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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: wiegman a. 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
Kawasaki disease: a maturational defect in immune responsiveness.
Kuijpers TW, Wiegman A, van Lier RA, Roos MT, Wertheim-van Dillen PM, Pinedo S, Ottenkamp J. Kuijpers TW, et al. Among authors: wiegman a. J Infect Dis. 1999 Dec;180(6):1869-77. doi: 10.1086/315111. J Infect Dis. 1999. PMID: 10558943
The curious case of the orange coloured tonsils.
Ravesloot MJ, Bril H, Braamskamp MJ, Wiegman A, Wong Chung RP. Ravesloot MJ, et al. Among authors: wiegman a. Int J Pediatr Otorhinolaryngol. 2014 Dec;78(12):2305-7. doi: 10.1016/j.ijporl.2014.09.011. Epub 2014 Sep 22. Int J Pediatr Otorhinolaryngol. 2014. PMID: 25441921
[Refusal of medical treatment in an acute comatose patient].
Sijpkens DE, Looten DM, Corté WG, Wiegman A, Speelman P, Romijn JA. Sijpkens DE, et al. Among authors: wiegman a. Ned Tijdschr Geneeskd. 2011;155(47):A3788. Ned Tijdschr Geneeskd. 2011. PMID: 22129809 Dutch.
A boy with autosomal recessive hypercholesterolaemia.
Rodenburg J, Wiegman A, Vissers MN, Kastelein JJ, Stalenhoef AF. Rodenburg J, et al. Among authors: wiegman a. Neth J Med. 2004 Mar;62(3):89-93. Neth J Med. 2004. PMID: 15209474 Free article.
145 results