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Journal Abstract Search

125 related items for PubMed ID: 6614044

  • 21. Long-term course of lipoprotein lipase (LPL) deficiency due to homozygous LPL(Arita) in a patient with recurrent pancreatitis, retained glucose tolerance, and atherosclerosis.
    Kawashiri MA, Higashikata T, Mizuno M, Takata M, Katsuda S, Miwa K, Nozue T, Nohara A, Inazu A, Kobayashi J, Koizumi J, Mabuchi H.
    J Clin Endocrinol Metab; 2005 Dec; 90(12):6541-4. PubMed ID: 16174715
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  • 23. Rare case of autoimmune hyperchylomicronemia during pregnancy.
    Yoshimura T, Ito M, Sakoda Y, Kobori S, Okamura H.
    Eur J Obstet Gynecol Reprod Biol; 1998 Jan; 76(1):49-51. PubMed ID: 9481547
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  • 24. Roundtable discussion: Familial chylomicronemia syndrome: Diagnosis and management.
    Brown WV, Goldberg I, Duell B, Gaudet D.
    J Clin Lipidol; 2018 Jan; 12(2):254-263. PubMed ID: 29534878
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  • 25. [Primary hyperchylomicronemia].
    Yamashita S.
    Nihon Rinsho; 2013 Sep; 71(9):1578-83. PubMed ID: 24205717
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  • 31. The plasma lipoproteins in familial chylomicronemia. Analysis by zonal ultracentrifugation.
    Manzato E, Marin R, Gasparotto A, Baggio G, Fellin R, Crepaldi G.
    J Lab Clin Med; 1984 Nov; 104(5):778-88. PubMed ID: 6491471
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  • 32. Adipose cell size and distribution in familial lipoprotein lipase deficiency.
    Peeva E, Brun LD, Ven Murthy MR, Després JP, Normand T, Gagné C, Lupien PJ, Julien P.
    Int J Obes Relat Metab Disord; 1992 Oct; 16(10):737-44. PubMed ID: 1330953
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  • 33. Pathogenesis of type I hyperlipoproteinemia.
    Gnasso A, Koch H, Haberbosch W, Fellin R, Postiglione A, Augustin J.
    Monogr Atheroscler; 1986 Oct; 14():135-9. PubMed ID: 3736552
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  • 36. 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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  • 37. [Case of the familial form of hyperchylomicronemia].
    Gorbanev EA, Suchkova EN, Aleksandrov GA.
    Ter Arkh; 1986 Feb; 58(1):114-6. PubMed ID: 3961682
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  • 38. Combination of circulating antilipoprotein lipase (Anti-LPL) antibody and heterozygous S172 fsX179 mutation of LPL gene leading to chronic hyperchylomicronemia.
    Pruneta-Deloche V, Marçais C, Perrot L, Sassolas A, Delay M, Estour B, Lagarde M, Moulin P.
    J Clin Endocrinol Metab; 2005 Jul; 90(7):3995-8. PubMed ID: 15840743
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  • 39. [Lipoprotein lipase deficiency. Apropos of 2 cases].
    Guyot A, Bost M, Groslambert P, Foulon T, Jeannoel P.
    Pediatrie; 1986 Jul; 41(1):33-9. PubMed ID: 3725507
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