Defesche JC - Search Results

1

Advances in genetics show the need for extending screening strategies for autosomal dominant hypercholesterolaemia.

Motazacker MM, Pirruccello J, Huijgen R, Do R, Gabriel S, Peter J, Kuivenhoven JA, Defesche JC, Kastelein JJ, Hovingh GK, Zelcer N, Kathiresan S, Fouchier SW. Motazacker MM, et al. Among authors: defesche jc. Eur Heart J. 2012 Jun;33(11):1360-6. doi: 10.1093/eurheartj/ehs010. Epub 2012 Mar 8. Eur Heart J. 2012. PMID: 22408029

2

Detection of the Pro664-Leu mutation in the low-density lipoprotein receptor and its relation to lipoprotein(a) levels in patients with familial hypercholesterolemia of Dutch ancestry from The Netherlands and Canada.

Defesche JC, van de Ree MA, Kastelein JJ, van Diermen DE, Janssens NW, van Doormaal JJ, Hayden MR. Defesche JC, et al. Clin Genet. 1992 Dec;42(6):273-80. Clin Genet. 1992. PMID: 1493640

3

[The treatment of familial hypercholesterolemia].

Lansberg PJ, Kastelein JJ, Defesche JC, ten Cate JW. Lansberg PJ, et al. Among authors: defesche jc. Ned Tijdschr Geneeskd. 1992 Apr 11;136(15):734-8. Ned Tijdschr Geneeskd. 1992. PMID: 1560866 Review. Dutch. No abstract available.

4

South African founder mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia in the Dutch population.

Defesche JC, van Diermen DE, Lansberg PJ, Lamping RJ, Reymer PW, Hayden MR, Kastelein JJ. Defesche JC, et al. Hum Genet. 1993 Dec;92(6):567-70. doi: 10.1007/BF00420940. Hum Genet. 1993. PMID: 7903269

5

Decreased resistance against in vitro oxidation of LDL from patients with familial defective apolipoprotein B-100.

Stalenhoef AF, Defesche JC, Kleinveld HA, Demacker PN, Kastelein JJ. Stalenhoef AF, et al. Among authors: defesche jc. Arterioscler Thromb. 1994 Mar;14(3):489-93. doi: 10.1161/01.atv.14.3.489. Arterioscler Thromb. 1994. PMID: 8123657

6

Screening for familial defective apolipoprotein B-100 with improved U937 monocyte proliferation assay.

Van den Broek AJ, Hollaar L, Schaefer HI, Van der Laarse A, Schuster H, Defesche JC, Kastelein JJ, Van 't Hooft FM. Van den Broek AJ, et al. Among authors: defesche jc. Clin Chem. 1994 Mar;40(3):395-9. Clin Chem. 1994. PMID: 8131274

7

Familial defective apolipoprotein B-100 is clinically indistinguishable from familial hypercholesterolemia.

Defesche JC, Pricker KL, Hayden MR, van der Ende BE, Kastelein JJ. Defesche JC, et al. Arch Intern Med. 1993 Oct 25;153(20):2349-56. Arch Intern Med. 1993. PMID: 8215738

8

Analysis of the Afrikaner mutation in exon 9 of the low-density lipoprotein receptor gene in a large Dutch kindred suffering from familial hypercholesterolaemia.

Defesche JC, Lansberg PJ, Reymer PW, Lamping RJ, Kastelein JJ. Defesche JC, et al. Neth J Med. 1993 Feb;42(1-2):53-60. Neth J Med. 1993. PMID: 8446226

9

Identification of a double mutation in the low-density lipoprotein receptor gene causing familial hypercholesterolemia.

Lombardi P, Kamerling SW, Defesche JC, Kastelein JJ, Havekes LM. Lombardi P, et al. Among authors: defesche jc. Clin Genet. 1996 Dec;50(6):525-6. doi: 10.1111/j.1399-0004.1996.tb02727.x. Clin Genet. 1996. PMID: 9147888 No abstract available.

10

Sib-pair analysis detects elevated Lp(a) levels and large variation of Lp(a) concentration in subjects with familial defective ApoB.

van der Hoek YY, Lingenhel A, Kraft HG, Defesche JC, Kastelein JJ, Utermann G. van der Hoek YY, et al. Among authors: defesche jc. J Clin Invest. 1997 May 1;99(9):2269-73. doi: 10.1172/JCI119402. J Clin Invest. 1997. PMID: 9151801 Free PMC article.

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