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Items: 1 to 20 of 138

1.

Carriers of lecithin cholesterol acyltransferase gene mutations have accelerated atherogenesis as assessed by carotid 3.0-T magnetic resonance imaging [corrected].

Duivenvoorden R, Holleboom AG, van den Bogaard B, Nederveen AJ, de Groot E, Hutten BA, Schimmel AW, Hovingh GK, Kastelein JJ, Kuivenhoven JA, Stroes ES.

J Am Coll Cardiol. 2011 Dec 6;58(24):2481-7. doi: 10.1016/j.jacc.2010.11.092. Erratum in: J Am Coll Cardiol. 2012 Jan 10;59(2):196.

2.

Patients with low HDL-cholesterol caused by mutations in LCAT have increased arterial stiffness.

van den Bogaard B, Holleboom AG, Duivenvoorden R, Hutten BA, Kastelein JJ, Hovingh GK, Kuivenhoven JA, Stroes ES, van den Born BJ.

Atherosclerosis. 2012 Dec;225(2):481-5. doi: 10.1016/j.atherosclerosis.2012.09.022. Epub 2012 Sep 27.

3.

Functional lecithin: cholesterol acyltransferase is not required for efficient atheroprotection in humans.

Calabresi L, Baldassarre D, Castelnuovo S, Conca P, Bocchi L, Candini C, Frigerio B, Amato M, Sirtori CR, Alessandrini P, Arca M, Boscutti G, Cattin L, Gesualdo L, Sampietro T, Vaudo G, Veglia F, Calandra S, Franceschini G.

Circulation. 2009 Aug 18;120(7):628-35. doi: 10.1161/CIRCULATIONAHA.108.818143.

4.

Compromised LCAT function is associated with increased atherosclerosis.

Hovingh GK, Hutten BA, Holleboom AG, Petersen W, Rol P, Stalenhoef A, Zwinderman AH, de Groot E, Kastelein JJ, Kuivenhoven JA.

Circulation. 2005 Aug 9;112(6):879-84. Epub 2005 Aug 1.

5.

Low levels of high-density lipoprotein cholesterol due to lecithin:cholesterol acyltransferase mutations increase carotid atherosclerosis.

Fazio S, Linton MF.

J Am Coll Cardiol. 2011 Dec 6;58(24):2488-90. doi: 10.1016/j.jacc.2010.11.091. No abstract available.

6.

[Atherosclerosis in rheumatoid arthritis: the role of high-resolution B mode ultrasound in the measurement of the arterial intima-media thickness].

Carotti M, Salaffi F, Mangiacotti M, Cerioni A, Giuseppetti GM, Grassi W.

Reumatismo. 2007 Jan-Mar;59(1):38-49. Italian.

7.

ABCA1 mutation carriers with low high-density lipoprotein cholesterol are characterized by a larger atherosclerotic burden.

Bochem AE, van Wijk DF, Holleboom AG, Duivenvoorden R, Motazacker MM, Dallinga-Thie GM, de Groot E, Kastelein JJ, Nederveen AJ, Hovingh GK, Stroes ES.

Eur Heart J. 2013 Jan;34(4):286-91. doi: 10.1093/eurheartj/ehs376. Epub 2012 Nov 7.

8.

Lipid oxidation in carriers of lecithin:cholesterol acyltransferase gene mutations.

Holleboom AG, Daniil G, Fu X, Zhang R, Hovingh GK, Schimmel AW, Kastelein JJ, Stroes ES, Witztum JL, Hutten BA, Tsimikas S, Hazen SL, Chroni A, Kuivenhoven JA.

Arterioscler Thromb Vasc Biol. 2012 Dec;32(12):3066-75. doi: 10.1161/ATVBAHA.112.255711. Epub 2012 Sep 27.

9.

Inherited disorders of HDL metabolism and atherosclerosis.

Hovingh GK, de Groot E, van der Steeg W, Boekholdt SM, Hutten BA, Kuivenhoven JA, Kastelein JJ.

Curr Opin Lipidol. 2005 Apr;16(2):139-45. Review.

PMID:
15767853
10.

The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families.

Calabresi L, Pisciotta L, Costantin A, Frigerio I, Eberini I, Alessandrini P, Arca M, Bon GB, Boscutti G, Busnach G, Frascà G, Gesualdo L, Gigante M, Lupattelli G, Montali A, Pizzolitto S, Rabbone I, Rolleri M, Ruotolo G, Sampietro T, Sessa A, Vaudo G, Cantafora A, Veglia F, Calandra S, Bertolini S, Franceschini G.

Arterioscler Thromb Vasc Biol. 2005 Sep;25(9):1972-8. Epub 2005 Jun 30.

11.

Cardiac mass and function, carotid artery intima-media thickness and lipoprotein (a) levels in children and adolescents with type 1 diabetes mellitus of short duration.

Gunczler P, Lanes R, Lopez E, Esaa S, Villarroel O, Revel-Chion R.

J Pediatr Endocrinol Metab. 2002 Feb;15(2):181-6.

PMID:
11874183
12.

Plasma lecithin:cholesterol acyltransferase and carotid intima-media thickness in European individuals at high cardiovascular risk.

Calabresi L, Baldassarre D, Simonelli S, Gomaraschi M, Amato M, Castelnuovo S, Frigerio B, Ravani A, Sansaro D, Kauhanen J, Rauramaa R, de Faire U, Hamsten A, Smit AJ, Mannarino E, Humphries SE, Giral P, Veglia F, Sirtori CR, Franceschini G, Tremoli E.

J Lipid Res. 2011 Aug;52(8):1569-74. doi: 10.1194/jlr.P014977. Epub 2011 May 19.

13.

Insulin-like growth factor-1 deficiency determines increased intima-media thickness at common carotid arteries in adult patients with growth hormone deficiency.

Colao A, Di Somma C, Filippella M, Rota F, Pivonello R, Orio F, Vitale G, Lombardi G.

Clin Endocrinol (Oxf). 2004 Sep;61(3):360-6.

PMID:
15355453
14.

Plasma lecithin: cholesterol acyltransferase activity is elevated in metabolic syndrome and is an independent marker of increased carotid artery intima media thickness.

Dullaart RP, Perton F, Sluiter WJ, de Vries R, van Tol A.

J Clin Endocrinol Metab. 2008 Dec;93(12):4860-6. doi: 10.1210/jc.2008-1213. Epub 2008 Sep 9.

PMID:
18782872
15.

Cardiovascular status of carriers of the apolipoprotein A-I(Milano) mutant: the Limone sul Garda study.

Sirtori CR, Calabresi L, Franceschini G, Baldassarre D, Amato M, Johansson J, Salvetti M, Monteduro C, Zulli R, Muiesan ML, Agabiti-Rosei E.

Circulation. 2001 Apr 17;103(15):1949-54.

16.

Overexpression of lecithin:cholesterol acyltransferase in transgenic rabbits prevents diet-induced atherosclerosis.

Hoeg JM, Santamarina-Fojo S, Bérard AM, Cornhill JF, Herderick EE, Feldman SH, Haudenschild CC, Vaisman BL, Hoyt RF Jr, Demosky SJ Jr, Kauffman RD, Hazel CM, Marcovina SM, Brewer HB Jr.

Proc Natl Acad Sci U S A. 1996 Oct 15;93(21):11448-53.

18.

Carotid intima-media thickness and plaque in patients with familial hypercholesterolaemia mutations and control subjects.

Tonstad S, Joakimsen O, Stensland-Bugge E, Ose L, Bønaa KH, Leren TP.

Eur J Clin Invest. 1998 Dec;28(12):971-9.

PMID:
9893006
19.

Increased arterial intima-media thickness by B-M mode echodoppler ultrasonography in acromegaly.

Colao A, Spiezia S, Cerbone G, Pivonello R, Marzullo P, Ferone D, Di Somma C, Assanti AP, Lombardi G.

Clin Endocrinol (Oxf). 2001 Apr;54(4):515-24.

PMID:
11318788
20.

High prevalence of mutations in LCAT in patients with low HDL cholesterol levels in The Netherlands: identification and characterization of eight novel mutations.

Holleboom AG, Kuivenhoven JA, Peelman F, Schimmel AW, Peter J, Defesche JC, Kastelein JJ, Hovingh GK, Stroes ES, Motazacker MM.

Hum Mutat. 2011 Nov;32(11):1290-8. doi: 10.1002/humu.21578. Epub 2011 Sep 23.

PMID:
21901787
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