Role of lipoprotein lipase activity measurement in the diagnosis of familial chylomicronemia syndrome

Author:

Rioja José,Ariza María JoséORCID,Benítez-Toledo María José,Espíldora-Hernández JavierORCID,Coca-Prieto Inmaculada,Arrobas-Velilla Teresa,Camacho Ana,Olivecrona Gunilla,Sánchez-Chaparro Miguel Ángel,Valdivielso PedroORCID

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference32 articles.

1. Differences between familial chylomicronemia syndrome and multifactorial chylomicronemia;Paquette;Atherosclerosis,2019

2. The familial chylomicronemia syndrome;Santamarina-Fojo;Endocrinol Metab Clin North Am,1998

3. Familial Chylomicronemia (Type I Hyperlipoproteinemia) Due to a Single Missense Mutation in the Lipoprotein Lipase Gene;Ameis,1991

4. Familial chylomicronemia syndrome: an under-recognized cause of severe hypertriglyceridaemia;Baass;J Intern Med,2020

5. Arteriosclerosis, thrombosis, and vascular biology ATVB NAMED LECTURE REVIEW 2019 george lyman duff memorial lecture three decades of examining DNA in patients with dyslipidemia;Hegele;Arterioscler Thromb Vasc Biol,2020

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