These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

123 related items for PubMed ID: 20565249

  • 1. 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; 31(3):126-8. PubMed ID: 20565249
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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]

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

  • 5. [Diagnostic and differential diagnostic potential of mitochondrial DNA assessment in patients with Leber's hereditary optic neuropathy].
    Feng X, Pu W, Gao D.
    Zhonghua Yan Ke Za Zhi; 2001 May; 37(3):174-7. PubMed ID: 11864415
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. [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]

  • 8. 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 Feb; 47(11):594-604. PubMed ID: 12436196
    [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 20; 138(18):565-8. PubMed ID: 10596473
    [Abstract] [Full Text] [Related]

  • 10. Leber's hereditary optic neuropathy mutations in ethambutol-induced optic neuropathy.
    Hwang JM, Kim J, Park SS.
    J Neurol; 2003 Jan 20; 250(1):87-9. PubMed ID: 12527998
    [Abstract] [Full Text] [Related]

  • 11. 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 20; 37(8):1028-33. PubMed ID: 17045122
    [Abstract] [Full Text] [Related]

  • 12. [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 20; 41(3):243-5. PubMed ID: 15840367
    [Abstract] [Full Text] [Related]

  • 13. 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 20; 100():169-78; discussion 178-9. PubMed ID: 12545691
    [Abstract] [Full Text] [Related]

  • 14. Spectrum of the mitochondrial DNA mutations of Leber's hereditary optic neuropathy in Koreans.
    Kim JY, Hwang JM, Chang BL, Park SS.
    J Neurol; 2003 Mar 20; 250(3):278-81. PubMed ID: 12638016
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. [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 06; 47(12):1080-3. PubMed ID: 22336116
    [Abstract] [Full Text] [Related]

  • 17. [Sudden blindness: consider Leber's hereditary optic neuropathy].
    Schieving JH, de Vries BB, Hol F, Stroink H.
    Ned Tijdschr Geneeskd; 2008 Oct 25; 152(43):2313-6. PubMed ID: 19024058
    [Abstract] [Full Text] [Related]

  • 18. [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 25; 157(5):537-41. PubMed ID: 11438773
    [Abstract] [Full Text] [Related]

  • 19. [Evaluation of serum levels of SOD and MDA in patients with Leber's hereditary optic neuropathy carrying the mitochondrial DNA G11778A mutation].
    Liu Z, Sun CB, Tong Y, Qu J.
    Zhonghua Yan Ke Za Zhi; 2009 Aug 25; 45(8):719-23. PubMed ID: 20021885
    [Abstract] [Full Text] [Related]

  • 20. The epidemiology and mutation types of Leber's hereditary optic neuropathy in Thailand.
    Sathianvichitr K, Sigkaman B, Chirapapaisan N, Laowanapiban P, Padungkiatsagul T, Apinyawasisuk S, Witthayaweerasak J, Chuenkongkaew W.
    Ann Med; 2022 Dec 25; 54(1):1601-1607. PubMed ID: 35723074
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.