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569 related items for PubMed ID: 15003728

  • 21. [Detection of mtDNA 11778 (G-->A) point mutation in a family with Leber's hereditary optic neuropathy by site-specific polymerase chain reaction].
    Niu SL, Zhang Y, Xu YF, Bu DF, Ren ZQ, Wang SY, Liu GH, Qi Y.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2003 Apr; 25(2):153-5. PubMed ID: 12905709
    [Abstract] [Full Text] [Related]

  • 22. 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
    [Abstract] [Full Text] [Related]

  • 23. [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 Jan; 59(10):777-9. PubMed ID: 12632910
    [Abstract] [Full Text] [Related]

  • 24. [Penetrance of Leber hereditary optic neuropathy in Chinese individuals with mitochondrial DNA 11778 mutation].
    Zhang Q, Guo X, Jia X, Xiao X, Guo L, Li S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Dec; 18(6):441-3. PubMed ID: 11774211
    [Abstract] [Full Text] [Related]

  • 25. Reduced frequency of known mutations in a cohort of LHON patients from India.
    Sundaresan P, Kumar SM, Thompson S, Fingert JH.
    Ophthalmic Genet; 2010 Dec; 31(4):196-9. PubMed ID: 20809775
    [Abstract] [Full Text] [Related]

  • 26. [Past, present, and future in Leber's hereditary optic neuropathy].
    Oguchi Y.
    Nippon Ganka Gakkai Zasshi; 2001 Dec; 105(12):809-27. PubMed ID: 11802455
    [Abstract] [Full Text] [Related]

  • 27. A real-time ARMS PCR/high-resolution melt curve assay for the detection of the three primary mitochondrial mutations in Leber's hereditary optic neuropathy.
    Ryan SE, Ryan F, O'Dwyer V, Neylan D.
    Mol Vis; 2016 Dec; 22():1169-1175. PubMed ID: 27746671
    [Abstract] [Full Text] [Related]

  • 28. Quantitation of heteroplasmy of mitochondrial tRNA(Leu(UUR)) gene using PCR-SSCP.
    Tanno Y, Yoneda M, Tanaka K, Tanaka H, Yamazaki M, Nishizawa M, Wakabayashi K, Ohama E, Tsuji S.
    Muscle Nerve; 1995 Dec; 18(12):1390-7. PubMed ID: 7477061
    [Abstract] [Full Text] [Related]

  • 29. 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
    [Abstract] [Full Text] [Related]

  • 30. White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation.
    Lev D, Yanoov-Sharav M, Watemberg N, Leshinsky-Silver E, Lerman-Sagie T.
    Eur J Paediatr Neurol; 2002 Mar; 6(2):121-3. PubMed ID: 11995959
    [Abstract] [Full Text] [Related]

  • 31. 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
    [Abstract] [Full Text] [Related]

  • 32. Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy.
    Tharaphan P, Chuenkongkaew WL, Luangtrakool K, Sanpachudayan T, Suktitipat B, Suphavilai R, Srisawat C, Sura T, Lertrit P.
    J Neuroophthalmol; 2006 Dec; 26(4):264-7. PubMed ID: 17204919
    [Abstract] [Full Text] [Related]

  • 33. Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy.
    Liang M, Jiang P, Li F, Zhang J, Ji Y, He Y, Xu M, Zhu J, Meng X, Zhao F, Tong Y, Liu X, Sun Y, Zhou X, Mo JQ, Qu J, Guan MX.
    Invest Ophthalmol Vis Sci; 2014 Mar 06; 55(3):1321-31. PubMed ID: 24398099
    [Abstract] [Full Text] [Related]

  • 34. 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 Mar 06; 100():169-78; discussion 178-9. PubMed ID: 12545691
    [Abstract] [Full Text] [Related]

  • 35. Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family.
    Kaplanová V, Zeman J, Hansíková H, Cerná L, Houst'ková H, Misovicová N, Houstek J.
    J Neurol Sci; 2004 Aug 30; 223(2):149-55. PubMed ID: 15337616
    [Abstract] [Full Text] [Related]

  • 36. Leber's hereditary optic neuropathy: a multifactorial disease.
    Yen MY, Wang AG, Wei YH.
    Prog Retin Eye Res; 2006 Jul 30; 25(4):381-96. PubMed ID: 16829155
    [Abstract] [Full Text] [Related]

  • 37. 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 30; 11(2):115-8. PubMed ID: 17254817
    [Abstract] [Full Text] [Related]

  • 38. 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 30; 34(3):488-95. PubMed ID: 8449667
    [Abstract] [Full Text] [Related]

  • 39. [Mutation analysis in a family of Leber hereditary optic neuropathy].
    She CY, Gu H, Xu J, Ma K, Liu NP.
    Zhonghua Yan Ke Za Zhi; 2011 Dec 30; 47(12):1080-3. PubMed ID: 22336116
    [Abstract] [Full Text] [Related]

  • 40. [DNA diagnosis in the age of individual made-to-order medications].
    Mashima Y.
    Nippon Ganka Gakkai Zasshi; 2004 Dec 30; 108(12):863-85; discussion 886. PubMed ID: 15656090
    [Abstract] [Full Text] [Related]

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