207 related articles for article (PubMed ID: 8728098)
1. 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]
2. [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]
3. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis.
Kellar-Wood H; Robertson N; Govan GG; Compston DA; Harding AE
Ann Neurol; 1994 Jul; 36(1):109-12. PubMed ID: 8024249
[TBL] [Abstract][Full Text] [Related]
4. 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]
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. 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]
7. Mitochondrial DNA analysis of Leber's hereditary optic neuropathy.
Hiida Y; Mashima Y; Oguchi Y; Uemura Y; Kudoh J; Sakai K; Shimizu N
Jpn J Ophthalmol; 1991; 35(1):102-6. PubMed ID: 1895564
[TBL] [Abstract][Full Text] [Related]
8. Genetic analysis of Japanese pedigrees with Leber's hereditary optic neuropathy.
Nakamura M
Kobe J Med Sci; 1993 Dec; 39(5-6):171-82. PubMed ID: 8182918
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [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]
11. [Analysis on the effect of secondary mutations on Leber's hereditary optic neuropathy].
Wang Y; Tong Y; Hu SX; Wang JY; Shao JB; Zhang HX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):397-400. PubMed ID: 17680528
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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; 38(2):163-9. PubMed ID: 7654063
[TBL] [Abstract][Full Text] [Related]
14. Homoplasmic and exclusive ND4 gene mutation in Japanese pedigrees with Leber's disease.
Nakamura M; Fujiwara Y; Yamamoto M
Invest Ophthalmol Vis Sci; 1993 Mar; 34(3):488-95. PubMed ID: 8449667
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [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]
17. High frequency of mitochondrial ND4 gene mutation in Japanese pedigrees with Leber hereditary optic neuropathy.
Nakamura M; Ara F; Yamada M; Hotta Y; Hayakawa M; Fujiki K; Kanai A; Sakai J; Inoue M; Yamamoto M
Jpn J Ophthalmol; 1992; 36(1):56-61. PubMed ID: 1635296
[TBL] [Abstract][Full Text] [Related]
18. [A molecular genetic study of Leber's disease].
Zhang LS
Zhonghua Yan Ke Za Zhi; 1993 Mar; 29(2):103-4. PubMed ID: 8404350
[TBL] [Abstract][Full Text] [Related]
19. Mutation analysis of the ND6 gene in patients with Lebers hereditary optic neuropathy.
Wissinger B; Besch D; Baumann B; Fauser S; Christ-Adler M; Jurklies B; Zrenner E; Leo-Kottler B
Biochem Biophys Res Commun; 1997 May; 234(2):511-5. PubMed ID: 9177303
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]
