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Journal Abstract Search

152 related items for PubMed ID: 21046879

  • 21. [Diagnostic value of mitochondrial DNA analysis in chronic progressive external ophthalmoplegia (CPEO)].
    Kornblum C, Kunz WS, Klockgether T, Roggenkämper P, Schröder R.
    Klin Monbl Augenheilkd; 2004 Dec; 221(12):1057-61. PubMed ID: 15599814
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  • 22. Mitochondrial abnormalities in muscle and other aging cells: classification, causes, and effects.
    DiMauro S, Tanji K, Bonilla E, Pallotti F, Schon EA.
    Muscle Nerve; 2002 Nov; 26(5):597-607. PubMed ID: 12402281
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  • 23. Mitochondrial diseases.
    Vu TH, Hirano M, DiMauro S.
    Neurol Clin; 2002 Aug; 20(3):809-39, vii-viii. PubMed ID: 12432831
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  • 24. [Mitochondrial syndrome].
    Kozłowska I, Rózański J, Ciechanowski K.
    Pol Merkur Lekarski; 2004 Oct; 17(100):395-8. PubMed ID: 15690713
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  • 25. Differential occurrence of mutations in mitochondrial DNA of human skeletal muscle during aging.
    Zhang C, Liu VW, Addessi CL, Sheffield DA, Linnane AW, Nagley P.
    Hum Mutat; 1998 Oct; 11(5):360-71. PubMed ID: 9600454
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  • 30. Quantification of changes in muscle from individuals with and without mitochondrial disease.
    Sleigh K, Ball S, Hilton DA.
    Muscle Nerve; 2011 Jun; 43(6):795-800. PubMed ID: 21607963
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  • 33. [Mitochondrial disorders].
    Munnich A, de Lonlay P, Rötig A, Rustin P.
    Bull Acad Natl Med; 2009 Jan; 193(1):19-41; discussion 41-3. PubMed ID: 19718979
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  • 39. Mitochondrial diseases--an expanding spectrum of disorders and affected genes.
    von Kleist-Retzow JC, Schauseil-Zipf U, Michalk DV, Kunz WS.
    Exp Physiol; 2003 Jan; 88(1):155-66. PubMed ID: 12525864
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  • 40. Probing striated muscle mitochondrial phenotype in neuromuscular disorders.
    Marín-García J, Goldenthal MJ, Sarnat HB.
    Pediatr Neurol; 2003 Jul; 29(1):26-33. PubMed ID: 13679118
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