Verzijl H - Search Results

1

De novo mutations in PLXND1 and REV3L cause Möbius syndrome.

Tomas-Roca L, Tsaalbi-Shtylik A, Jansen JG, Singh MK, Epstein JA, Altunoglu U, Verzijl H, Soria L, van Beusekom E, Roscioli T, Iqbal Z, Gilissen C, Hoischen A, de Brouwer APM, Erasmus C, Schubert D, Brunner H, Pérez Aytés A, Marin F, Aroca P, Kayserili H, Carta A, de Wind N, Padberg GW, van Bokhoven H. Tomas-Roca L, et al. Among authors: verzijl h. Nat Commun. 2015 Jun 12;6:7199. doi: 10.1038/ncomms8199. Nat Commun. 2015. PMID: 26068067 Free PMC article.

2

Sequence analysis of the PLEXIN-D1 gene in Möbius syndrome patients.

van der Zwaag B, Verzijl HT, Wichers KH, Beltran-Valero de Bernabe D, Brunner HG, van Bokhoven H, Padberg GW. van der Zwaag B, et al. Among authors: verzijl ht. Pediatr Neurol. 2004 Aug;31(2):114-8. doi: 10.1016/j.pediatrneurol.2004.02.004. Pediatr Neurol. 2004. PMID: 15301830

3

Möbius syndrome redefined: a syndrome of rhombencephalic maldevelopment.

Verzijl HT, van der Zwaag B, Cruysberg JR, Padberg GW. Verzijl HT, et al. Neurology. 2003 Aug 12;61(3):327-33. doi: 10.1212/01.wnl.0000076484.91275.cd. Neurology. 2003. PMID: 12913192

4

Radiologic evidence for absence of the facial nerve in Möbius syndrome.

Verzijl HT, Valk J, de Vries R, Padberg GW. Verzijl HT, et al. Neurology. 2005 Mar 8;64(5):849-55. doi: 10.1212/01.WNL.0000152980.92436.D9. Neurology. 2005. PMID: 15753421

5

The spectrum of Mobius syndrome: an electrophysiological study.

Verzijl HT, Padberg GW, Zwarts MJ. Verzijl HT, et al. Brain. 2005 Jul;128(Pt 7):1728-36. doi: 10.1093/brain/awh502. Epub 2005 Apr 13. Brain. 2005. PMID: 15829555

6

Electrophysiological assessment in patients with Möbius syndrome and clumsiness.

Verzijl HT, Padberg GW, Zwarts MJ. Verzijl HT, et al. J Clin Neurophysiol. 2005 Dec;22(6):422-5. doi: 10.1097/01.WNP.0000179965.94248.B3. J Clin Neurophysiol. 2005. PMID: 16462200

7

Cognitive evaluation in adult patients with Möbius syndrome.

Verzijl HT, van Es N, Berger HJ, Padberg GW, van Spaendonck KP. Verzijl HT, et al. J Neurol. 2005 Feb;252(2):202-7. doi: 10.1007/s00415-005-0637-y. J Neurol. 2005. PMID: 15729527

8

The neuropathology of hereditary congenital facial palsy vs Möbius syndrome.

Verzijl HT, van der Zwaag B, Lammens M, ten Donkelaar HJ, Padberg GW. Verzijl HT, et al. Neurology. 2005 Feb 22;64(4):649-53. doi: 10.1212/01.WNL.0000151848.65094.55. Neurology. 2005. PMID: 15728286

9

A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch family.

Verzijl HT, van den Helm B, Veldman B, Hamel BC, Kuyt LP, Padberg GW, Kremer H. Verzijl HT, et al. Am J Hum Genet. 1999 Sep;65(3):752-6. doi: 10.1086/302539. Am J Hum Genet. 1999. PMID: 10441582 Free PMC article.

10

Mutation analysis in the candidate Möbius syndrome genes PGT and GATA2 on chromosome 3 and EGR2 on chromosome 10.

Van Der Zwaag B, Verzijl HT, Beltran-Valero De Bernabe D, Schuster VL, Van Bokhoven H, Kremer H, Van Reen M, Wichers GH, Brunner HG, Padberg GW. Van Der Zwaag B, et al. Among authors: verzijl ht. J Med Genet. 2002 Jun;39(6):E30. doi: 10.1136/jmg.39.6.e30. J Med Genet. 2002. PMID: 12070262 Free PMC article. No abstract available.

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