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PUBMED FOR HANDHELDS

Journal Abstract Search


204 related items for PubMed ID: 29534878

  • 1. Roundtable discussion: Familial chylomicronemia syndrome: Diagnosis and management.
    Brown WV, Goldberg I, Duell B, Gaudet D.
    J Clin Lipidol; 2018; 12(2):254-263. PubMed ID: 29534878
    [Abstract] [Full Text] [Related]

  • 2. Challenges in familial chylomicronemia syndrome diagnosis and management across Latin American countries: An expert panel discussion.
    Santos RD, Lorenzatti A, Corral P, Nogueira JP, Cafferata AM, Aimone D, Lourenço CM, Izar MC, Lima JG, Lottenberg AM, Alonso R, Garay K, Morales AR, Vargas-Uricoechea H, Peña CAC, Roman-González A.
    J Clin Lipidol; 2021; 15(5):620-624. PubMed ID: 34920815
    [Abstract] [Full Text] [Related]

  • 3. [Chylomicronemia syndrome].
    Francis A, Levy Y.
    Harefuah; 2002 Feb; 141(2):201-3, 221, 220. PubMed ID: 11905095
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  • 4. Molecular and functional characterization of familial chylomicronemia syndrome.
    Teramoto R, Tada H, Kawashiri MA, Nohara A, Nakahashi T, Konno T, Inazu A, Mabuchi H, Yamagishi M, Hayashi K.
    Atherosclerosis; 2018 Feb; 269():272-278. PubMed ID: 29153744
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  • 7. Chylomicronemia syndrome. Interaction of genetic and acquired hypertriglyceridemia.
    Brunzell JD, Bierman EL.
    Med Clin North Am; 1982 Mar; 66(2):455-68. PubMed ID: 7040847
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  • 8. [Chylomicronemia syndrome--pathophysiology, clinical aspects and therapy].
    Klör HU.
    Klin Wochenschr; 1990 Mar; 68 Suppl 22():68-75. PubMed ID: 2087083
    [No Abstract] [Full Text] [Related]

  • 9. Analyses of familial chylomicronemia syndrome in Pereira, Colombia 2010-2020: a cross-sectional study.
    Rodriguez FH, Estrada JM, Quintero HMA, Nogueira JP, Porras-Hurtado GL.
    Lipids Health Dis; 2023 Mar 28; 22(1):43. PubMed ID: 36978188
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  • 13. 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 28; 35(2):125-30. PubMed ID: 11983347
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  • 15. Transient lipoprotein lipase deficiency with hyperchylomicronemia.
    Goldberg IJ, Paterniti JR, Franklin BH, Ginsberg HN, Ginsberg-Fellner F, Brown WV.
    Am J Med Sci; 1983 Mar 28; 286(2):28-31. PubMed ID: 6614044
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  • 16. [Chylomicronemia].
    Yamamoto T, Kawakami M.
    Nihon Rinsho; 1990 Nov 28; 48(11):2526-31. PubMed ID: 2270016
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  • 17. A Comprehensive Update on the Chylomicronemia Syndrome.
    Goldberg RB, Chait A.
    Front Endocrinol (Lausanne); 2020 Nov 28; 11():593931. PubMed ID: 33193106
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  • 18. Treatment of primary chylomicronemia due to familial hypertriglyceridemia by omega-3 fatty acids.
    Richter WO, Jacob BG, Ritter MM, Schwandt P.
    Metabolism; 1992 Oct 28; 41(10):1100-5. PubMed ID: 1406295
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  • 19. Familial chylomicronemia syndrome: A rare but devastating autosomal recessive disorder characterized by refractory hypertriglyceridemia and recurrent pancreatitis.
    Chyzhyk V, Brown AS.
    Trends Cardiovasc Med; 2020 Feb 28; 30(2):80-85. PubMed ID: 31003756
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  • 20. Chylomicronemia: Differences between familial chylomicronemia syndrome and multifactorial chylomicronemia.
    Paquette M, Bernard S, Hegele RA, Baass A.
    Atherosclerosis; 2019 Apr 28; 283():137-142. PubMed ID: 30655019
    [Abstract] [Full Text] [Related]


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