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Journal Abstract Search

160 related items for PubMed ID: 8401538

  • 1. Screening for the two most frequent mutations in Leber's hereditary optic neuropathy by duplex PCR based on allele-specific amplification.
    Nørby S.
    Hum Mutat; 1993; 2(4):309-13. PubMed ID: 8401538
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. [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
    [Abstract] [Full Text] [Related]

  • 4. Mutation detection in Leber's hereditary optic neuropathy by PCR with allele-specific priming.
    Nørby S, Lestienne P, Nelson I, Rosenberg T.
    Biochem Biophys Res Commun; 1991 Mar 15; 175(2):631-6. PubMed ID: 2018507
    [Abstract] [Full Text] [Related]

  • 5. [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 15; 44(7):676-80. PubMed ID: 8741498
    [Abstract] [Full Text] [Related]

  • 6. [Molecular genetic analysis for Leber's hereditary optic neuropathy (LHON)].
    Tanno Y, Yoneda M, Tanaka K, Tsuji S.
    Nihon Rinsho; 1993 Sep 15; 51(9):2396-402. PubMed ID: 8411719
    [Abstract] [Full Text] [Related]

  • 7. [Leber's optic neuropathy: new diagnostic prospects].
    Pagot V, Malecaze F, Rötig A, Simorre V, Maillard P, Mathis A, Munnich A.
    J Fr Ophtalmol; 1992 Sep 15; 15(1):19-23. PubMed ID: 1602101
    [Abstract] [Full Text] [Related]

  • 8. A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies.
    Seibel P, Flierl A, Kottlors M, Reichmann H.
    Biochem Biophys Res Commun; 1994 Apr 29; 200(2):938-42. PubMed ID: 8179630
    [Abstract] [Full Text] [Related]

  • 9. [A molecular genetic study of Leber's disease].
    Zhang LS.
    Zhonghua Yan Ke Za Zhi; 1993 Mar 29; 29(2):103-4. PubMed ID: 8404350
    [Abstract] [Full Text] [Related]

  • 10. [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 29; 41(3):243-5. PubMed ID: 15840367
    [Abstract] [Full Text] [Related]

  • 11. 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 29; 38(4):693-700. PubMed ID: 8728098
    [Abstract] [Full Text] [Related]

  • 12. Clinical correlation of mitochondrial DNA heteroplasmy and Leber's hereditary optic neuropathy.
    Isashiki Y, Nakagawa M.
    Jpn J Ophthalmol; 1991 Apr 29; 35(3):259-67. PubMed ID: 1770665
    [Abstract] [Full Text] [Related]

  • 13. [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 Apr 29; 20(1):65-70. PubMed ID: 9099286
    [Abstract] [Full Text] [Related]

  • 14. [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 29; 24(4):397-400. PubMed ID: 17680528
    [Abstract] [Full Text] [Related]

  • 15. 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 29; 5(4):233-40. PubMed ID: 8854108
    [Abstract] [Full Text] [Related]

  • 16. Fast capillary electrophoresis-laser induced fluorescence analysis of ligase chain reaction products: human mitochondrial DNA point mutations causing Leber's hereditary optic neuropathy.
    Muth J, Williams PM, Williams SJ, Brown MD, Wallace DC, Karger BL.
    Electrophoresis; 1996 Dec 29; 17(12):1875-83. PubMed ID: 9034769
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. 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 29; 37(4):268-76. PubMed ID: 15003728
    [Abstract] [Full Text] [Related]

  • 19. Mutation-specific PCR: a rapid and inexpensive diagnostic method, as exemplified by mitochondrial DNA analysis in Leber's hereditary optic neuropathy.
    Nørby S.
    DNA Cell Biol; 1993 Apr 29; 12(6):549-52. PubMed ID: 8101084
    [Abstract] [Full Text] [Related]

  • 20. A new mitochondrial DNA mutation in the tRNA leucine 1 gene (C3275A) in a patient with Leber's hereditary optic neuropathy.
    Garcia-Lozano JR, Aguilera I, Bautista J, Nuñez-Roldan A.
    Hum Mutat; 2000 Jan 29; 15(1):120-1. PubMed ID: 10612844
    [No Abstract] [Full Text] [Related]

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