Display Settings:

Format
Sort by

Send to:

Choose Destination

    Results: 3

    1.

    The removal from plasma of chylomicrons and remnants is reduced in heterozygous familial hypercholesterolemia subjects with identified LDL receptor mutations: study with artificial emulsions.

    Carneiro MM, Miname MH, Gagliardi AC, Pereira C, Pereira AC, Krieger JE, Maranhão RC, Santos RD.

    Atherosclerosis. 2012 Mar;221(1):268-74. Epub 2011 Dec 29.

    PMID:
    22257824
    [PubMed - in process]
    2.

    Molecular characterization of familial hypercholesterolemia in Spain.

    Palacios L, Grandoso L, Cuevas N, Olano-Martín E, Martinez A, Tejedor D, Stef M.

    Atherosclerosis. 2012 Mar;221(1):137-42. Epub 2011 Dec 23.

    PMID:
    22244043
    [PubMed - in process]
    3.

    Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia.

    Surendran RP, Visser ME, Heemelaar S, Wang J, Peter J, Defesche JC, Kuivenhoven JA, Hosseini M, Péterfy M, Kastelein JJ, Johansen CT, Hegele RA, Stroes ES, Dallinga-Thie GM.

    J Intern Med. 2012 Jan 12. doi: 10.1111/j.1365-2796.2012.02516.x. [Epub ahead of print]

    PMID:
    22239554
    [PubMed - as supplied by publisher]

      Display Settings:

      Format
      Sort by

      Send to:

      Choose Destination

      Supplemental Content

      Find related data

      Recent activity

      Your browsing activity is empty.

      Activity recording is turned off.

      Turn recording back on

      See more...
      Write to the Help Desk