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9. [LCAT deficiency: a nephrological diagnosis]. Boscutti G; Calabresi L; Pizzolitto S; Boer E; Bosco M; Mattei PL; Martone M; Milutinovic N; Berbecar D; Beltram E; Franceschini G G Ital Nefrol; 2011; 28(4):369-82. PubMed ID: 21809306 [TBL] [Abstract][Full Text] [Related]
10. Compound heterozygosity (G71R/R140H) in the lecithin:cholesterol acyltransferase (LCAT) gene results in an intermediate phenotype between LCAT-deficiency and fish-eye disease. Hörl G; Kroisel PM; Wagner E; Tiran B; Petek E; Steyrer E Atherosclerosis; 2006 Jul; 187(1):101-9. PubMed ID: 16216249 [TBL] [Abstract][Full Text] [Related]
11. LCAT deficiency: a systematic review with the clinical and genetic description of Mexican kindred. Mehta R; Elías-López D; Martagón AJ; Pérez-Méndez OA; Sánchez MLO; Segura Y; Tusié MT; Aguilar-Salinas CA Lipids Health Dis; 2021 Jul; 20(1):70. PubMed ID: 34256778 [TBL] [Abstract][Full Text] [Related]
12. Complete and Partial Lecithin:Cholesterol Acyltransferase Deficiency Is Differentially Associated With Atherosclerosis. Oldoni F; Baldassarre D; Castelnuovo S; Ossoli A; Amato M; van Capelleveen J; Hovingh GK; De Groot E; Bochem A; Simonelli S; Barbieri S; Veglia F; Franceschini G; Kuivenhoven JA; Holleboom AG; Calabresi L Circulation; 2018 Sep; 138(10):1000-1007. PubMed ID: 29748187 [TBL] [Abstract][Full Text] [Related]
13. [Lecithin: cholesterol acyltransferase (LCAT)--the genetic analysis of familial LCAT deficiency and fish eye disease]. Bujo H; Saito Y Nihon Rinsho; 1995 May; 53(5):1260-6. PubMed ID: 7602789 [TBL] [Abstract][Full Text] [Related]
14. A kindred with fish eye disease, corneal opacities, marked high-density lipoprotein deficiency, and statin therapy. Dimick SM; Sallee B; Asztalos BF; Pritchard PH; Frohlich J; Schaefer EJ J Clin Lipidol; 2014; 8(2):223-30. PubMed ID: 24636183 [TBL] [Abstract][Full Text] [Related]
15. Characterization of a new LCAT mutation causing familial LCAT deficiency (FLD) and the role of APOE as a modifier gene of the FLD phenotype. Baass A; Wassef H; Tremblay M; Bernier L; Dufour R; Davignon J Atherosclerosis; 2009 Dec; 207(2):452-7. PubMed ID: 19515369 [TBL] [Abstract][Full Text] [Related]
16. In vitro expression of natural mutants of human lecithin:cholesterol acyltransferase. Qu SJ; Fan HZ; Blanco-Vaca F; Pownall HJ J Lipid Res; 1995 May; 36(5):967-74. PubMed ID: 7658168 [TBL] [Abstract][Full Text] [Related]
17. Lecithin-cholesterol acyltransferase (LCAT) deficiency without mutations in the coding sequence: a case report and literature review. Shoji K; Morita H; Ishigaki Y; Rivard CJ; Takayasu M; Nakayama K; Nakayama T; Inoue Y; Ayaki M; Yoshimura A Clin Nephrol; 2011 Oct; 76(4):323-8. PubMed ID: 21955868 [TBL] [Abstract][Full Text] [Related]
18. LCAT- targeted therapies: Progress, failures and future. Yang K; Wang J; Xiang H; Ding P; Wu T; Ji G Biomed Pharmacother; 2022 Mar; 147():112677. PubMed ID: 35121343 [TBL] [Abstract][Full Text] [Related]
19. Immune-mediated acquired lecithin-cholesterol acyltransferase deficiency: A case report and literature review. Ishibashi R; Takemoto M; Tsurutani Y; Kuroda M; Ogawa M; Wakabayashi H; Uesugi N; Nagata M; Imai N; Hattori A; Sakamoto K; Kitamoto T; Maezawa Y; Narita I; Hiroi S; Furuta A; Miida T; Yokote K J Clin Lipidol; 2018; 12(4):888-897.e2. PubMed ID: 29937398 [TBL] [Abstract][Full Text] [Related]
20. A novel frameshift mutation of the lecithin:cholesterol acyltransferase (LCAT) gene associated with renal failure in familial LCAT deficiency. Bender BU; Quaschning T; Neumann HP; Schmidt D; Kraemer-Guth A Clin Chem Lab Med; 2007; 45(4):483-6. PubMed ID: 17439325 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]