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11. Familial chylomicronemia caused by a novel type of mutation in the APOE-CI-CIV-CII gene cluster encompassing both the APOCII gene and the first APOCIV gene mutation: APOCII-CIV(Nijmegen). de Graaf J; Hoffer MJ; Stuyt PM; Frants RR; Stalenhoef AF Biochem Biophys Res Commun; 2000 Jul; 273(3):1084-7. PubMed ID: 10891375 [TBL] [Abstract][Full Text] [Related]
12. [Ketoacidosis with false hyponatremia and important hyperchylomicronemia (author's transl)]. Heim J; Peltier JL; Thomas R Sem Hop; 1981 Mar 18-25; 57(11-12):601-4. PubMed ID: 6261344 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. A neonatal case of apolipoprotein C-II deficiency. Ohno M; Ishibashi S; Nakao K; Nozue T; Nonomura K; Yamada N; Aburatani H; Shimano H; Murase T Eur J Pediatr; 1989 Apr; 148(6):550-2. PubMed ID: 2501098 [TBL] [Abstract][Full Text] [Related]
15. [Autoimmune chylomicronemia--pathogenesis and pathophysiology]. Matsuzawa Y; Kihara S; Kubo M; Tarui S Nihon Rinsho; 1990 Jun; 48(6):1344-50. PubMed ID: 2200900 [No Abstract] [Full Text] [Related]
16. Apolipoprotein C-II is a novel substrate for matrix metalloproteinases. Kim SY; Park SM; Lee ST Biochem Biophys Res Commun; 2006 Jan; 339(1):47-54. PubMed ID: 16314153 [TBL] [Abstract][Full Text] [Related]