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Journal Abstract Search

433 related items for PubMed ID: 23772060

  • 1. 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
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  • 2. 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
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  • 3. 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 05; 119(5):373-7. PubMed ID: 16542579
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  • 4. Mitochondrial DNA mutations in late-onset Leigh syndrome.
    Wei Y, Cui L, Peng B.
    J Neurol; 2018 Oct 05; 265(10):2388-2395. PubMed ID: 30128709
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  • 5. 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 05; 36(9):807-12. PubMed ID: 24262866
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  • 6. 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 05; 30(2):265. PubMed ID: 17323145
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  • 8. Mild clinical manifestation and unusual recovery upon coenzyme Q₁₀ treatment in the first Chinese Leigh syndrome pedigree with mutation m.10197 G>A.
    Chen Z, Zhao Z, Ye Q, Chen Y, Pan X, Sun B, Huang H, Zheng A.
    Mol Med Rep; 2015 Mar 05; 11(3):1956-62. PubMed ID: 25384404
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  • 10. Cytochrome c oxidase partial deficiency-associated Leigh disease presenting as an extrapyramidal syndrome.
    Cacić M, Wilichowski E, Mejaski-Bosnjak V, Fumić K, Lujić L, Marusić Della Marina B, Hanefeld F.
    J Child Neurol; 2001 Aug 05; 16(8):616-9. PubMed ID: 11510939
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  • 11. The neuroimaging of Leigh syndrome: case series and review of the literature.
    Bonfante E, Koenig MK, Adejumo RB, Perinjelil V, Riascos RF.
    Pediatr Radiol; 2016 Apr 05; 46(4):443-51. PubMed ID: 26739140
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  • 12. [The molecular background of Leigh syndrome].
    Piekutowska-Abramczuk D.
    Neurol Neurochir Pol; 2008 Apr 05; 42(3):238-50. PubMed ID: 18651330
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  • 16. 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 05; 53(1):60-2. PubMed ID: 22348497
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  • 17. Unusual findings in Leigh syndrome caused by T8993C mutation.
    Yiş U, Seneca S, Dirik E, Kurul SH, Ozer E, Cakmakçi H, De Meirleir L.
    Eur J Paediatr Neurol; 2009 Nov 05; 13(6):550-2. PubMed ID: 19046652
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  • 19. Adult onset Leigh syndrome with mitochondrial DNA 8344 A>G mutation.
    Han JY, Sung JJ, Park HK, Yoon BN, Lee KW.
    J Clin Neurosci; 2014 Nov 05; 21(11):2009-11. PubMed ID: 24961732
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  • 20. 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 05; 43(4):819-826. PubMed ID: 31967322
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