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Journal Abstract Search

150 related items for PubMed ID: 1714114

  • 21. Diagnostic algorithm for familial chylomicronemia syndrome.
    Stroes E, Moulin P, Parhofer KG, Rebours V, Löhr JM, Averna M.
    Atheroscler Suppl; 2017 Jan; 23():1-7. PubMed ID: 27998715
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  • 23. Pancreatitis risk in genetic subtypes of multifactorial chylomicronemia syndrome.
    Berberich AJ, Hegele RA.
    Atherosclerosis; 2024 May; 392():117528. PubMed ID: 38594114
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  • 25. Compound heterozygosity for a new (S259G) and a previously described (G188E) mutation in lipoprotein lipase (LpL) as a cause of chylomicronemia. Mutations in brief no. 183. Online.
    Evans D, Wendt D, Ahle S, Guerra A, Beisiegel U.
    Hum Mutat; 1998 May; 12(3):217. PubMed ID: 10660334
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  • 26. Familial chylomicronemia due to a circulating inhibitor of lipoprotein lipase activity.
    Brunzell JD, Miller NE, Alaupovic P, St Hilaire RJ, Wang CS, Sarson DL, Bloom SR, Lewis B.
    J Lipid Res; 1983 Jan; 24(1):12-9. PubMed ID: 6833877
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  • 27. Compound heterozygosity for frameshift mutations in the gene for lipoprotein lipase in a patient with early-onset chylomicronemia.
    Foubert L, De Gennes JL, Benlian P, Truffert J, Miao L, Hayden MR.
    Hum Mutat; 1998 Jan; Suppl 1():S141-4. PubMed ID: 9452069
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  • 29. Familial Chylomicronemia Syndrome With a Novel Homozygous LPL Mutation Identified in Three Siblings in Their 50s.
    Ueda M, Burke FM, Remaley AT, Hegele RA, Rader DJ, Dunbar RL.
    Ann Intern Med; 2020 Apr 07; 172(7):500-502. PubMed ID: 31739313
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  • 30. [53-year-old man with "lipemic" plasma and conspicuous skin eruptions].
    Merkel M.
    Dtsch Med Wochenschr; 2009 May 07; 134(20):1053-4. PubMed ID: 19421927
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  • 35. [Case of the familial form of hyperchylomicronemia].
    Gorbanev EA, Suchkova EN, Aleksandrov GA.
    Ter Arkh; 1986 May 07; 58(1):114-6. PubMed ID: 3961682
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  • 37. Lipoprotein lipase deficiency in an infant.
    Nampoothiri S, Radhakrishnan N, Schwentek A, Hoffmann MM.
    Indian Pediatr; 2011 Oct 07; 48(10):805-6. PubMed ID: 22080683
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