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Journal Abstract Search

191 related items for PubMed ID: 24113355

  • 21.
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  • 22. 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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  • 23. 3-methylglutaconic aciduria type 4 manifesting as Leigh syndrome in 2 siblings.
    Jareño NM, Fernández-Mayoralas DM, Silvestre CP, Cortés BM, Pérez MU, Campos-Castelló J.
    J Child Neurol; 2007 Feb 05; 22(2):218-21. PubMed ID: 17621487
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  • 26. Urinary titin as a biomarker in Fukuyama congenital muscular dystrophy.
    Sato T, Awano H, Ishiguro K, Shichiji M, Murakami T, Shirakawa T, Matsuo M, Nagata S, Ishigaki K.
    Neuromuscul Disord; 2021 Mar 05; 31(3):194-197. PubMed ID: 33563515
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  • 30. [Dystonia as a principal manifestation of Leigh syndrome in an infant].
    Muñoz Hiraldo ME, Martínez Bermejo A, Gutiérrez Molina M, García Melián RM, Arcas Martínez J, Pascual-Castroviejo I.
    An Esp Pediatr; 1993 Apr 05; 38(4):348-50. PubMed ID: 8480948
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  • 31. Case records of the Massachusetts General Hospital. Case 28-2008. An 8-day-old infant with congenital deafness, lethargy, and hypothermia.
    Staley KJ, Sims KB, Grant PE, Hedley-Whyte ET.
    N Engl J Med; 2008 Sep 11; 359(11):1156-67. PubMed ID: 18784106
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  • 37. [Recent progress, genetic diagnosis and its problem on congenital muscular dystrophies (Fukuyama and non-Fukuyama types)].
    Toda T.
    Rinsho Shinkeigaku; 1995 Dec 11; 35(12):1419-21. PubMed ID: 8752416
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  • 39. Mitochondrial DNA 8993T>G mutation in a child with ornithine transcarbamylase deficiency and leigh syndrome: an unexpected association.
    Henriques M, Diogo L, Garcia P, Pratas J, Simões M, Grazina M.
    J Child Neurol; 2012 Aug 11; 27(8):1059-61. PubMed ID: 22241703
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