These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
13. Apolipoprotein C-II deficiency presenting as a lipid encephalopathy in infancy. Wilson CJ; Priore Oliva C; Maggi F; Catapano AL; Calandra S Ann Neurol; 2003 Jun; 53(6):807-10. PubMed ID: 12783430 [TBL] [Abstract][Full Text] [Related]
14. Familial chylomicronemia due to a circulating inhibitor of lipoprotein lipase activity. Brunzell JD; Miller NE; Alaupovic P; St Hilaire RJ; Wang CS; Sarson DL; Bloom SR; Lewis B J Lipid Res; 1983 Jan; 24(1):12-9. PubMed ID: 6833877 [TBL] [Abstract][Full Text] [Related]
17. [Lipoprotein lipase deficiency. A familial study]. Vidal Serra J; Ferrer Codina I; Amat Ballarín L; Reina del Pozo M; Varea Calderón V; Llovera Pons M; Llorén Jove E; Aguilar Tellés E; Farré Masip C An Esp Pediatr; 1990 Sep; 33(3):293-5. PubMed ID: 2285199 [No Abstract] [Full Text] [Related]
18. Apolipoprotein C-II Tuzla: a novel large deletion in APOC2 caused by Alu-Alu homologous recombination in an infant with apolipoprotein C-II deficiency. Okubo M; Toromanovic A; Ebara T; Murase T Clin Chim Acta; 2015 Jan; 438():148-53. PubMed ID: 25172036 [TBL] [Abstract][Full Text] [Related]