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)-Reference-Cited by-同舟云学术

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)

Published:2024-04 Issue: Volume:391 Page:117476
ISSN:0021-9150
Container-title:Atherosclerosis
language:en
Short-container-title:Atherosclerosis

Author:

Bashir Bilal,Kwok See,Wierzbicki Anthony S.,Jones Alan,Dawson Charlotte,Downie Paul,Jenkinson Fiona,Delaney Hannah,Mansfield Michael,Datta Dev,Teoh Yee,Hamilton Paul,Forrester Natalie,O'Sullivan Dawn,Ferdousi Maryam,Durrington Paul N.,AbdelRazik Alaa,Gallo Antonio,Moulin Philippe,Soran Handrean^ORCID

Funder

Chiesi Pharmaceuticals

Publisher

Elsevier BV

Reference18 articles.

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2. Severe hypertriglyceridaemia and chylomicronaemia syndrome—causes, clinical presentation, and therapeutic options;Bashir;Metabolites,2023

3. Clinical and biochemical features of different molecular etiologies of familial chylomicronemia;Hegele;J Clin Lipidol,2018

4. Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): expert panel recommendations and proposal of an “FCS score”;Moulin;Atherosclerosis,2018

5. The polygenic nature of hypertriglyceridaemia: implications for definition, diagnosis, and management;Hegele;Lancet Diabetes Endocrinol.,2014

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1. Pancreatic and cardiometabolic complications of severe hypertriglyceridaemia;Current Opinion in Lipidology;2024-06-06