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Journal Abstract Search

215 related items for PubMed ID: 9785052

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  • 6. Familial chylomicronemia syndrome.
    Sugandhan S, Khandpur S, Sharma VK.
    Pediatr Dermatol; 2007; 24(3):323-5. PubMed ID: 17542893
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  • 9. Successful pregnancy outcome in a patient with severe chylomicronemia due to compound heterozygosity for mutant lipoprotein lipase.
    Al-Shali K, Wang J, Fellows F, Huff MW, Wolfe BM, Hegele RA.
    Clin Biochem; 2002 Mar; 35(2):125-30. PubMed ID: 11983347
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  • 10. Molecular basis of familial chylomicronemia: mutations in the lipoprotein lipase and apolipoprotein C-II genes.
    Reina M, Brunzell JD, Deeb SS.
    J Lipid Res; 1992 Dec; 33(12):1823-32. PubMed ID: 1479292
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  • 11. High frequency of mutations in the human lipoprotein lipase gene in pregnancy-induced chylomicronemia: possible association with apolipoprotein E2 isoform.
    Ma Y, Ooi TC, Liu MS, Zhang H, McPherson R, Edwards AL, Forsythe IJ, Frohlich J, Brunzell JD, Hayden MR.
    J Lipid Res; 1994 Jun; 35(6):1066-75. PubMed ID: 8077845
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  • 12. Hypertriglyceridaemia due to genetic defects in lipoprotein lipase and apolipoprotein C-II.
    Fojo SS, Brewer HB.
    J Intern Med; 1992 Jun; 231(6):669-77. PubMed ID: 1619390
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  • 17. Severe Hypertriglyceridemia due to a novel p.Q240H mutation in the Lipoprotein Lipase gene.
    Soto AG, McIntyre A, Agrawal S, Bialo SR, Hegele RA, Boney CM.
    Lipids Health Dis; 2015 Sep 04; 14():102. PubMed ID: 26337181
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  • 19. Chylomicronemia syndrome.
    Chait A, Brunzell JD.
    Adv Intern Med; 1992 Sep 04; 37():249-73. PubMed ID: 1557997
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  • 20. The Chylomicronemia Syndrome Is Most Often Multifactorial: A Narrative Review of Causes and Treatment.
    Chait A, Eckel RH.
    Ann Intern Med; 2019 May 07; 170(9):626-634. PubMed ID: 31035285
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