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6. 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]
7. The familial chylomicronemia syndrome. Santamarina-Fojo S Endocrinol Metab Clin North Am; 1998 Sep; 27(3):551-67, viii. PubMed ID: 9785052 [TBL] [Abstract][Full Text] [Related]
8. [Quantification of very low density lipoprotein apo C and apo E peptides by isoelectric focusing in type IV hyperlipidemia, familial chylomicronemia and xanthelasma palpebrae without hyperlipidemia (author's transl)]. Wada K; Miki H; Okuda F; Kusukawa R Nihon Ronen Igakkai Zasshi; 1981 Nov; 18(6):410-6. PubMed ID: 7339080 [No Abstract] [Full Text] [Related]
9. Molecular genetics of apoC-II and lipoprotein lipase deficiency. Fojo SS; de Gennes JL; Beisiegel U; Baggio G; Stalenhoef AF; Brunzell JD; Brewer HB Adv Exp Med Biol; 1991; 285():329-33. PubMed ID: 1858563 [No Abstract] [Full Text] [Related]
10. Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome. Lam CW; Yuen YP; Cheng WF; Chan YW; Tong SF Clin Chim Acta; 2006 Feb; 364(1-2):256-9. PubMed ID: 16153625 [TBL] [Abstract][Full Text] [Related]
11. Encephalopathy in type I hyperlipidemia. Onal H; Atugluzeybek C; Alhaj S; Altun G Indian Pediatr; 2007 Apr; 44(4):306-8. PubMed ID: 17468530 [TBL] [Abstract][Full Text] [Related]
15. Familial chylomicronemia in a nine months old infant. Lone SW; Imdad A; Billoo AG J Coll Physicians Surg Pak; 2008 Oct; 18(10):655-6. PubMed ID: 18940129 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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; 8(4):381-3. PubMed ID: 8956048 [No Abstract] [Full Text] [Related]
18. A single Ser259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestry. Foubert L; Bruin T; De Gennes JL; Ehrenborg E; Furioli J; Kastelein J; Benlian P; Hayden M Hum Mutat; 1997; 10(3):179-85. PubMed ID: 9298816 [TBL] [Abstract][Full Text] [Related]
19. The plasma lipoproteins in familial chylomicronemia. Analysis by zonal ultracentrifugation. Manzato E; Marin R; Gasparotto A; Baggio G; Fellin R; Crepaldi G J Lab Clin Med; 1984 Nov; 104(5):778-88. PubMed ID: 6491471 [TBL] [Abstract][Full Text] [Related]
20. The molecular basis of familial chylomicronemia. Ameis D; Schotz C; Greten H Z Gastroenterol Verh; 1991 Mar; 26():102-3. PubMed ID: 1714114 [No Abstract] [Full Text] [Related] [Next] [New Search]