Kindt I - Search Results

1

Frequency of pregnancy-related venous thromboembolism in anticoagulant factor-deficient women: implications for prophylaxis.

Friederich PW, Sanson BJ, Simioni P, Zanardi S, Huisman MV, Kindt I, Prandoni P, Büller HR, Girolami A, Prins MH. Friederich PW, et al. Among authors: kindt i. Ann Intern Med. 1996 Dec 15;125(12):955-60. doi: 10.7326/0003-4819-125-12-199612150-00003. Ann Intern Med. 1996. PMID: 8967705

2

Severe heterozygous familial hypercholesterolemia and risk for cardiovascular disease: a study of a cohort of 14,000 mutation carriers.

Besseling J, Kindt I, Hof M, Kastelein JJ, Hutten BA, Hovingh GK. Besseling J, et al. Among authors: kindt i. Atherosclerosis. 2014 Mar;233(1):219-23. doi: 10.1016/j.atherosclerosis.2013.12.020. Epub 2014 Jan 11. Atherosclerosis. 2014. PMID: 24529147 Free article.

3

Perceived risk and representations of cardiovascular disease and preventive behaviour in people diagnosed with familial hypercholesterolemia: a cross-sectional questionnaire study.

Claassen L, Henneman L, Kindt I, Marteau TM, Timmermans DR. Claassen L, et al. Among authors: kindt i. J Health Psychol. 2010 Jan;15(1):33-43. doi: 10.1177/1359105309345170. J Health Psychol. 2010. PMID: 20064882

4

Follow-up of children diagnosed with familial hypercholesterolemia in a national genetic screening program.

Avis HJ, Kusters DM, Vissers MN, Huijgen R, Janssen TH, Wiegman A, Kindt I, Kastelein JJ, Wijburg FA, Hutten BA. Avis HJ, et al. Among authors: kindt i. J Pediatr. 2012 Jul;161(1):99-103. doi: 10.1016/j.jpeds.2011.12.037. Epub 2012 Jan 28. J Pediatr. 2012. PMID: 22284919

5

Discriminative ability of LDL-cholesterol to identify patients with familial hypercholesterolemia: a cross-sectional study in 26,406 individuals tested for genetic FH.

Huijgen R, Hutten BA, Kindt I, Vissers MN, Kastelein JJ. Huijgen R, et al. Among authors: kindt i. Circ Cardiovasc Genet. 2012 Jun;5(3):354-9. doi: 10.1161/CIRCGENETICS.111.962456. Epub 2012 May 2. Circ Cardiovasc Genet. 2012. PMID: 22553281

6

Two years after molecular diagnosis of familial hypercholesterolemia: majority on cholesterol-lowering treatment but a minority reaches treatment goal.

Huijgen R, Kindt I, Verhoeven SB, Sijbrands EJ, Vissers MN, Kastelein JJ, Hutten BA. Huijgen R, et al. Among authors: kindt i. PLoS One. 2010 Feb 15;5(2):e9220. doi: 10.1371/journal.pone.0009220. PLoS One. 2010. PMID: 20169164 Free PMC article.

7

Assessment of carotid atherosclerosis in normocholesterolemic individuals with proven mutations in the low-density lipoprotein receptor or apolipoprotein B genes.

Huijgen R, Vissers MN, Kindt I, Trip MD, de Groot E, Kastelein JJ, Hutten BA. Huijgen R, et al. Among authors: kindt i. Circ Cardiovasc Genet. 2011 Aug 1;4(4):413-7. doi: 10.1161/CIRCGENETICS.110.959239. Epub 2011 Jun 4. Circ Cardiovasc Genet. 2011. PMID: 21642693

8

Homozygous autosomal dominant hypercholesterolaemia in the Netherlands: prevalence, genotype-phenotype relationship, and clinical outcome.

Sjouke B, Kusters DM, Kindt I, Besseling J, Defesche JC, Sijbrands EJ, Roeters van Lennep JE, Stalenhoef AF, Wiegman A, de Graaf J, Fouchier SW, Kastelein JJ, Hovingh GK. Sjouke B, et al. Among authors: kindt i. Eur Heart J. 2015 Mar 1;36(9):560-5. doi: 10.1093/eurheartj/ehu058. Epub 2014 Feb 28. Eur Heart J. 2015. PMID: 24585268

9

Improved access to life insurance after genetic diagnosis of familial hypercholesterolaemia: cross-sectional postal questionnaire study.

Huijgen R, Homsma SJ, Hutten BA, Kindt I, Vissers MN, Kastelein JJ, van Rijckevorsel JL. Huijgen R, et al. Among authors: kindt i. Eur J Hum Genet. 2012 Jul;20(7):722-8. doi: 10.1038/ejhg.2012.5. Epub 2012 Feb 1. Eur J Hum Genet. 2012. PMID: 22293687 Free PMC article.

10

Functionality of sequence variants in the genes coding for the low-density lipoprotein receptor and apolipoprotein B in individuals with inherited hypercholesterolemia.

Huijgen R, Kindt I, Fouchier SW, Defesche JC, Hutten BA, Kastelein JJ, Vissers MN. Huijgen R, et al. Among authors: kindt i. Hum Mutat. 2010 Jun;31(6):752-60. doi: 10.1002/humu.21258. Hum Mutat. 2010. PMID: 20506408

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