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Journal Abstract Search

159 related items for PubMed ID: 16523671

  • 1. [Spectrum of pathogenic mtDNA mutations in Leber hereditary optic neuropathy families from Siberia].
    Volod'ko NV, L'vova MA, Starikovskaia EB, Derbeneva OA, Bychkov IIu, Mikhaĭlovskaia IE, Pogozheva IV, Fedotov FF, Soyan GV, Procaccio V, Wallace DC, Sukernik RI.
    Genetika; 2006 Jan; 42(1):89-97. PubMed ID: 16523671
    [Abstract] [Full Text] [Related]

  • 2. [The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].
    Mao YJ, Qu J, Guan MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb; 25(1):45-9. PubMed ID: 18247303
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Mitochondrial D-loop variation in leber hereditary neuropathy patients harboring primary G11778A, G3460A, T14484C mutations: J and W haplogroups as high-risk factors.
    Shafa Shariat Panahi M, Houshmand M, Tabassi AR.
    Arch Med Res; 2006 Nov; 37(8):1028-33. PubMed ID: 17045122
    [Abstract] [Full Text] [Related]

  • 5. Leber's hereditary optic neuroretinopathy (LHON) associated with mitochondrial DNA point mutation G11778A in two Croatian families.
    Martin-Kleiner I, Gabrilovac J, Bradvica M, Vidović T, Cerovski B, Fumić K, Boranić M.
    Coll Antropol; 2006 Mar; 30(1):171-4. PubMed ID: 16617593
    [Abstract] [Full Text] [Related]

  • 6. Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.
    Sudoyo H, Suryadi H, Lertrit P, Pramoonjago P, Lyrawati D, Marzuki S.
    J Hum Genet; 2002 Mar; 47(11):594-604. PubMed ID: 12436196
    [Abstract] [Full Text] [Related]

  • 7. [Penetrance of Leber hereditary optic neuropathy individuals with mitochondrial DNA 11778 mutation in the Shanxi area].
    Zheng ML, Zhang GL, Hua AL, Zhang YL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr; 21(2):166-7. PubMed ID: 15079802
    [Abstract] [Full Text] [Related]

  • 8. Mitochondrial abnormalities in patients with LHON-like optic neuropathies.
    Abu-Amero KK, Bosley TM.
    Invest Ophthalmol Vis Sci; 2006 Oct; 47(10):4211-20. PubMed ID: 17003408
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. Haplogroup heterogeneity of LHON patients carrying the m.14484T>C mutation in India.
    Khan NA, Govindaraj P, Soumittra N, Srilekha S, Ambika S, Vanniarajan A, Meena AK, Uppin MS, Sundaram C, Taly AB, Bindu PS, Gayathri N, Thangaraj K.
    Invest Ophthalmol Vis Sci; 2013 Jun 10; 54(6):3999-4005. PubMed ID: 23674761
    [Abstract] [Full Text] [Related]

  • 11. A patient with two mitochondrial DNA mutations causing PEO and LHON.
    Melberg A, Moslemi AR, Palm O, Raininko R, Stålberg E, Oldfors A.
    Eur J Med Genet; 2009 Jun 10; 52(1):47-8. PubMed ID: 19015050
    [Abstract] [Full Text] [Related]

  • 12. [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 10; 47(12):1080-3. PubMed ID: 22336116
    [Abstract] [Full Text] [Related]

  • 13. Leber's hereditary optic neuropathy is associated with the mitochondrial ND6 T14484C mutation in three Chinese families.
    Sun YH, Wei QP, Zhou X, Qian Y, Zhou J, Lu F, Qu J, Guan MX.
    Biochem Biophys Res Commun; 2006 Aug 18; 347(1):221-5. PubMed ID: 16806060
    [Abstract] [Full Text] [Related]

  • 14. 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 18; 31(3):126-8. PubMed ID: 20565249
    [Abstract] [Full Text] [Related]

  • 15. [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 Sep 18; 59(10):777-9. PubMed ID: 12632910
    [Abstract] [Full Text] [Related]

  • 16. Mitochondrial DNA mutation m.3635G>A may be associated with Leber hereditary optic neuropathy in Chinese.
    Zhang AM, Zou Y, Guo X, Jia X, Zhang Q, Yao YG.
    Biochem Biophys Res Commun; 2009 Aug 21; 386(2):392-5. PubMed ID: 19527690
    [Abstract] [Full Text] [Related]

  • 17. [Detection of mtDNA*LHON G11778A mutation by real-time polymerase chain reaction using TaqMan-MGB probe technology].
    Li YM, Wang JY, Chen Y, Shao JB, Wang J, Tong Y.
    Zhonghua Yan Ke Za Zhi; 2006 Aug 21; 42(8):728-32. PubMed ID: 17081446
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 39(1):8-18. PubMed ID: 9027481
    [Abstract] [Full Text] [Related]

  • 19. Leber's hereditary optic neuropathy: the spectrum of mitochondrial DNA mutations in Iranian patients.
    Houshmand M, Sharifpanah F, Tabasi A, Sanati MH, Vakilian M, Lavasani SH, Joughehdoust S.
    Ann N Y Acad Sci; 2004 Apr 01; 1011():345-9. PubMed ID: 15126312
    [Abstract] [Full Text] [Related]

  • 20. Influence of mutation type on clinical expression of Leber hereditary optic neuropathy.
    Spruijt L, Kolbach DN, de Coo RF, Plomp AS, Bauer NJ, Smeets HJ, de Die-Smulders CE.
    Am J Ophthalmol; 2006 Apr 01; 141(4):676-82. PubMed ID: 16564802
    [Abstract] [Full Text] [Related]

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