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11. 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]
12. Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an "FCS score". Moulin P; Dufour R; Averna M; Arca M; Cefalù AB; Noto D; D'Erasmo L; Di Costanzo A; Marçais C; Alvarez-Sala Walther LA; Banach M; Borén J; Cramb R; Gouni-Berthold I; Hughes E; Johnson C; Pintó X; Reiner Ž; van Lennep JR; Soran H; Stefanutti C; Stroes E; Bruckert E Atherosclerosis; 2018 Aug; 275():265-272. PubMed ID: 29980054 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. [Lipoprotein lipase: a multifunctional enzyme in lipoprotein metabolism]. Foubert L; Benlian P; Turpin G Presse Med; 1996 Feb; 25(5):207-10. PubMed ID: 8729382 [TBL] [Abstract][Full Text] [Related]
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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]
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20. Insulin sensitivity is impaired in heterozygous carriers of lipoprotein lipase deficiency. Hölzl B; Iglseder B; Sandhofer A; Malaimare L; Lang J; Paulweber B; Sandhofer F Diabetologia; 2002 Mar; 45(3):378-84. PubMed ID: 11914743 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]