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Journal Abstract Search

196 related items for PubMed ID: 9590082

  • 1. [Carnitine palmitoyltransferase I(CPT1) deficiency].
    Yorifuji S.
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):401-2. PubMed ID: 9590082
    [No Abstract] [Full Text] [Related]

  • 2. [Carnitine transporter defect].
    Yorifuji S.
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):398-400. PubMed ID: 9590081
    [No Abstract] [Full Text] [Related]

  • 3. A novel mutation identified in carnitine palmitoyltransferase II deficiency.
    Yang BZ, Ding JH, Roe D, Dewese T, Day DW, Roe CR.
    Mol Genet Metab; 1998 Feb; 63(2):110-5. PubMed ID: 9562964
    [Abstract] [Full Text] [Related]

  • 4. [Carnitine palmitoyltransferase II(CPT2) deficiency].
    Yorifuji S.
    Ryoikibetsu Shokogun Shirizu; 1998 Feb; (18 Pt 1):405-6. PubMed ID: 9590084
    [No Abstract] [Full Text] [Related]

  • 5. [Carnitine palmitoyltransferase deficiency].
    Yorifuji S.
    Ryoikibetsu Shokogun Shirizu; 2001 Feb; (36):54-6. PubMed ID: 11596449
    [No Abstract] [Full Text] [Related]

  • 6. Serious pregnancy complications in a patient with previously undiagnosed carnitine palmitoyltransferase 1 deficiency.
    Ylitalo K, Vänttinen T, Halmesmäki E, Tyni T.
    Am J Obstet Gynecol; 2005 Jun; 192(6):2060-2. PubMed ID: 15970898
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  • 11. [Carnitine palmitoyltransferase I deficiency].
    Yorifuji S.
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():710-1. PubMed ID: 12013979
    [No Abstract] [Full Text] [Related]

  • 12. [Carnitine palmitoyltransferase deficiency: fatty acid utilization defect causing myopathy].
    Lehtonen A, Paljärvi L, Falck B, Somer H, Kalimo H.
    Duodecim; 1983 Apr; 99(16):1063-9. PubMed ID: 6641545
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  • 13. Novel mutations in CPT 1A define molecular heterogeneity of hepatic carnitine palmitoyltransferase I deficiency.
    Bennett MJ, Boriack RL, Narayan S, Rutledge SL, Raff ML.
    Mol Genet Metab; 2004 May; 82(1):59-63. PubMed ID: 15110323
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  • 14. Identification of novel mutations in Spanish patients with muscle carnitine palmitoyltransferase II deficiency.
    Martín MA, Rubio JC, del Hoyo P, García A, Bustos F, Campos Y, Cabello A, Culebras JM, Arenas J.
    Hum Mutat; 2000 Jun; 15(6):579-80. PubMed ID: 10862092
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  • 15. Molecular basis of hepatic carnitine palmitoyltransferase I deficiency.
    IJlst L, Mandel H, Oostheim W, Ruiter JP, Gutman A, Wanders RJ.
    J Clin Invest; 1998 Aug 01; 102(3):527-31. PubMed ID: 9691089
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  • 19. [Lipid metabolism disorder in skeletal musculature (carnitine palmitoyltransferase deficiency) and paroxysmal myoglobinuria].
    Aver'ianov IuN, Aleksandrovskaia TN, Kal'nova LI, Morozova EA, Shaldaeva VV.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1980 Aug 01; 80(11):1623-8. PubMed ID: 6935889
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  • 20. Clinical features and new molecular findings in Carnitine Palmitoyltransferase II (CPT II) deficiency.
    Corti S, Bordoni A, Ronchi D, Musumeci O, Aguennouz M, Toscano A, Lamperti C, Bresolin N, Comi GP.
    J Neurol Sci; 2008 Mar 15; 266(1-2):97-103. PubMed ID: 17936304
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