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23. Underrecognition of chylomicronemia as a cause of acute pancreatitis. Searles GE; Ooi TC CMAJ; 1992 Dec; 147(12):1806-8. PubMed ID: 1458422 [TBL] [Abstract][Full Text] [Related]
30. [Disorders of lipid metabolism--diagnosis and therapy in general practice. 7: Treatment of increased triglycerides]. Richter WO Fortschr Med; 1996 Jun; 114(17):229-30. PubMed ID: 8767301 [No Abstract] [Full Text] [Related]
34. A Comprehensive Update on the Chylomicronemia Syndrome. Goldberg RB; Chait A Front Endocrinol (Lausanne); 2020; 11():593931. PubMed ID: 33193106 [TBL] [Abstract][Full Text] [Related]
35. The familial hyperchylomicronemia syndrome. New insights into underlying genetic defects. Santamarina-Fojo S; Brewer HB JAMA; 1991 Feb; 265(7):904-8. PubMed ID: 1992190 [No Abstract] [Full Text] [Related]
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37. 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]
38. Acute pancreatitis and hypertriglyceridemia. Lindberg DA Gastroenterol Nurs; 2009; 32(2):75-82; quiz 83-4. PubMed ID: 19357469 [TBL] [Abstract][Full Text] [Related]
39. Familial chylomicronemia syndrome: A rare but devastating autosomal recessive disorder characterized by refractory hypertriglyceridemia and recurrent pancreatitis. Chyzhyk V; Brown AS Trends Cardiovasc Med; 2020 Feb; 30(2):80-85. PubMed ID: 31003756 [TBL] [Abstract][Full Text] [Related]
40. Challenges in familial chylomicronemia syndrome diagnosis and management across Latin American countries: An expert panel discussion. Santos RD; Lorenzatti A; Corral P; Nogueira JP; Cafferata AM; Aimone D; Lourenço CM; Izar MC; Lima JG; Lottenberg AM; Alonso R; Garay K; Morales AR; Vargas-Uricoechea H; Peña CAC; Roman-González A J Clin Lipidol; 2021; 15(5):620-624. PubMed ID: 34920815 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]