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Journal Abstract Search

323 related items for PubMed ID: 17468530

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  • 6. Familial chylomicronemia syndrome.
    Mohandas MK, Jemila J, Ajith Krishnan AS, George TT.
    Indian J Pediatr; 2005 Feb; 72(2):181. PubMed ID: 15758547
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  • 8. [Chylomicronemia].
    Yamamoto T, Kawakami M.
    Nihon Rinsho; 1990 Nov; 48(11):2526-31. PubMed ID: 2270016
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  • 10. [Familial hyperchylomicronemia syndrome].
    Tada N.
    Nihon Rinsho; 2001 Mar; 59 Suppl 3():13-21. PubMed ID: 11347044
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  • 13. The familial hyperchylomicronaemia syndrome.
    Bijvoet SM, Bruin T, Kastelein JJ.
    Neth J Med; 1993 Feb; 42(1-2):36-44. PubMed ID: 8446222
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  • 14. Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome.
    Lam CW, Yuen YP, Cheng WF, Chan YW, Tong SF.
    Clin Chim Acta; 2006 Feb; 364(1-2):256-9. PubMed ID: 16153625
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  • 15. A Novel APOC2 Missense Mutation Causing Apolipoprotein C-II Deficiency With Severe Triglyceridemia and Pancreatitis.
    Ueda M, Dunbar RL, Wolska A, Sikora TU, Escobar MDR, Seliktar N, deGoma E, DerOhannessian S, Morrell L, McIntyre AD, Burke F, Sviridov D, Amar M, Shamburek RD, Freeman L, Hegele RA, Remaley AT, Rader DJ.
    J Clin Endocrinol Metab; 2017 May 01; 102(5):1454-1457. PubMed ID: 28201738
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  • 19. Familial Chylomicronemia Syndrome (FCS): Recent Data on Diagnosis and Treatment.
    Gallo A, Béliard S, D'Erasmo L, Bruckert E.
    Curr Atheroscler Rep; 2020 Aug 27; 22(11):63. PubMed ID: 32852651
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  • 20. [Chylomicronemia syndrome].
    Francis A, Levy Y.
    Harefuah; 2002 Feb 27; 141(2):201-3, 221, 220. PubMed ID: 11905095
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