Severe hypertriglyceridemia
Compound but non-linked heterozygous p.W14X and p.L279 V LPL gene mutations in a Chinese patient with long-term severe hypertriglyceridemia and recurrent acute pancreatitis
7
Management of severe hypertriglyceridemia due to lipoprotein lipase deficiency in children
5
Severe hypertriglyceridemia in a subject with disturbed life style and poor glycemic control without recurrence of acute pancreatitis: a case report
5
A novel APOC2 gene mutation identified in a Chinese patient with severe hypertriglyceridemia and recurrent pancreatitis
6
Frequency of rare mutations and common genetic variations in severe hypertriglyceridemia in the general population of Spain
8
A novel lipoprotein lipase gene missense mutation in Chinese patients with severe hypertriglyceridemia and pancreatitis
5
Identification of a novel and heterozygous LMF1 nonsense mutation in an acute pancreatitis patient with severe hypertriglyceridemia, severe obesity and heavy smoking
5
Update on the management of severe hypertriglyceridemia – focus on free fatty acid forms of omega-3
9
Severe hypertriglyceridemia, reduced high density lipoprotein, and neonatal death in lipoprotein lipase knockout mice Mild hypertriglyceridemia with impaired very low density lipoprotein clearance in heterozygotes
15
Incidence of pancreatitis, secondary causes, and treatment of patients referred to a specialty lipid clinic with severe hypertriglyceridemia: a retrospective cohort study
7
Icosapent ethyl for the treatment of severe hypertriglyceridemia
8
Severe hypertriglyceridemia in Norway: prevalence, clinical and genetic characteristics
8
Use of Plasmapheresis in Acute Pancreatitis Secondary to Hypertriglyceridemia
5
Lowering triglycerides to modify cardiovascular risk: will icosapent deliver?
7
Plasmapheresis to Treat Hypertriglyceridemia in a Child With Diabetic Ketoacidosis and Pancreatitis
6
Moderate Hypertriglyceridemia Revealed by Acute Chest Syndrome, a Milky Appearance Serum and Prior History of Recurrent Acute Pancreatitis in a Type 2 Diabetes Black Patient: A Case Report
8
A novel homozygous mutation in the glycerol-3-phosphate dehydrogenase 1 gene in a Chinese patient with transient infantile hypertriglyceridemia: a case report
8
Original Article Complement activation in the arteries of patients with severe atherosclerosis
9
CLEARANCE OF POSTPRANDIAL LIPIDS IS DELAYED IN SUBJECTS WITH CARDIOVASCULAR DISEASE
11
Metabolic Syndrome and Perioperative Complications during Scheduled Surgeries with Spinal Anesthesia
11