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Journal Abstract Search
165 related items for PubMed ID: 3736552
1. Pathogenesis of type I hyperlipoproteinemia. Gnasso A, Koch H, Haberbosch W, Fellin R, Postiglione A, Augustin J. Monogr Atheroscler; 1986; 14():135-9. PubMed ID: 3736552 [No Abstract] [Full Text] [Related]
6. 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 06; 30(9):919-26. PubMed ID: 7266379 [Abstract] [Full Text] [Related]
7. Chylomicron and very-low-density lipoprotein levels in type I hyperlipoproteinaemia. The role of the liver in determining biochemical phenotype. Berger GM, Van der Westhuyzen JH, Huskisson J, Bonnici F, Henderson HE. S Afr Med J; 1982 Feb 20; 61(8):266-72. PubMed ID: 7058458 [Abstract] [Full Text] [Related]
8. [Hyperlipoproteinemia type I]. Bustos P, Fernández E, Radrigán E. Rev Chil Pediatr; 1987 Feb 20; 58(6):481-4. PubMed ID: 3506219 [No Abstract] [Full Text] [Related]
12. Studies of a variant very-low-density lipoprotein with an acquired deficiency of apolipoprotein C-II. Reckless JP, Stocks J, Holdsworth G, Galton DJ, Suggett AJ, Walton KW. Clin Sci (Lond); 1982 Jan 20; 62(1):93-100. PubMed ID: 7056035 [Abstract] [Full Text] [Related]
13. [Cholesterol and triglyceride content of lipoproteins in hyperlipoproteinemia type II/a, II/b and IV]. Romics L, Karádi I, Simonyi E. Orv Hetil; 1980 Oct 26; 121(43):2629-31. PubMed ID: 7208011 [No Abstract] [Full Text] [Related]
15. Compound heterozygosity for a known (D250N) and a novel (E410K) missense mutation in the C-terminal domain of lipoprotein lipase causes familial chylomicronemia. Wiebusch H, Funke H, Bruin T, Bucher H, von Eckardstein A, Kastelein JJ, Assmann G. Hum Mutat; 1996 Oct 26; 8(4):381-3. PubMed ID: 8956048 [No Abstract] [Full Text] [Related]
16. [Familial hyperchylomicronemia syndrome]. Tada N. Nihon Rinsho; 2001 Mar 26; 59 Suppl 3():13-21. PubMed ID: 11347044 [No Abstract] [Full Text] [Related]
19. Lipoprotein lipase with a defect in lipid interface recognition in a case with type I hyperlipidaemia. Kobayashi J, Shirai K, Saito Y, Yoshida S. Eur J Clin Invest; 1989 Oct 26; 19(5):424-32. PubMed ID: 2511018 [Abstract] [Full Text] [Related]
20. Familial apolipoprotein CII deficiency: plasma lipoproteins and apolipoproteins in heterozygous and homozygous subjects and the effects of plasma infusion. Miller NE, Rao SN, Alaupovic P, Noble N, Slack J, Brunzell JD, Lewis B. Eur J Clin Invest; 1981 Feb 26; 11(1):69-76. PubMed ID: 6783432 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]