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Journal Abstract Search

175 related items for PubMed ID: 21752325

  • 1. [Leigh syndrome due to mitochondrial respiratory chain complex II deficiency].
    Ma YY, Wu TF, Liu YP, Wang Q, Song JQ, Xiao JX, Jiang YW, Yang YL.
    Zhongguo Dang Dai Er Ke Za Zhi; 2011 Jul; 13(7):569-72. PubMed ID: 21752325
    [Abstract] [Full Text] [Related]

  • 2. [A case of Leigh syndrome associated with respiratory chain complex I deficiency due to mitochondrial gene 13513G>A mutation].
    Wei XQ, Kong QP, Zhang Y, Yang YL, Chang XZ, Qi Y, Qi ZY, Xiao JX, Qin J, Wu XR.
    Zhongguo Dang Dai Er Ke Za Zhi; 2009 May; 11(5):333-6. PubMed ID: 19470250
    [Abstract] [Full Text] [Related]

  • 3. [Intrahepatic cholestasis due to mitochondrial respiratory chain complex I deficiency in a Chinese boy].
    Wu TF, Liu YP, Wang Q, Li XY, Ma YY, Song JQ, Yang YL.
    Zhongguo Dang Dai Er Ke Za Zhi; 2012 Apr; 14(4):241-6. PubMed ID: 22537948
    [Abstract] [Full Text] [Related]

  • 4. Mitochondrial respiratory chain enzyme assay and DNA analysis in peripheral blood leukocytes for the etiological study of Chinese children with Leigh syndrome due to complex I deficiency.
    Ma YY, Wu TF, Liu YP, Wang Q, Li XY, Zhang Y, Song JQ, Wang YJ, Yang YL.
    Mitochondrial DNA; 2013 Feb; 24(1):67-73. PubMed ID: 22947169
    [Abstract] [Full Text] [Related]

  • 5. [Enzyme analysis of isolated mitochondrial respiratory chain complex III deficiency].
    Ma YY, Wu TF, Liu YP, Wang Q, Song JQ, Xiao JX, Jiang YW, Yang YL.
    Zhonghua Er Ke Za Zhi; 2011 Nov; 49(11):848-52. PubMed ID: 22336309
    [Abstract] [Full Text] [Related]

  • 6. [Mitochondrial respiratory chain complex I deficiency due to 10191T>C mutation in ND3 gene].
    Liu YP, Ma YY, Wu TF, Wang Q, Kong QP, Wei XQ, Zhang Y, Song JQ, Chang XZ, Zhang YH, Xiao JX, Yang YL.
    Zhongguo Dang Dai Er Ke Za Zhi; 2012 Aug; 14(8):561-6. PubMed ID: 22898272
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  • 8. [Leigh syndrome due to pyruvate dehydrogenase E1 alpha subunit gene mutation: a complicated and difficult case study].
    Zhang Y, Sun F, Yang YL, Chang XZ, Qi Y, Qi ZY, Xiao JX, Qin J, Wu XR.
    Zhongguo Dang Dai Er Ke Za Zhi; 2007 Jun; 9(3):216-9. PubMed ID: 17582259
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  • 10. Deficiency of respiratory chain complex I is a common cause of Leigh disease.
    Morris AA, Leonard JV, Brown GK, Bidouki SK, Bindoff LA, Woodward CE, Harding AE, Lake BD, Harding BN, Farrell MA, Bell JE, Mirakhur M, Turnbull DM.
    Ann Neurol; 1996 Jul; 40(1):25-30. PubMed ID: 8687187
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  • 12. Leigh syndrome: clinical features and biochemical and DNA abnormalities.
    Rahman S, Blok RB, Dahl HH, Danks DM, Kirby DM, Chow CW, Christodoulou J, Thorburn DR.
    Ann Neurol; 1996 Mar; 39(3):343-51. PubMed ID: 8602753
    [Abstract] [Full Text] [Related]

  • 13. [Complex II deficiency due to Fp gene mutation].
    Ito M.
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():444-5. PubMed ID: 12013908
    [No Abstract] [Full Text] [Related]

  • 14. [Mitochondrial respiratory chain complex Ⅱ deficiency and diseases].
    Ma YY, Yang YL.
    Zhongguo Dang Dai Er Ke Za Zhi; 2012 Oct; 14(10):723-7. PubMed ID: 23092560
    [Abstract] [Full Text] [Related]

  • 15. Mitochondrial tRNA gene mutations in patients having mitochondrial disease with lactic acidosis.
    Ueki I, Koga Y, Povalko N, Akita Y, Nishioka J, Yatsuga S, Fukiyama R, Matsuishi T.
    Mitochondrion; 2006 Feb; 6(1):29-36. PubMed ID: 16337222
    [Abstract] [Full Text] [Related]

  • 16. Stroke due to mitochondrial disorders in Saudi children.
    Salih MA, Abdel-Gader AG, Zahraa JN, Al-Rayess MM, Alorainy IA, Hassan HH, Ruitenbeek W, Zeviani M.
    Saudi Med J; 2006 Mar; 27 Suppl 1():S81-90. PubMed ID: 16532135
    [Abstract] [Full Text] [Related]

  • 17. Leigh disease with brainstem involvement in complex I deficiency due to assembly factor NDUFAF2 defect.
    Herzer M, Koch J, Prokisch H, Rodenburg R, Rauscher C, Radauer W, Forstner R, Pilz P, Rolinski B, Freisinger P, Mayr JA, Sperl W.
    Neuropediatrics; 2010 Feb; 41(1):30-4. PubMed ID: 20571988
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  • 20. [Mitochondrial leukoencephalopathy of infancy: is it an early expression of Leigh syndrome?].
    Rouco Axpe I, Garaizar Axpe C, Labairu Echevarría M, Sanjurjo Crespo P, Aldamiz Echevarría L, Prats Viñas JM.
    Neurologia; 2003 Jun; 18(5):241-7. PubMed ID: 12768509
    [Abstract] [Full Text] [Related]

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