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Journal Abstract Search

200 related items for PubMed ID: 35533124

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  • 7. Identification of a Compound Heterozygous LMF1 Variants in a Patient with Severe Hypertriglyceridemia - Case Report and Literature Review.
    Cao C, Liu Y, Liu L, Wang X.
    J Atheroscler Thromb; 2024 Jul 01; 31(7):1106-1111. PubMed ID: 38462482
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  • 10. 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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  • 11. 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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  • 15. Etiology and emerging treatments for familial chylomicronemia syndrome.
    Spagnuolo CM, Hegele RA.
    Expert Rev Endocrinol Metab; 2024 Jul 28; 19(4):299-306. PubMed ID: 38866702
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  • 17. A Comprehensive Update on the Chylomicronemia Syndrome.
    Goldberg RB, Chait A.
    Front Endocrinol (Lausanne); 2020 Jul 28; 11():593931. PubMed ID: 33193106
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  • 19. Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene.
    Kim KY, Heo YJ, Ko JM, Lee YA, Shin CH, Ki CS, Lee YJ.
    BMC Endocr Disord; 2024 Apr 15; 24(1):47. PubMed ID: 38622573
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  • 20. Genotype-phenotype relationships in patients with type I hyperlipoproteinemia.
    Chokshi N, Blumenschein SD, Ahmad Z, Garg A.
    J Clin Lipidol; 2014 Apr 15; 8(3):287-95. PubMed ID: 24793350
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