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Journal Abstract Search

150 related items for PubMed ID: 1714114

  • 1. The molecular basis of familial chylomicronemia.
    Ameis D, Schotz C, Greten H.
    Z Gastroenterol Verh; 1991 Mar; 26():102-3. PubMed ID: 1714114
    [No Abstract] [Full Text] [Related]

  • 2. Familial chylomicronemia syndrome.
    Mohandas MK, Jemila J, Ajith Krishnan AS, George TT.
    Indian J Pediatr; 2005 Feb; 72(2):181. PubMed ID: 15758547
    [Abstract] [Full Text] [Related]

  • 3. A single Ser259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestry.
    Foubert L, Bruin T, De Gennes JL, Ehrenborg E, Furioli J, Kastelein J, Benlian P, Hayden M.
    Hum Mutat; 1997 Feb; 10(3):179-85. PubMed ID: 9298816
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  • 4. Familial chylomicronemia syndrome.
    Sugandhan S, Khandpur S, Sharma VK.
    Pediatr Dermatol; 2007 Feb; 24(3):323-5. PubMed ID: 17542893
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  • 5. A missense mutation (Trp86----Arg) in exon 3 of the lipoprotein lipase gene: a cause of familial chylomicronemia.
    Ishimura-Oka K, Faustinella F, Kihara S, Smith LC, Oka K, Chan L.
    Am J Hum Genet; 1992 Jun; 50(6):1275-80. PubMed ID: 1598907
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  • 6. [Familial lipoprotein lipase deficiency].
    Yoshida T, Gotoda T.
    Ryoikibetsu Shokogun Shirizu; 1998 Jun; (19 Pt 2):84-7. PubMed ID: 9645014
    [No Abstract] [Full Text] [Related]

  • 7. A novel missense (E163G) mutation in the catalytic subunit of lipoprotein lipase causes familial chylomicronemia.
    Wiebusch H, Funke H, Santer R, Richter W, Assmann G.
    Hum Mutat; 1996 Jun; 8(4):392. PubMed ID: 8956052
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  • 9. Molecular basis of familial chylomicronemia: mutations in the lipoprotein lipase and apolipoprotein C-II genes.
    Reina M, Brunzell JD, Deeb SS.
    J Lipid Res; 1992 Dec; 33(12):1823-32. PubMed ID: 1479292
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  • 10. [Chylomicronemia].
    Yamamoto T, Kawakami M.
    Nihon Rinsho; 1990 Nov; 48(11):2526-31. PubMed ID: 2270016
    [No Abstract] [Full Text] [Related]

  • 11. Chylomicronemia syndrome.
    Rao AG, Konda C, Jhamnani KK.
    Indian J Dermatol Venereol Leprol; 2009 Nov; 75(2):220. PubMed ID: 19293528
    [No Abstract] [Full Text] [Related]

  • 12. Familial chylomicronemia syndrome: a novel mutation in the lipoprotein lipase gene.
    Van Biervliet S, Vande Velde S, De Bruyne P, Callewaert B, Verloo P, De Bruyne R.
    Acta Gastroenterol Belg; 2024 Nov; 87(2):326-328. PubMed ID: 39210765
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  • 14. Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome.
    Lam CW, Yuen YP, Cheng WF, Chan YW, Tong SF.
    Clin Chim Acta; 2006 Feb; 364(1-2):256-9. PubMed ID: 16153625
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  • 15. 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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  • 19. 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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