Familial chylomicronemia syndrome due to a heterozygous deletion of the chromosome 8 treated with the apoCIII inhibitor volanesorsen-Reference-Cited by-同舟云学术

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Familial chylomicronemia syndrome due to a heterozygous deletion of the chromosome 8 treated with the apoCIII inhibitor volanesorsen

Published:2021-10-22 Issue:42 Volume:100 Page:e27573
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Tünnemann-Tarr Adrienn,Scharnagl Hubert,Katzmann Julius L.,Stürzebecher Paulina,Laufs Ulrich

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference19 articles.

1. Familial chylomicronemia syndrome: bringing to life dietary recommendations throughout the life span;Williams;J Clin Lipidol,2018

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

3. Clinical review on triglycerides;Laufs;Eur Heart J,2020

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

5. Targeting APOC3 in the familial chylomicronemia syndrome;Gaudet;N Engl J Med,2014

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Bezafibrate/volanesorsen;Reactions Weekly;2022-05

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