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Journal Abstract Search

346 related items for PubMed ID: 29748187

  • 1. 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 04; 138(10):1000-1007. PubMed ID: 29748187
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  • 2. Lipoprotein subfractions highly associated with renal damage in familial lecithin:cholesterol acyltransferase deficiency.
    Kuroda M, Holleboom AG, Stroes ES, Asada S, Aoyagi Y, Kamata K, Yamashita S, Ishibashi S, Saito Y, Bujo H.
    Arterioscler Thromb Vasc Biol; 2014 Aug 04; 34(8):1756-62. PubMed ID: 24876348
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  • 3. 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 04; 207(2):452-7. PubMed ID: 19515369
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  • 9. 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 04; 187(1):101-9. PubMed ID: 16216249
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  • 12. 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 Jul 04; 8(2):223-30. PubMed ID: 24636183
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  • 13. Proteinuria in early childhood due to familial LCAT deficiency caused by loss of a disulfide bond in lecithin:cholesterol acyl transferase.
    Holleboom AG, Kuivenhoven JA, van Olden CC, Peter J, Schimmel AW, Levels JH, Valentijn RM, Vos P, Defesche JC, Kastelein JJ, Hovingh GK, Stroes ES, Hollak CE.
    Atherosclerosis; 2011 May 04; 216(1):161-5. PubMed ID: 21315357
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  • 14. Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemia.
    Conca P, Pileggi S, Simonelli S, Boer E, Boscutti G, Magnolo L, Tarugi P, Penco S, Franceschini G, Calabresi L, Gomaraschi M.
    J Clin Lipidol; 2012 May 04; 6(3):244-50. PubMed ID: 22658148
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  • 15. Genetic lecithin:cholesterol acyltransferase deficiency and cardiovascular disease.
    Calabresi L, Simonelli S, Gomaraschi M, Franceschini G.
    Atherosclerosis; 2012 Jun 04; 222(2):299-306. PubMed ID: 22189200
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  • 18. A systematic review of the natural history and biomarkers of primary lecithin:cholesterol acyltransferase deficiency.
    Vitali C, Bajaj A, Nguyen C, Schnall J, Chen J, Stylianou K, Rader DJ, Cuchel M.
    J Lipid Res; 2022 Mar 04; 63(3):100169. PubMed ID: 35065092
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  • 20. 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 04; 36(5):967-74. PubMed ID: 7658168
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