Arts WF - Search Results

1

Hereditary porencephaly: clinical and MRI findings in two Dutch families.

Mancini GM, de Coo IF, Lequin MH, Arts WF. Mancini GM, et al. Among authors: arts wf. Eur J Paediatr Neurol. 2004;8(1):45-54. doi: 10.1016/j.ejpn.2003.10.002. Eur J Paediatr Neurol. 2004. PMID: 15023374

2

Long-term follow-up of type 1 lissencephaly: survival is related to neuroimaging abnormalities.

de Wit MC, de Rijk-van Andel J, Halley DJ, Poddighe PJ, Arts WF, de Coo IF, Mancini GM. de Wit MC, et al. Among authors: arts wf. Dev Med Child Neurol. 2011 May;53(5):417-21. doi: 10.1111/j.1469-8749.2011.03937.x. Epub 2011 Mar 17. Dev Med Child Neurol. 2011. PMID: 21410694 Free article.

3

Benign familial infantile convulsions: a clinical study of seven Dutch families.

Callenbach PM, de Coo RF, Vein AA, Arts WF, Oosterwijk J, Hageman G, ten Houten R, Terwindt GM, Lindhout D, Frants RR, Brouwer OF. Callenbach PM, et al. Among authors: arts wf. Eur J Paediatr Neurol. 2002;6(5):269-83. doi: 10.1053/ejpn.2002.0609. Eur J Paediatr Neurol. 2002. PMID: 12374579 Free article.

4

Effect of simvastatin on cognitive functioning in children with neurofibromatosis type 1: a randomized controlled trial.

Krab LC, de Goede-Bolder A, Aarsen FK, Pluijm SM, Bouman MJ, van der Geest JN, Lequin M, Catsman CE, Arts WF, Kushner SA, Silva AJ, de Zeeuw CI, Moll HA, Elgersma Y. Krab LC, et al. Among authors: arts wf. JAMA. 2008 Jul 16;300(3):287-94. doi: 10.1001/jama.300.3.287. JAMA. 2008. PMID: 18632543 Free PMC article. Clinical Trial.

5

Frequent fever episodes and the risk of febrile seizures: the Generation R study.

Visser AM, Jaddoe VW, Breteler MM, Hofman A, Moll HA, Arts WF. Visser AM, et al. Among authors: arts wf. Eur J Paediatr Neurol. 2012 Jan;16(1):29-34. doi: 10.1016/j.ejpn.2011.09.007. Epub 2011 Oct 2. Eur J Paediatr Neurol. 2012. PMID: 21968332

6

Add-on levetiracetam in children and adolescents with refractory epilepsy: results of an open-label multi-centre study.

Callenbach PM, Arts WF, ten Houten R, Augustijn P, Gunning WB, Peeters EA, Weber AM, Stroink H, Geerts Y, Geerts AT, Brouwer OF. Callenbach PM, et al. Among authors: arts wf. Eur J Paediatr Neurol. 2008 Jul;12(4):321-7. doi: 10.1016/j.ejpn.2007.09.004. Epub 2007 Oct 18. Eur J Paediatr Neurol. 2008. PMID: 17950011 Clinical Trial.

7

Mutations in TITF-1 are associated with benign hereditary chorea.

Breedveld GJ, van Dongen JW, Danesino C, Guala A, Percy AK, Dure LS, Harper P, Lazarou LP, van der Linde H, Joosse M, Grüters A, MacDonald ME, de Vries BB, Arts WF, Oostra BA, Krude H, Heutink P. Breedveld GJ, et al. Among authors: arts wf. Hum Mol Genet. 2002 Apr 15;11(8):971-9. doi: 10.1093/hmg/11.8.971. Hum Mol Genet. 2002. PMID: 11971878

8

Impact of neurofibromatosis type 1 on school performance.

Krab LC, Aarsen FK, de Goede-Bolder A, Catsman-Berrevoets CE, Arts WF, Moll HA, Elgersma Y. Krab LC, et al. Among authors: arts wf. J Child Neurol. 2008 Sep;23(9):1002-10. doi: 10.1177/0883073808316366. J Child Neurol. 2008. PMID: 18827266

9

Identification, functional analysis, prevalence and treatment of monocarboxylate transporter 8 (MCT8) mutations in a cohort of adult patients with mental retardation.

Visser WE, Vrijmoeth P, Visser FE, Arts WF, van Toor H, Visser TJ. Visser WE, et al. Among authors: arts wf. Clin Endocrinol (Oxf). 2013 Feb;78(2):310-5. doi: 10.1111/cen.12023. Clin Endocrinol (Oxf). 2013. PMID: 22924588

10

Characterisation of TSC1 promoter deletions in tuberous sclerosis complex patients.

van den Ouweland AM, Elfferich P, Zonnenberg BA, Arts WF, Kleefstra T, Nellist MD, Millan JM, Withagen-Hermans C, Maat-Kievit AJ, Halley DJ. van den Ouweland AM, et al. Among authors: arts wf. Eur J Hum Genet. 2011 Feb;19(2):157-63. doi: 10.1038/ejhg.2010.156. Epub 2010 Sep 29. Eur J Hum Genet. 2011. PMID: 20877415 Free PMC article.

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