BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 3630977)

  • 1. An incomplete form of familial lipoprotein lipase deficiency presenting with type I hyperlipoproteinemia.
    Berger GM
    Am J Clin Pathol; 1987 Sep; 88(3):369-73. PubMed ID: 3630977
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clearance defects in primary chylomicronemia: a study of tissue lipoprotein lipase activities.
    Berger GM
    Metabolism; 1986 Nov; 35(11):1054-61. PubMed ID: 3773723
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Combined deficiency of apolipoprotein C-II and lipoprotein lipase in familial hyperchylomicronemia.
    Stalenhoef AF; Casparie AF; Demacker PN; Stouten JT; Lutterman JA; van 't Laar A
    Metabolism; 1981 Sep; 30(9):919-26. PubMed ID: 7266379
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Postheparin plasma lipoprotein lipase activity in heterozygotes of familial lipoprotein lipase deficiency.
    Kondo Y; Kurobane I; Omura K; Sano R; Abe R; Chida N; Tada K
    Tohoku J Exp Med; 1985 Jan; 145(1):1-6. PubMed ID: 3983953
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hypertriglyceridaemia due to genetic defects in lipoprotein lipase and apolipoprotein C-II.
    Fojo SS; Brewer HB
    J Intern Med; 1992 Jun; 231(6):669-77. PubMed ID: 1619390
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hyperlipoproteinemia type I in a patient with active lipoprotein lipase in adipose tissue and indications of defective transport of the enzyme.
    Fager G; Semb H; Enerbäck S; Olivecrona T; Jonasson L; Bengtsson-Olivecrona G; Camejo G; Bjursell G; Bondjers G
    J Lipid Res; 1990 Jul; 31(7):1187-97. PubMed ID: 2205700
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Editorial commentary: Dietary management of familial chylomicronemia syndrome.
    Williams L; Wilson DP
    J Clin Lipidol; 2016; 10(3):462-5. PubMed ID: 27206931
    [No Abstract]   [Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Abnormal lipoprotein lipase in familial exogenous hypertriglyceridemia.
    Schreibman PH; Arons DL; Saudek CD; Arky RA
    J Clin Invest; 1973 Aug; 52(8):2075-82. PubMed ID: 4719678
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Primary type 1 hyperlipoproteinemia: significance of lipoprotein lipase and hepatic triglyceride lipase activity in heterozygotes of patients with familial lipoprotein lipase deficiency.
    Go T; Ohkubo H; Mochizuki Y; Murase T; Yamada N
    J Pediatr; 1983 Mar; 102(3):405-7. PubMed ID: 6827414
    [No Abstract]   [Full Text] [Related]  

  • 12. Transient lipoprotein lipase deficiency with hyperchylomicronemia.
    Goldberg IJ; Paterniti JR; Franklin BH; Ginsberg HN; Ginsberg-Fellner F; Brown WV
    Am J Med Sci; 1983; 286(2):28-31. PubMed ID: 6614044
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gene polymorphism identified by PvuII in familial lipoprotein lipase deficiency.
    Gotoda T; Senda M; Murase T; Yamada N; Takaku F; Furuichi Y
    Biochem Biophys Res Commun; 1989 Nov; 164(3):1391-6. PubMed ID: 2574035
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Postprandial adipose tissue lipoprotein lipase activity in primary hypertriglyceridemia.
    Goldberg AP; Chait A; Brunzell JD
    Metabolism; 1980 Mar; 29(3):223-9. PubMed ID: 7374436
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotypic heterogeneity in the extended pedigree of a proband with lipoprotein lipase deficiency.
    Wilson DE; Edwards CQ; Chan IF
    Metabolism; 1983 Dec; 32(12):1107-14. PubMed ID: 6645961
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial chylomicronemia syndrome.
    Sugandhan S; Khandpur S; Sharma VK
    Pediatr Dermatol; 2007; 24(3):323-5. PubMed ID: 17542893
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial type I hyperlipoproteinemia caused by apolipoprotein C-II deficiency.
    Yamamura T; Sudo H; Ishikawa K; Yamamoto A
    Atherosclerosis; 1979 Sep; 34(1):53-65. PubMed ID: 227429
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Chylomicronemia].
    Yamamoto T; Kawakami M
    Nihon Rinsho; 1990 Nov; 48(11):2526-31. PubMed ID: 2270016
    [No Abstract]   [Full Text] [Related]  

  • 20. Lipoprotein lipase deficiency in an infant.
    Nampoothiri S; Radhakrishnan N; Schwentek A; Hoffmann MM
    Indian Pediatr; 2011 Oct; 48(10):805-6. PubMed ID: 22080683
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.