BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

434 related articles for article (PubMed ID: 30128709)

  • 1. Mitochondrial DNA mutations in late-onset Leigh syndrome.
    Wei Y; Cui L; Peng B
    J Neurol; 2018 Oct; 265(10):2388-2395. PubMed ID: 30128709
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Clinical and genetic characteristics of children with Leigh syndrome].
    Fang F; Shen Y; Shen DM; Liu ZM; Ding CH; Zhang WC; Sun SZ; Lyu JL; Han TL; Wang XH; Zhang WH; Yang XY; Li JW; Wu HS
    Zhonghua Er Ke Za Zhi; 2017 Mar; 55(3):205-209. PubMed ID: 28273704
    [No Abstract]   [Full Text] [Related]  

  • 3. Clinical, Neuroimaging, and Pathological Analyses of 13 Chinese Leigh Syndrome Patients with Mitochondrial DNA Mutations.
    Yu XL; Yan CZ; Ji KQ; Lin PF; Xu XB; Dai TJ; Li W; Zhao YY
    Chin Med J (Engl); 2018 Nov; 131(22):2705-2712. PubMed ID: 30425197
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Multisystem mitochondrial diseases due to mutations in mtDNA-encoded subunits of complex I.
    Danhelovska T; Kolarova H; Zeman J; Hansikova H; Vaneckova M; Lambert L; Kucerova-Vidrova V; Berankova K; Honzik T; Tesarova M
    BMC Pediatr; 2020 Jan; 20(1):41. PubMed ID: 31996177
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cytochrome C oxydase deficiency: SURF1 gene investigation in patients with Leigh syndrome.
    Maalej M; Kammoun T; Alila-Fersi O; Kharrat M; Ammar M; Felhi R; Mkaouar-Rebai E; Keskes L; Hachicha M; Fakhfakh F
    Biochem Biophys Res Commun; 2018 Mar; 497(4):1043-1048. PubMed ID: 29481804
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genotype-phenotype analysis of MT-ATP6-associated Leigh syndrome.
    Na JH; Lee YM
    Acta Neurol Scand; 2022 Apr; 145(4):414-422. PubMed ID: 34877647
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutations.
    Sonam K; Khan NA; Bindu PS; Taly AB; Gayathri N; Bharath MM; Govindaraju C; Arvinda HR; Nagappa M; Sinha S; Thangaraj K
    Brain Dev; 2014 Oct; 36(9):807-12. PubMed ID: 24262866
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical and molecular survey in 124 Chinese patients with Leigh or Leigh-like syndrome.
    Zhang Y; Yang YL; Sun F; Cai X; Qian N; Yuan Y; Wang ZX; Qi Y; Xiao JX; Wang XY; Zhang YH; Jiang YW; Qin J; Wu XR
    J Inherit Metab Dis; 2007 Apr; 30(2):265. PubMed ID: 17323145
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The mitochondrial DNA 10197 G > A mutation causes MELAS/Leigh overlap syndrome presenting with acute auditory agnosia.
    Leng Y; Liu Y; Fang X; Li Y; Yu L; Yuan Y; Wang Z
    Mitochondrial DNA; 2015 Apr; 26(2):208-12. PubMed ID: 24708134
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Late-onset Leigh syndrome with myoclonic epilepsy with ragged-red fibers.
    Monden Y; Mori M; Kuwajima M; Goto T; Yamagata T; Momoi MY
    Brain Dev; 2013 Jun; 35(6):582-5. PubMed ID: 22981260
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [3-Hydroxy-isobutyryl-CoA hydrolase deficiency in a child with Leigh-like syndrome and literature review].
    Zhu H; Bao X; Zhang Y
    Zhonghua Er Ke Za Zhi; 2015 Aug; 53(8):626-30. PubMed ID: 26717663
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mortality of Japanese patients with Leigh syndrome: Effects of age at onset and genetic diagnosis.
    Ogawa E; Fushimi T; Ogawa-Tominaga M; Shimura M; Tajika M; Ichimoto K; Matsunaga A; Tsuruoka T; Ishige M; Fuchigami T; Yamazaki T; Kishita Y; Kohda M; Imai-Okazaki A; Okazaki Y; Morioka I; Ohtake A; Murayama K
    J Inherit Metab Dis; 2020 Jul; 43(4):819-826. PubMed ID: 31967322
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Heteroplasmic Mutant Load Differences in Mitochondrial DNA-Associated Leigh Syndrome.
    Na JH; Lee YM
    Pediatr Neurol; 2023 Jan; 138():27-32. PubMed ID: 36335839
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A guide to diagnosis and treatment of Leigh syndrome.
    Baertling F; Rodenburg RJ; Schaper J; Smeitink JA; Koopman WJ; Mayatepek E; Morava E; Distelmaier F
    J Neurol Neurosurg Psychiatry; 2014 Mar; 85(3):257-65. PubMed ID: 23772060
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Leigh syndrome: Resolving the clinical and genetic heterogeneity paves the way for treatment options.
    Gerards M; Sallevelt SC; Smeets HJ
    Mol Genet Metab; 2016 Mar; 117(3):300-12. PubMed ID: 26725255
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome.
    Yang YL; Sun F; Zhang Y; Qian N; Yuan Y; Wang ZX; Qi Y; Xiao JX; Wang XY; Qi ZY; Zhang YH; Jiang YW; Bao XH; Qin J; Wu XR
    Chin Med J (Engl); 2006 Mar; 119(5):373-7. PubMed ID: 16542579
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel mitochondrial DNA 8597T>C mutation of Leigh syndrome: report of one case.
    Tsai JD; Liu CS; Tsao TF; Sheu JN
    Pediatr Neonatol; 2012 Feb; 53(1):60-2. PubMed ID: 22348497
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Leigh syndrome with spinal cord involvement due to a hemizygous NDUFA1 mutation.
    Miyauchi A; Osaka H; Nagashima M; Kuwajima M; Monden Y; Kohda M; Kishita Y; Okazaki Y; Murayama K; Ohtake A; Yamagata T
    Brain Dev; 2018 Jun; 40(6):498-502. PubMed ID: 29506883
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency.
    Chol M; Lebon S; Bénit P; Chretien D; de Lonlay P; Goldenberg A; Odent S; Hertz-Pannier L; Vincent-Delorme C; Cormier-Daire V; Rustin P; Rötig A; Munnich A
    J Med Genet; 2003 Mar; 40(3):188-91. PubMed ID: 12624137
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T>C mutation.
    Ronchi D; Bordoni A; Cosi A; Rizzuti M; Fassone E; Di Fonzo A; Servida M; Sciacco M; Collotta M; Ronzoni M; Lucchini V; Mattioli M; Moggio M; Bresolin N; Corti S; Comi GP
    Biochem Biophys Res Commun; 2011 Aug; 412(2):245-8. PubMed ID: 21819970
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.