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Journal Abstract Search

127 related items for PubMed ID: 23704442

  • 1. Persistent hyperlactacidaemia: about a clinical case.
    Oliveira AR, Valente R, Ramos J, Ventura L.
    BMJ Case Rep; 2013 May 22; 2013():. PubMed ID: 23704442
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  • 2. Leigh syndrome: pyruvate dehydrogenase defect. A case with peripheral neuropathy.
    Chabrol B, Mancini J, Benelli C, Gire C, Munnich A.
    J Child Neurol; 1994 Jan 22; 9(1):52-5. PubMed ID: 8151084
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  • 3. Proton spectroscopy in patients with Leigh's disease and mitochondrial enzyme deficiency.
    Kruse B, Hanefeld F, Holzbach U, Wilichowski E, Christen HJ, Merboldt KD, Hänicke W, Frahm J.
    Dev Med Child Neurol; 1994 Sep 22; 36(9):839-43. PubMed ID: 7926334
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  • 11. 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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  • 13. Leigh syndrome presenting with dystonia: report of one case.
    Huang WY, Chi CS, Mak SC, Wu HM, Yang MT.
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1995 Mar 05; 36(5):378-81. PubMed ID: 8607367
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  • 14. Assessment and therapy monitoring of Leigh disease by MRI and proton spectroscopy.
    Krägeloh-Mann I, Grodd W, Niemann G, Haas G, Ruitenbeek W.
    Pediatr Neurol; 1992 Mar 05; 8(1):60-4. PubMed ID: 1558578
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  • 17. [Leigh disease in a 3-year-old girl].
    Kałuza J, Krauze M, Marszał E, Wojczańska-Stanek K, Jamroz E, Szwed-Białozyt B.
    Neurol Neurochir Pol; 1991 Mar 05; 25(4):497-500. PubMed ID: 1803261
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