The P274S Mutation of Lecithin-Cholesterol Acyltransferase (LCAT) and Its Clinical Manifestations in a Large Kindred-Reference-Cited by-同舟云学术

The P274S Mutation of Lecithin-Cholesterol Acyltransferase (LCAT) and Its Clinical Manifestations in a Large Kindred

Published:2019-10 Issue:4 Volume:74 Page:510-522
ISSN:0272-6386
Container-title:American Journal of Kidney Diseases
language:en
Short-container-title:American Journal of Kidney Diseases

Author:

Fountoulakis Nikolaos,Lioudaki Eirini,Lygerou Dimitra,Dermitzaki Eleftheria-Kleio,Papakitsou Ioanna,Kounali Vasiliki,Holleboom Adriaan G.,Stratigis Spyros,Belogianni Christina,Syngelaki Paraskevi,Stratakis Stavros,Evangeliou Athanasios,Gakiopoulou Hariklia,Kuivenhoven Jan Albert,Wevers Ron,Dafnis Eugene,Stylianou Kostas

Publisher

Elsevier BV

Subject

Nephrology

Reference47 articles.

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4. Atherogenic impact of lecithin-cholesterol acyltransferase and its relation to cholesterol esterification rate in HDL (FER(HDL)) and AIP [log(TG/HDL-C)] biomarkers: the butterfly effect?;Dobiášová;Physiol Res,2017

5. A study of the small spherical high density lipoproteins of patients afflicted with familial lecithin: cholesterol acyltransferase deficiency;Chen;J Lipid Res,1984

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3. Novel therapeutic opportunities for familial lecithin:cholesterol acyltransferase deficiency: promises and challenges;Current Opinion in Lipidology;2022-12-06

4. A systematic review of the natural history and biomarkers of primary lecithin:cholesterol acyltransferase deficiency;Journal of Lipid Research;2022-03

5. The HDL mimetic CER‐001 remodels plasma lipoproteins and reduces kidney lipid deposits in inherited lecithin:cholesterol acyltransferase deficiency;Journal of Internal Medicine;2021-11-11