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Journal Abstract Search

111 related items for PubMed ID: 15840743

  • 1. 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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  • 2. Characterization of a new case of autoimmune type I hyperlipidemia: long-term remission under immunosuppressive therapy.
    Pruneta V, Moulin P, Labrousse F, Bondon PJ, Ponsin G, Berthezene F.
    J Clin Endocrinol Metab; 1997 Mar; 82(3):791-6. PubMed ID: 9062484
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  • 3. Prevalence and function of anti-lipoprotein lipase auto-antibodies in type V hyperchylomicronemia.
    Moret M, Pruneta-Deloche V, Sassolas A, Marcais C, Moulin P.
    Atherosclerosis; 2010 Feb; 208(2):324-7. PubMed ID: 19695572
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  • 6. Identification of compound heterozygous mutations (G188E/W382X) of lipoprotein lipase gene in a Japanese infant with hyperchylomicronemia: the G188E mutation was newly identified in Japanese.
    Takagi A, Ikeda Y, Tachi K, Shinozuka T, Yamamoto A.
    Clin Chim Acta; 1999 Jul; 285(1-2):143-54. PubMed ID: 10481930
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  • 12. Familial lipoprotein lipase deficiency: a case of compound heterozygosity of a novel duplication (R44Kfs*4) and a common mutation (N291S) in the lipoprotein lipase gene.
    Overgaard M, Brasen CL, Svaneby D, Feddersen S, Nybo M.
    Ann Clin Biochem; 2013 Jul; 50(Pt 4):374-9. PubMed ID: 23761384
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  • 16. The clinical, biochemical, and familial presentation of type V hyperlipoproteinemia in childhood.
    Kwiterovich PO, Farah JR, Brown WV, Bachorik PS, Baylin SB, Neill CA.
    Pediatrics; 1977 Apr; 59(4):513-25. PubMed ID: 191790
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  • 17. 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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  • 18. Recurrent acute and chronic pancreatitis in two brothers with familial chylomicronemia syndrome.
    Truninger K, Schmid PA, Hoffmann MM, Bertschinger P, Ammann RW.
    Pancreas; 2006 Mar; 32(2):215-9. PubMed ID: 16552344
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  • 19. GPIHBP1 C89F neomutation and hydrophobic C-terminal domain G175R mutation in two pedigrees with severe hyperchylomicronemia.
    Charrière S, Peretti N, Bernard S, Di Filippo M, Sassolas A, Merlin M, Delay M, Debard C, Lefai E, Lachaux A, Moulin P, Marçais C.
    J Clin Endocrinol Metab; 2011 Oct; 96(10):E1675-9. PubMed ID: 21816778
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