Familial Chylomicronemia Syndrome
Author:
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1525-1470.2007.00415.x/fullpdf
Reference5 articles.
1. Familial lipoprotein lipase deficiency in infancy: Clinical, biochemical, and molecular study
2. Apolipoprotein C-II deficiency syndrome. Clinical features, lipoprotein characterization, lipase activity, and correction of hypertriglyceridemia after apolipoprotein C-II administration in two affected patients.
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1. Plasma exchange therapy for familial chylomicronemia syndrome in infant: A case report;Medicine;2022-08-12
2. Causes, clinical findings and therapeutic options in chylomicronemia syndrome, a special form of hypertriglyceridemia;Lipids in Health and Disease;2022-02-10
3. Volanesorsen for treatment of familial chylomicronemia syndrome;Expert Review of Cardiovascular Therapy;2021-07-27
4. Lipoprotein and Lipid Metabolism;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2021
5. Estimating health state utilities associated with a rare disease: familial chylomicronemia syndrome (FCS);Journal of Medical Economics;2020-07-01
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