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Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronine.
Jansen J, Friesema EC, Kester MH, Milici C, Reeser M, Grüters A, Barrett TG, Mancilla EE, Svensson J, Wemeau JL, Busi da Silva Canalli MH, Lundgren J, McEntagart ME, Hopper N, Arts WF, Visser TJ. Jansen J, et al. Among authors: arts wf. J Clin Endocrinol Metab. 2007 Jun;92(6):2378-81. doi: 10.1210/jc.2006-2570. Epub 2007 Mar 13. J Clin Endocrinol Metab. 2007. PMID: 17356046
Absence epilepsy and periventricular nodular heterotopia.
de Wit MC, Schippers HM, de Coo IF, Arts WF, Lequin MH, Brooks A, Visser GH, Mancini GM. de Wit MC, et al. Among authors: arts wf. Seizure. 2010 Sep;19(7):450-2. doi: 10.1016/j.seizure.2010.06.013. Epub 2010 Jul 15. Seizure. 2010. PMID: 20637656 Free article.
Clinical and genetic heterogeneity in benign hereditary chorea.
Breedveld GJ, Percy AK, MacDonald ME, de Vries BB, Yapijakis C, Dure LS, Ippel EF, Sandkuijl LA, Heutink P, Arts WF. Breedveld GJ, et al. Among authors: arts wf. Neurology. 2002 Aug 27;59(4):579-84. doi: 10.1212/wnl.59.4.579. Neurology. 2002. PMID: 12196653
PRPS1 mutations: four distinct syndromes and potential treatment.
de Brouwer AP, van Bokhoven H, Nabuurs SB, Arts WF, Christodoulou J, Duley J. de Brouwer AP, et al. Among authors: arts wf. Am J Hum Genet. 2010 Apr 9;86(4):506-18. doi: 10.1016/j.ajhg.2010.02.024. Am J Hum Genet. 2010. PMID: 20380929 Free PMC article. Review.
126 results