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 *

208 related articles for article (PubMed ID: 21174521)

  • 21. 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]  

  • 22. Retinal ganglion cell analysis in Leber's hereditary optic neuropathy.
    Akiyama H; Kashima T; Li D; Shimoda Y; Mukai R; Kishi S
    Ophthalmology; 2013 Sep; 120(9):1943-4.e5. PubMed ID: 24001531
    [No 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; 59(10):777-9. PubMed ID: 12632910
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [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]  

  • 25. Posterior reversible encephalopathy syndrome in a leber hereditary optic neuropathy patient with mitochondrial DNA 11778G>A point mutation.
    Da Y; Zhang X; Li F; Yang X; Zhang X; Jia J
    J Neuroophthalmol; 2013 Sep; 33(3):276-8. PubMed ID: 23782927
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Treatment of Leber's hereditary optic neuropathy: theory to practice.
    Johns DR; Colby KA
    Semin Ophthalmol; 2002 Mar; 17(1):33-8. PubMed ID: 15513454
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Comparison of retinal nerve fibre layers between 11778 and 14484 mutations in Leber's hereditary optic neuropathy.
    Seo JH; Hwang JM; Park SS
    Eye (Lond); 2010 Jan; 24(1):107-11. PubMed ID: 19247386
    [TBL] [Abstract][Full Text] [Related]  

  • 28. LHON/MELAS overlap mutation in ND1 subunit of mitochondrial complex I affects ubiquinone binding as revealed by modeling in Escherichia coli NDH-1.
    Pätsi J; Maliniemi P; Pakanen S; Hinttala R; Uusimaa J; Majamaa K; Nyström T; Kervinen M; Hassinen IE
    Biochim Biophys Acta; 2012 Feb; 1817(2):312-8. PubMed ID: 22079202
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. [Leber's hereditary optic neuropathy (LHON) with mutation at G3460A and MS-like phenotype].
    Jamrozik Z; Tutaj A; Piechowski-Jóźwiak B; Mroczek-Tońska K; Bartnik E; Kwieciński H
    Neurol Neurochir Pol; 2003; 37(3):713-20. PubMed ID: 14593764
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [MELAS syndrome masquerading as herpes encephalitis: genetic diagnosis].
    de Toledo M; Díaz-Guzmán J; Pérez-Martínez DA; Sáiz-Díaz RA; Rodríguez-Vallejo A; Campos Y
    Rev Neurol; 2001 Jul 16-31; 33(2):148-50. PubMed ID: 11562875
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mitochondrial T9957C mutation in association with NAION and seizures but not MELAS.
    Abu-Amero KK; Bosley TM; Bohlega S; Hansen E
    Ophthalmic Genet; 2005 Mar; 26(1):31-6. PubMed ID: 15823923
    [TBL] [Abstract][Full Text] [Related]  

  • 33. MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes.
    Nakamura M; Yabe I; Sudo A; Hosoki K; Yaguchi H; Saitoh S; Sasaki H
    J Med Genet; 2010 Oct; 47(10):659-64. PubMed ID: 20610441
    [TBL] [Abstract][Full Text] [Related]  

  • 34. MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA.
    Taylor RW; Chinnery PF; Haldane F; Morris AA; Bindoff LA; Wilson J; Turnbull DM
    Ann Neurol; 1996 Sep; 40(3):459-62. PubMed ID: 8797538
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Diagnosis and management of MELAS.
    Thambisetty M; Newman NJ
    Expert Rev Mol Diagn; 2004 Sep; 4(5):631-44. PubMed ID: 15347257
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. [Leber hereditary optic neuropathy and optic neuritis: similarities and differences of clinical characteristics].
    Lai CT; Wang Q; Li Z; Wang W; Zhu J; Lu Y; Zhang XJ; Yu HF
    Zhonghua Yan Ke Za Zhi; 2007 Sep; 43(9):793-7. PubMed ID: 18070523
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [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]  

  • 40. White Matter Changes in Two Leber's Hereditary Optic Neuropathy Pedigrees: 12-Year Follow-Up.
    Jančić J; Dejanović I; Radovanović S; Ostojić J; Kozić D; Đurić-Jovičić M; Samardžić J; Ćetković M; Kostić V
    Ophthalmologica; 2016; 235(1):49-56. PubMed ID: 26540208
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.