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A negative iodine balance is found in healthy neonates compared with neonates with thyroid agenesis.
J Endocrinol. 1999 Apr;161(1):115-20. doi: 10.1677/joe.0.1610115.
J Endocrinol. 1999.
PMID: 10194535
The quantity of thyroid hormone in human milk is too low to influence plasma thyroid hormone levels in the very preterm infant.
van Wassenaer AG, Stulp MR, Valianpour F, Tamminga P, Ris Stalpers C, de Randamie JS, van Beusekom C, de Vijlder JJ.
van Wassenaer AG, et al. Among authors: de randamie js.
Clin Endocrinol (Oxf). 2002 May;56(5):621-7. doi: 10.1046/j.1365-2265.2002.01526.x.
Clin Endocrinol (Oxf). 2002.
PMID: 12030913
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Two decades of screening for congenital hypothyroidism in The Netherlands: TPO gene mutations in total iodide organification defects (an update).
Bakker B, Bikker H, Vulsma T, de Randamie JS, Wiedijk BM, De Vijlder JJ.
Bakker B, et al. Among authors: de randamie js.
J Clin Endocrinol Metab. 2000 Oct;85(10):3708-12. doi: 10.1210/jcem.85.10.6878.
J Clin Endocrinol Metab. 2000.
PMID: 11061528
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Molecular characterization of iodotyrosine dehalogenase deficiency in patients with hypothyroidism.
Afink G, Kulik W, Overmars H, de Randamie J, Veenboer T, van Cruchten A, Craen M, Ris-Stalpers C.
Afink G, et al. Among authors: de randamie j.
J Clin Endocrinol Metab. 2008 Dec;93(12):4894-901. doi: 10.1210/jc.2008-0865. Epub 2008 Sep 2.
J Clin Endocrinol Metab. 2008.
PMID: 18765512
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Initial characterization of C16orf89, a novel thyroid-specific gene.
Afink GB, Veenboer G, de Randamie J, Keijser R, Meischl C, Niessen H, Ris-Stalpers C.
Afink GB, et al. Among authors: de randamie j.
Thyroid. 2010 Jul;20(7):811-21. doi: 10.1089/thy.2009.0366.
Thyroid. 2010.
PMID: 20578903
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Sequencing for LIPA mutations in patients with a clinical diagnosis of familial hypercholesterolemia.
Sjouke B, Defesche JC, de Randamie JSE, Wiegman A, Fouchier SW, Hovingh GK.
Sjouke B, et al. Among authors: de randamie jse.
Atherosclerosis. 2016 Aug;251:263-265. doi: 10.1016/j.atherosclerosis.2016.07.008. Epub 2016 Jul 9.
Atherosclerosis. 2016.
PMID: 27423329
Free article.
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Genetic variation in APOB, PCSK9, and ANGPTL3 in carriers of pathogenic autosomal dominant hypercholesterolemic mutations with unexpected low LDL-Cl Levels.
Huijgen R, Sjouke B, Vis K, de Randamie JS, Defesche JC, Kastelein JJ, Hovingh GK, Fouchier SW.
Huijgen R, et al. Among authors: de randamie js.
Hum Mutat. 2012 Feb;33(2):448-55. doi: 10.1002/humu.21660. Epub 2011 Dec 22.
Hum Mutat. 2012.
PMID: 22095935
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