondrial mutation associated with type I Leber's hereditary optic neuropathy.
Stone EM; Coppinger JM; Kardon RH; Donelson J
Arch Ophthalmol; 1990 Oct; 108(10):1417-20. PubMed ID: 1977373
[TBL] [Abstract][Full Text] [Related]
14. Pitfalls in the molecular genetic diagnosis of Leber hereditary optic neuropathy (LHON).
Johns DR; Neufeld MJ
Am J Hum Genet; 1993 Oct; 53(4):916-20. PubMed ID: 8213820
[TBL] [Abstract][Full Text] [Related]
15. [Analysis of mutations and heteroplasmy at mitochondrial DNA 11778 using non-RI single strand conformation polymorphisms in Leber's hereditary optic neuropathy].
Toyo-Oka Y; Wada C; Yamabe H; Inoue M; Ishigaki M; Matsuyama N; Ohnuki Y; Ichibe Y; Wakakura M; Ohtani H
Rinsho Byori; 1996 Jul; 44(7):676-80. PubMed ID: 8741498
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [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]
18. [Mitochondrial DNA mutation in Leber's hereditary optic neuropathy in China].
Zhang LS; Huang Y; Li FY
Zhonghua Yi Xue Za Zhi; 1994 Jun; 74(6):349-51, 390. PubMed ID: 7994643
[TBL] [Abstract][Full Text] [Related]
19. A mutation of mitochondrial DNA in Japanese families with Leber's hereditary optic neuropathy.
Fujiki K; Hotta Y; Hayakawa M; Saito K; Ara F; Ueda S; Goto T; Ishida M; Yanashima K; Shiono T
Jinrui Idengaku Zasshi; 1991 Jun; 36(2):143-7. PubMed ID: 1681125
[TBL] [Abstract][Full Text] [Related]
20. Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation.
Murakami T; Mita S; Tokunaga M; Maeda H; Ueyama H; Kumamoto T; Uchino M; Ando M
J Neurol Sci; 1996 Oct; 142(1-2):111-3. PubMed ID: 8902729
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
