Arts WF - Search Results

1

Cognitive deficits and predictors 3 years after diagnosis of a pilocytic astrocytoma in childhood.

Aarsen FK, Paquier PF, Arts WF, Van Veelen ML, Michiels E, Lequin M, Catsman-Berrevoets CE. Aarsen FK, et al. Among authors: arts wf. J Clin Oncol. 2009 Jul 20;27(21):3526-32. doi: 10.1200/JCO.2008.19.6303. Epub 2009 May 11. J Clin Oncol. 2009. PMID: 19433687

2

Cognitive outcome of patients with classic infantile Pompe disease receiving enzyme therapy.

Ebbink BJ, Aarsen FK, van Gelder CM, van den Hout JM, Weisglas-Kuperus N, Jaeken J, Lequin MH, Arts WF, van der Ploeg AT. Ebbink BJ, et al. Among authors: arts wf. Neurology. 2012 May 8;78(19):1512-8. doi: 10.1212/WNL.0b013e3182553c11. Epub 2012 Apr 25. Neurology. 2012. PMID: 22539577

3

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.

4

Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly.

Breedveld G, de Coo IF, Lequin MH, Arts WF, Heutink P, Gould DB, John SW, Oostra B, Mancini GM. Breedveld G, et al. Among authors: arts wf. J Med Genet. 2006 Jun;43(6):490-5. doi: 10.1136/jmg.2005.035584. Epub 2005 Aug 17. J Med Genet. 2006. PMID: 16107487 Free PMC article.

5

Eight years experience with enzyme replacement therapy in two children and one adult with Pompe disease.

van Capelle CI, Winkel LP, Hagemans ML, Shapira SK, Arts WF, van Doorn PA, Hop WC, Reuser AJ, van der Ploeg AT. van Capelle CI, et al. Among authors: arts wf. Neuromuscul Disord. 2008 Jun;18(6):447-52. doi: 10.1016/j.nmd.2008.04.009. Epub 2008 May 27. Neuromuscul Disord. 2008. PMID: 18508267

6

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

7

Effect of enzyme therapy in juvenile patients with Pompe disease: a three-year open-label study.

van Capelle CI, van der Beek NA, Hagemans ML, Arts WF, Hop WC, Lee P, Jaeken J, Frohn-Mulder IM, Merkus PJ, Corzo D, Puga AC, Reuser AJ, van der Ploeg AT. van Capelle CI, et al. Among authors: arts wf. Neuromuscul Disord. 2010 Dec;20(12):775-82. doi: 10.1016/j.nmd.2010.07.277. Neuromuscul Disord. 2010. PMID: 20817528 Clinical Trial.

8

Enzyme therapy for pompe disease with recombinant human alpha-glucosidase from rabbit milk.

Van den Hout JM, Reuser AJ, de Klerk JB, Arts WF, Smeitink JA, Van der Ploeg AT. Van den Hout JM, et al. Among authors: arts wf. J Inherit Metab Dis. 2001 Apr;24(2):266-74. doi: 10.1023/a:1010383421286. J Inherit Metab Dis. 2001. PMID: 11405345 Clinical Trial.

9

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

10

Novel mutations in lysosomal neuraminidase identify functional domains and determine clinical severity in sialidosis.

Bonten EJ, Arts WF, Beck M, Covanis A, Donati MA, Parini R, Zammarchi E, d'Azzo A. Bonten EJ, et al. Among authors: arts wf. Hum Mol Genet. 2000 Nov 1;9(18):2715-25. doi: 10.1093/hmg/9.18.2715. Hum Mol Genet. 2000. PMID: 11063730

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