Kuivenhoven JA - Search Results

1

Genetic variant of the scavenger receptor BI in humans.

Vergeer M, Korporaal SJ, Franssen R, Meurs I, Out R, Hovingh GK, Hoekstra M, Sierts JA, Dallinga-Thie GM, Motazacker MM, Holleboom AG, Van Berkel TJ, Kastelein JJ, Van Eck M, Kuivenhoven JA. Vergeer M, et al. Among authors: kuivenhoven ja. N Engl J Med. 2011 Jan 13;364(2):136-45. doi: 10.1056/NEJMoa0907687. N Engl J Med. 2011. PMID: 21226579 Free article.

2

Familial high-density-lipoprotein deficiency causing corneal opacities (fish eye disease) in a family of Dutch descent.

Kastelein JJ, Pritchard PH, Erkelens DW, Kuivenhoven JA, Albers JJ, Frohlich JJ. Kastelein JJ, et al. Among authors: kuivenhoven ja. J Intern Med. 1992 Apr;231(4):413-9. doi: 10.1111/j.1365-2796.1992.tb00953.x. J Intern Med. 1992. PMID: 1588268

3

Two novel molecular defects in the LCAT gene are associated with fish eye disease.

Kuivenhoven JA, Stalenhoef AF, Hill JS, Demacker PN, Errami A, Kastelein JJ, Pritchard PH. Kuivenhoven JA, et al. Arterioscler Thromb Vasc Biol. 1996 Feb;16(2):294-303. doi: 10.1161/01.atv.16.2.294. Arterioscler Thromb Vasc Biol. 1996. PMID: 8620346 Free article. Review.

4

A unique genetic and biochemical presentation of fish-eye disease.

Kuivenhoven JA, van Voorst tot Voorst EJ, Wiebusch H, Marcovina SM, Funke H, Assmann G, Pritchard PH, Kastelein JJ. Kuivenhoven JA, et al. J Clin Invest. 1995 Dec;96(6):2783-91. doi: 10.1172/JCI118348. J Clin Invest. 1995. PMID: 8675648 Free PMC article.

5

An intronic mutation in a lariat branchpoint sequence is a direct cause of an inherited human disorder (fish-eye disease).

Kuivenhoven JA, Weibusch H, Pritchard PH, Funke H, Benne R, Assmann G, Kastelein JJ. Kuivenhoven JA, et al. J Clin Invest. 1996 Jul 15;98(2):358-64. doi: 10.1172/JCI118800. J Clin Invest. 1996. PMID: 8755645 Free PMC article.

6

Heterogeneity at the CETP gene locus. Influence on plasma CETP concentrations and HDL cholesterol levels.

Kuivenhoven JA, de Knijff P, Boer JM, Smalheer HA, Botma GJ, Seidell JC, Kastelein JJ, Pritchard PH. Kuivenhoven JA, et al. Arterioscler Thromb Vasc Biol. 1997 Mar;17(3):560-8. doi: 10.1161/01.atv.17.3.560. Arterioscler Thromb Vasc Biol. 1997. PMID: 9102177

7

Ser447stop mutation in lipoprotein lipase is associated with elevated HDL cholesterol levels in normolipidemic males.

Kuivenhoven JA, Groenemeyer BE, Boer JM, Reymer PW, Berghuis R, Bruin T, Jansen H, Seidell JC, Kastelein JJ. Kuivenhoven JA, et al. Arterioscler Thromb Vasc Biol. 1997 Mar;17(3):595-9. doi: 10.1161/01.atv.17.3.595. Arterioscler Thromb Vasc Biol. 1997. PMID: 9102182

8

The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes.

Kuivenhoven JA, Pritchard H, Hill J, Frohlich J, Assmann G, Kastelein J. Kuivenhoven JA, et al. J Lipid Res. 1997 Feb;38(2):191-205. J Lipid Res. 1997. PMID: 9162740 Free article. Review.

9

Genetic variant showing a positive interaction with beta-blocking agents with a beneficial influence on lipoprotein lipase activity, HDL cholesterol, and triglyceride levels in coronary artery disease patients. The Ser447-stop substitution in the lipoprotein lipase gene. REGRESS Study Group.

Groenemeijer BE, Hallman MD, Reymer PW, Gagné E, Kuivenhoven JA, Bruin T, Jansen H, Lie KI, Bruschke AV, Boerwinkle E, Hayden MR, Kastelein JJ. Groenemeijer BE, et al. Among authors: kuivenhoven ja. Circulation. 1997 Jun 17;95(12):2628-35. doi: 10.1161/01.cir.95.12.2628. Circulation. 1997. PMID: 9193431 Clinical Trial.

10

The role of a common variant of the cholesteryl ester transfer protein gene in the progression of coronary atherosclerosis. The Regression Growth Evaluation Statin Study Group.

Kuivenhoven JA, Jukema JW, Zwinderman AH, de Knijff P, McPherson R, Bruschke AV, Lie KI, Kastelein JJ. Kuivenhoven JA, et al. N Engl J Med. 1998 Jan 8;338(2):86-93. doi: 10.1056/NEJM199801083380203. N Engl J Med. 1998. PMID: 9420339 Free article. Clinical Trial.

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