Defesche J - Search Results

1

Integrated guidance on the care of familial hypercholesterolaemia from the International FH Foundation.

Watts GF, Gidding S, Wierzbicki AS, Toth PP, Alonso R, Brown WV, Bruckert E, Defesche J, Lin KK, Livingston M, Mata P, Parhofer KG, Raal FJ, Santos RD, Sijbrands EJ, Simpson WG, Sullivan DR, Susekov AV, Tomlinson B, Wiegman A, Yamashita S, Kastelein JJ; International Familial Hypercholesterolemia Foundation. Watts GF, et al. Among authors: defesche j. Eur J Prev Cardiol. 2015 Jul;22(7):849-54. doi: 10.1177/2047487314533218. Epub 2014 Apr 28. Eur J Prev Cardiol. 2015. PMID: 24776375 Review.

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

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.

10

Differences in the phenotype between children with familial defective apolipoprotein B-100 and familial hypercholesterolemia.

Pimstone SN, Defesche JC, Clee SM, Bakker HD, Hayden MR, Kastelein JJ. Pimstone SN, et al. Among authors: defesche jc. Arterioscler Thromb Vasc Biol. 1997 May;17(5):826-33. doi: 10.1161/01.atv.17.5.826. Arterioscler Thromb Vasc Biol. 1997. PMID: 9157944

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