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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 15804271)

  • 1. An unusual family with Leber's hereditary optic neuropathy and facioscapulohumeral muscular dystrophy.
    Chuenkongkaew WL; Lertrit P; Limwongse C; Nilanont Y; Boonyapisit K; Sangruchi T; Chirapapaisan N; Suphavilai R
    Eur J Neurol; 2005 May; 12(5):388-91. PubMed ID: 15804271
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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; 47(12):1080-3. PubMed ID: 22336116
    [TBL] [Abstract][Full Text] [Related]  

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

  • 4. [A pedigree of Leber's hereditary optic neuropathy with mtDNA 14484 mutation].
    Tong Y; Wang Y; Jiang F; Liu B; Zhang S; Yang W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):531-3. PubMed ID: 18841565
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 55(3):1321-31. PubMed ID: 24398099
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 100():169-78; discussion 178-9. PubMed ID: 12545691
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy.
    Osborne RJ; Welle S; Venance SL; Thornton CA; Tawil R
    Neurology; 2007 Feb; 68(8):569-77. PubMed ID: 17151338
    [TBL] [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; 41(3):243-5. PubMed ID: 15840367
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondrial dysfunction due to Leber's hereditary optic neuropathy as a cause of visual loss during assessment for epilepsy surgery.
    Niehusmann P; Surges R; von Wrede RD; Elger CE; Wellmer J; Reimann J; Urbach H; Vielhaber S; Bien CG; Kunz WS
    Epilepsy Behav; 2011 Jan; 20(1):38-43. PubMed ID: 21145289
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation.
    Cai W; Fu Q; Zhou X; Qu J; Tong Y; Guan MX
    J Genet Genomics; 2008 Nov; 35(11):649-55. PubMed ID: 19022198
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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; 45(8):719-23. PubMed ID: 20021885
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phylogenetic assessment of the mitochondrial DNA displacement loop haplotype in Japanese patients with Leber's hereditary optic neuropathy harboring the mitochondrial DNA G11778A mutation.
    Isashiki Y; Sonoda S; Izumo S; Sakamoto T; Tachikui H; Inoue I
    Ophthalmic Res; 2003; 35(4):224-31. PubMed ID: 12815198
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis.
    Kim JY; Hwang JM; Park SS
    Ann Neurol; 2002 May; 51(5):630-4. PubMed ID: 12112111
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. m.3635G>A mutation as a cause of Leber hereditary optic neuropathy.
    Kodroń A; Krawczyński MR; Tońska K; Bartnik E
    J Clin Pathol; 2014 Jul; 67(7):639-41. PubMed ID: 24747208
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.