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Journal Abstract Search

196 related items for PubMed ID: 28201738

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  • 2. Apolipoprotein C-II deficiency with no rare variant in the APOC2 gene.
    Takase S, Osuga J, Fujita H, Hara K, Sekiya M, Igarashi M, Takanashi M, Takeuchi Y, Izumida Y, Ohta K, Kumagai M, Nishi M, Kubota M, Masuda Y, Taira Y, Okazaki S, Iizuka Y, Yahagi N, Ohashi K, Yoshida H, Yanai H, Tada N, Gotoda T, Ishibashi S, Kadowaki T, Okazaki H.
    J Atheroscler Thromb; 2013; 20(5):481-93. PubMed ID: 23470567
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  • 3. Familial Chylomicronemia Syndrome: A Clinical Guide For Endocrinologists.
    Falko JM.
    Endocr Pract; 2018 Aug; 24(8):756-763. PubMed ID: 30183397
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  • 5. Molecular analysis of three known and one novel LPL variants in patients with type I hyperlipoproteinemia.
    Caddeo A, Mancina RM, Pirazzi C, Russo C, Sasidharan K, Sandstedt J, Maurotti S, Montalcini T, Pujia A, Leren TP, Romeo S, Pingitore P.
    Nutr Metab Cardiovasc Dis; 2018 Feb; 28(2):158-164. PubMed ID: 29288010
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  • 8. Successful management of acute pancreatitis due to apolipoprotein C-II deficiency in a 37-day-old infant.
    Yıldız Y, Uysal Yazıcı M, Çınar HG, Özbay Hoşnut F, Kurt Çolak F, Kılıç M.
    Pancreatology; 2020 Jun; 20(4):644-646. PubMed ID: 32205061
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  • 9. Genotype-phenotype relationships in patients with type I hyperlipoproteinemia.
    Chokshi N, Blumenschein SD, Ahmad Z, Garg A.
    J Clin Lipidol; 2014 Jun; 8(3):287-95. PubMed ID: 24793350
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  • 10. Monogenic hypertriglyceridemia and recurrent pancreatitis in a homozygous carrier of a rare APOA5 mutation: a case report.
    Makhmudova U, Schulze PC, Lorkowski S, März W, Geiling JA, Weingärtner O.
    J Med Case Rep; 2024 Jun 14; 18(1):278. PubMed ID: 38872171
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  • 14. 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 14; 30(2):80-85. PubMed ID: 31003756
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  • 17. 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. Familial chylomicronemia syndrome: an under-recognized cause of severe hypertriglyceridaemia.
    Baass A, Paquette M, Bernard S, Hegele RA.
    J Intern Med; 2020 Apr 27; 287(4):340-348. PubMed ID: 31840878
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