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6. Successful pregnancy outcome in a patient with severe chylomicronemia due to compound heterozygosity for mutant lipoprotein lipase. Al-Shali K; Wang J; Fellows F; Huff MW; Wolfe BM; Hegele RA Clin Biochem; 2002 Mar; 35(2):125-30. PubMed ID: 11983347 [TBL] [Abstract][Full Text] [Related]
7. Management of patients with severe hypertriglyceridaemia during pregnancy: report of two cases with familial lipoprotein lipase deficiency. Watts GF; Morton K; Jackson P; Lewis B Br J Obstet Gynaecol; 1992 Feb; 99(2):163-6. PubMed ID: 1554674 [No Abstract] [Full Text] [Related]
8. 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]
9. [Chylomicronemia syndrome]. Francis A; Levy Y Harefuah; 2002 Feb; 141(2):201-3, 221, 220. PubMed ID: 11905095 [TBL] [Abstract][Full Text] [Related]
10. Familial chylomicronemia syndrome: Bringing to life dietary recommendations throughout the life span. Williams L; Rhodes KS; Karmally W; Welstead LA; Alexander L; Sutton L; J Clin Lipidol; 2018; 12(4):908-919. PubMed ID: 29804909 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Recurrent acute and chronic pancreatitis in two brothers with familial chylomicronemia syndrome. Truninger K; Schmid PA; Hoffmann MM; Bertschinger P; Ammann RW Pancreas; 2006 Mar; 32(2):215-9. PubMed ID: 16552344 [TBL] [Abstract][Full Text] [Related]