Disease: Familial Lipoprotein Lipase Deficiency
- A case of hyperchylomicronemia associated with GPIHBP1 autoantibodies and fluctuating thyroid autoimmune disease
- A case of neonatal-onset type I hyperlipoproteinemia with bloody ascites
- A novel fully human anti-NT-ANGPTL3 antibody from phage display library exhibits potent ApoB, TG, and LDL-C lowering activities in hyperlipidemia mice
- Acute pancreatitis risk in multifactorial chylomicronemia syndrome depends on the molecular cause of severe hypertriglyceridemia
- Analyses of familial chylomicronemia syndrome in Pereira, Colombia 2010-2020: a cross-sectional study
- Apolipoprotein C-III, familial chylomicronemia syndrome, and olezarsen
- Biochemical, Clinical, and Genetic Characteristics of Mexican Patients with Primary Hypertriglyceridemia, Including the First Case of Hyperchylomicronemia Syndrome Due to GPIHBP1 Deficiency
- Brazilian Position Statement for Familial Chylomicronemia Syndrome - 2023
- Breaking the chains of lipoprotein lipase deficiency: A pediatric perspective on the efficacy and safety of Volanesorsen
- Clinical characterization and mutation spectrum of patients with hypertriglyceridemia in a German outpatient clinic
- Clinical practice recommendations on lipoprotein apheresis for children with homozygous familial hypercholesterolaemia: An expert consensus statement from ERKNet and ESPN
- Clinical profile, genetic spectrum and therapy evaluation of 19 Chinese pediatric patients with lipoprotein lipase deficiency
- Diagnosis and stabilisation of familial chylomicronemia syndrome in two infants presenting with hypertriglyceridemia-induced acute pancreatitis
- Distinguishing Lysosomal Acid Lipase Deficiency From Familial Hypercholesterolemia
- Etiology and emerging treatments for familial chylomicronemia syndrome
- Evinacumab in severe hypertriglyceridemia with or without lipoprotein lipase pathway mutations: a phase 2 randomized trial
- Exchange Transfusion: A Good Option for the Acute Treatment of Familial Chylomicronemia Syndrome in the Neonatal Period
- Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene
- Genetic and clinical characteristics of patients with lipoprotein lipase deficiency from Slovenia and Pakistan: case series and systematic literature review
- Genetic variation in apolipoprotein A-V in hypertriglyceridemia
- How ANGPTL3 Inhibition Will Help Our Clinical Practice?
- Identification of a Compound Heterozygous LMF1 Variants in a Patient with Severe Hypertriglyceridemia - Case Report and Literature Review
- Long-term clinical outcomes and management of hypertriglyceridemia in children with Apo-CII deficiency
- Long-term effects of volanesorsen on triglycerides and pancreatitis in patients with familial chylomicronaemia syndrome (FCS) in the UK Early Access to Medicines Scheme (EAMS)
- Long-Term Nutritional Counseling for a Patient with Lipoprotein Lipase Deficiency
- Long-Term Treatment of Lipoprotein Lipase Deficiency with Medium-Chain Triglyceride-Enriched Diet: A Case Series
- Monogenic hypertriglyceridemia and recurrent pancreatitis in a homozygous carrier of a rare APOA5 mutation: a case report
- Multifactorial chylomicronemia syndrome
- Novel pathogenic variant combination in <em>LPL</em> causing familial chylomicronemia syndrome in an Asian family and experimental validation <em>in vitro</em>: a case report
- Olezarsen, Acute Pancreatitis, and Familial Chylomicronemia Syndrome
- Pancreatitis polygenic risk score is associated with acute pancreatitis in multifactorial chylomicronemia syndrome
- Pancreatitis risk in genetic subtypes of multifactorial chylomicronemia syndrome
- Phase 1 Trials of PNPLA3 siRNA in I148M Homozygous Patients with MAFLD
- Post-prandial analysis of fluctuations in the platelet count and platelet function in patients with the familial chylomicronemia syndrome
- Preclinical Development and Characterization of Novel Adeno-Associated Viral Vectors for the Treatment of Lipoprotein Lipase Deficiency
- Qualitative development of the PROMIS Profile v1.0-Familial Chylomicronemia Syndrome (FCS) 28
- Role of lipoprotein lipase activity measurement in the diagnosis of familial chylomicronemia syndrome
- Screening program for familial hyperchylomicronemia syndrome detection: Experience of a university health system
- Severe Hypertriglyceridemia in Patients with Type 2 Diabetes Mellitus Participating in the AMD Annals Initiative
- Severe hypertriglyceridemia: Existing and emerging therapies
- Symptoms and impacts of familial chylomicronemia syndrome: a qualitative study of the patient experience
- The advantages and pitfalls of genetic analysis in the diagnosis and management of lipid disorders
- The longitudinal triglyceride phenotype in heterozygotes with LPL pathogenic variants
- Validation of the familial chylomicronaemia syndrome (FCS) score in an ethnically diverse cohort from UK FCS registry: Implications for diagnosis and differentiation from multifactorial chylomicronaemia syndrome (MCS)
- Variability of longitudinal triglyceride phenotype in patients heterozygous for pathogenic APOA5 variants
- Volanesorsen and triglyceride levels in familial chylomicronemia syndrome: Long-term efficacy and safety data from patients in an open-label extension trial