These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

130 related items for PubMed ID: 39210765

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23. Familial chylomicronemia syndrome caused by compound heterozygous mutation of lipoprotein lipase gene: A case report and review of literature.
    Huang Y, Qin Y, Liao L, Lin F.
    Clin Chim Acta; 2022 Dec 01; 537():112-117. PubMed ID: 36252692
    [Abstract] [Full Text] [Related]

  • 24. Two novel mutations of the LPL gene in two Chinese family cases with familial chylomicronemia syndrome.
    Wang M, Zhou Y, He X, Deng C, Liu X, Li J, Zhou L, Li Y, Zhang Y, Liu H, Li L.
    Clin Chim Acta; 2021 Oct 01; 521():264-271. PubMed ID: 34324844
    [Abstract] [Full Text] [Related]

  • 25. 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 01; 50(Pt 4):374-9. PubMed ID: 23761384
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. Homozygous LPL and GPIHBP1 variants causing familial chylomicronaemia syndrome in Sri Lankan children.
    Kiyamudeen F, Rajapaksha M, Atapattu N, Kularatne SD, Schröder S, Hooper AJ, Burnett JR, Jasinge E.
    Pathology; 2024 Oct 01; 56(6):904-906. PubMed ID: 38777740
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Familial chylomicronemia (type I hyperlipoproteinemia) due to a single missense mutation in the lipoprotein lipase gene.
    Ameis D, Kobayashi J, Davis RC, Ben-Zeev O, Malloy MJ, Kane JP, Lee G, Wong H, Havel RJ, Schotz MC.
    J Clin Invest; 1991 Apr 01; 87(4):1165-70. PubMed ID: 2010533
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. A new mutation in the human lipoprotein lipase gene causing familial hyperchylomicronaemia.
    Anwar R, Puntis JW, Markham AF.
    Mol Pathol; 1997 Aug 01; 50(4):221-3. PubMed ID: 9350308
    [Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. Lipoprotein abnormalities in compound heterozygous lipoprotein lipase deficiency after treatment with a low-fat diet and orlistat.
    Blackett P, Tryggestad J, Krishnan S, Li S, Xu W, Alaupovic P, Quiroga C, Copeland K.
    J Clin Lipidol; 2013 Aug 01; 7(2):132-9. PubMed ID: 23415432
    [Abstract] [Full Text] [Related]

  • 38. 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 01; 50(6):1275-80. PubMed ID: 1598907
    [Abstract] [Full Text] [Related]

  • 39. 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 01; 33(12):1823-32. PubMed ID: 1479292
    [Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 7.