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PUBMED FOR HANDHELDS

Journal Abstract Search


201 related items for PubMed ID: 10658170

  • 1. Mitochondrial myopathy diagnosis.
    Shoffner JM.
    Neurol Clin; 2000 Feb; 18(1):105-23. PubMed ID: 10658170
    [Abstract] [Full Text] [Related]

  • 2. Mitochondrial myopathies and encephalomyopathies.
    Schapira AH, Cock HR.
    Eur J Clin Invest; 1999 Oct; 29(10):886-98. PubMed ID: 10583431
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  • 5. 163rd ENMC International Workshop: nucleoid and nucleotide biology in syndromes of mitochondrial DNA depletion myopathy 12-14 December 2008, Naarden, The Netherlands.
    Poulton J, Holt IJ.
    Neuromuscul Disord; 2009 Jun; 19(6):439-43. PubMed ID: 19464176
    [No Abstract] [Full Text] [Related]

  • 6. Clinical presentations and laboratory investigations in respiratory chain deficiency.
    Munnich A, Rötig A, Chretien D, Saudubray JM, Cormier V, Rustin P.
    Eur J Pediatr; 1996 Apr; 155(4):262-74. PubMed ID: 8777918
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  • 7. [Diagnostic investigations of mitochondrial diseases with neurological symptoms].
    Auré K, Lombès A.
    Rev Neurol (Paris); 2007 Feb; 163(2):254-63. PubMed ID: 17351548
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  • 8. Evoked potentials in the evaluation of patients with mitochondrial myopathy.
    Sartucci F, Rossi B, Tognoni G, Siciliano G, Guerrini V, Murri L.
    Eur Neurol; 1993 Feb; 33(6):428-35. PubMed ID: 8307064
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  • 10. Mitochondrial disorders.
    Schapira AH.
    Curr Opin Neurol; 1997 Feb; 10(1):43-7. PubMed ID: 9099526
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  • 14. Mitochondrial DNA mutations and mitochondrial dysfunction in epilepsy.
    Cock H, Schapira AH.
    Epilepsia; 1999 Feb; 40 Suppl 3():33-40. PubMed ID: 10446749
    [No Abstract] [Full Text] [Related]

  • 15. [Mitochondrial diseases].
    Pihko H, Suomalainen A, Somer H, Haltia M, Majander A.
    Duodecim; 1992 Feb; 108(6):578-90. PubMed ID: 1366118
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  • 16. [Mitochondrial diseases].
    Nagel JD, Haverkamp F, Lentze MJ.
    Klin Padiatr; 1997 Feb; 209(6):345-56. PubMed ID: 9445918
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  • 17. The genetics and pathology of oxidative phosphorylation.
    Smeitink J, van den Heuvel L, DiMauro S.
    Nat Rev Genet; 2001 May; 2(5):342-52. PubMed ID: 11331900
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  • 18. MRI in myopathy.
    Lovitt S, Marden FA, Gundogdu B, Ostrowski ML.
    Neurol Clin; 2004 Aug; 22(3):509-38, v. PubMed ID: 15207874
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  • 19. Altered skeletal muscle (mitochondrial) properties in patients with mitochondrial DNA single deletion myopathy.
    Gehrig SM, Mihaylova V, Frese S, Mueller SM, Ligon-Auer M, Spengler CM, Petersen JA, Lundby C, Jung HH.
    Orphanet J Rare Dis; 2016 Jul 29; 11(1):105. PubMed ID: 27473873
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  • 20. Maternal inheritance and the evaluation of oxidative phosphorylation diseases.
    Shoffner JM.
    Lancet; 1996 Nov 09; 348(9037):1283-8. PubMed ID: 8909383
    [Abstract] [Full Text] [Related]


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