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familial lecithin cholesterol acyltransferase deficiency相关文献:
Lecithin-Cholesterol Acyltransferase Deficiency.
Carty JR, Anastasopoulou C.
2024 Feb 24. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–.
PMID:38753926
Novel therapeutic opportunities for familial lecithin:cholesterol acyltransferase deficiency: promises and challenges.
Vitali C, Rader DJ, Cuchel M.
Curr Opin Lipidol. 2023 Apr 1;34(2):35-43. doi: 10.1097/MOL.0000000000000864. Epub 2022 Dec 6.
PMID:36473023
Familial lecithin-cholesterol acyltransferase deficiency: If so rare, why so frequent in the state of Piaui, northeastern Brazil?
de Serpa Brandão RMS, Britto FB, do Monte Neto JT, Lima MC, do Monte SJH, de Sousa Lima AV, Pereira EM, da Silva HJN, Oliveira DMTE, Coelho AGB, da Silva AS.
Mol Genet Metab Rep. 2022 Jan 3;30:100840. doi: 10.1016/j.ymgmr.2021.100840. eCollection 2022 Mar.
PMID:35242572
Familial lecithin:cholesterol acyltransferase deficiency: First-in-human treatment with enzyme replacement.
Shamburek RD, Bakker-Arkema R, Auerbach BJ, Krause BR, Homan R, Amar MJ, Freeman LA, Remaley AT.
J Clin Lipidol. 2016 Mar-Apr;10(2):356-67. doi: 10.1016/j.jacl.2015.12.007. Epub 2015 Dec 23.
PMID:27055967
Familial lecithin: cholesterol acyltransferase (LCAT) deficiency. An updated review Spring 1988.
Gjone E.
Ophthalmic Paediatr Genet. 1988 Nov;9(3):167-9. doi: 10.3109/13816818809031494.
PMID:3068599
The function of lecithin:cholesterol acyltransferase (LCAT).
Norum KR.
Scand J Clin Lab Invest. 2017 Jul;77(4):235-236. doi: 10.1080/00365513.2017.1308008. Epub 2017 Apr 10.
PMID:28394642
A review on lecithin:cholesterol acyltransferase deficiency.
Saeedi R, Li M, Frohlich J.
Clin Biochem. 2015 May;48(7-8):472-5. doi: 10.1016/j.clinbiochem.2014.08.014. Epub 2014 Aug 27.
PMID:25172171
Genetic lecithin:cholesterol acyltransferase deficiency and cardiovascular disease.
Calabresi L, Simonelli S, Gomaraschi M, Franceschini G.
Atherosclerosis. 2012 Jun;222(2):299-306. doi: 10.1016/j.atherosclerosis.2011.11.034. Epub 2011 Nov 28.
PMID:22189200
A case of acquired lecithin:cholesterol acyltransferase deficiency with sarcoidosis that remitted spontaneously.
Akiko T, Okura T, Nagao T, Kukida M, Enomoto D, Miyoshi KI, Higaki J, Kuroda M, Bujo H.
CEN Case Rep. 2016 Nov;5(2):192-196. doi: 10.1007/s13730-016-0223-4. Epub 2016 Jun 7.
PMID:28508975
Two novel variants in the lecithin:cholesterol acyltransferase gene resulted in classic LCAT deficiency.
Fistrek Prlic M, Coric M, Calabresi L, Pavanello C, Mosca L, Cavallari U, Vukovic Brinar I, Karanovic S, Laganovic M, Jelakovic B.
Atheroscler Plus. 2022 Jun 2;49:28-31. doi: 10.1016/j.athplu.2022.05.005. eCollection 2022 Aug.
PMID:36644204
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