Tijssen MA - Search Results

1

Association of BDNF Met66Met polymorphism with arm tremor in cervical dystonia.

Groen JL, Ritz K, Velseboer DC, Aramideh M, van Hilten JJ, Boon AJ, van de Warrenburg BP, Baas F, Tijssen MA. Groen JL, et al. Among authors: tijssen ma. Mov Disord. 2012 May;27(6):796-7. doi: 10.1002/mds.24922. Epub 2012 Jan 30. Mov Disord. 2012. PMID: 22290778 No abstract available.

2

Clinical and neurophysiological characterization of myoclonus in complex regional pain syndrome.

Munts AG, Van Rootselaar AF, Van Der Meer JN, Koelman JH, Van Hilten JJ, Tijssen MA. Munts AG, et al. Among authors: tijssen ma. Mov Disord. 2008 Mar 15;23(4):581-7. doi: 10.1002/mds.21910. Mov Disord. 2008. PMID: 18163455

3

Clinical and genetic characterization of a large Dutch family with primary focal dystonia.

Contarino MF, Berger-Plantinga E, Foncke EM, Ritz K, Mellema J, Baas F, Speelman JD, Tijssen MA. Contarino MF, et al. Among authors: tijssen ma. Mov Disord. 2008 Oct 30;23(14):1998-2003. doi: 10.1002/mds.22206. Mov Disord. 2008. PMID: 18823044

4

Myoclonus-dystonia: clinical and genetic evaluation of a large cohort.

Ritz K, Gerrits MC, Foncke EM, van Ruissen F, van der Linden C, Vergouwen MD, Bloem BR, Vandenberghe W, Crols R, Speelman JD, Baas F, Tijssen MA. Ritz K, et al. Among authors: tijssen ma. J Neurol Neurosurg Psychiatry. 2009 Jun;80(6):653-8. doi: 10.1136/jnnp.2008.162099. Epub 2008 Dec 9. J Neurol Neurosurg Psychiatry. 2009. PMID: 19066193

5

Screening for dystonia genes DYT1, 11 and 16 in patients with writer's cramp.

Ritz K, Groen JL, Kruisdijk JJ, Baas F, Koelman JH, Tijssen MA. Ritz K, et al. Among authors: tijssen ma. Mov Disord. 2009 Jul 15;24(9):1390-2. doi: 10.1002/mds.22632. Mov Disord. 2009. PMID: 19441135

6

Paramedical treatment in primary dystonia: a systematic review.

Delnooz CC, Horstink MW, Tijssen MA, van de Warrenburg BP. Delnooz CC, et al. Among authors: tijssen ma. Mov Disord. 2009 Nov 15;24(15):2187-98. doi: 10.1002/mds.22608. Mov Disord. 2009. PMID: 19839012 Review.

7

Late-onset Huntington disease with intermediate CAG repeats: true or false?

Groen JL, de Bie RM, Foncke EM, Roos RA, Leenders KL, Tijssen MA. Groen JL, et al. Among authors: tijssen ma. J Neurol Neurosurg Psychiatry. 2010 Feb;81(2):228-30. doi: 10.1136/jnnp.2008.170902. J Neurol Neurosurg Psychiatry. 2010. PMID: 20145031

8

DYT6 dystonia: mutation screening, phenotype, and response to deep brain stimulation.

Groen JL, Ritz K, Contarino MF, van de Warrenburg BP, Aramideh M, Foncke EM, van Hilten JJ, Schuurman PR, Speelman JD, Koelman JH, de Bie RM, Baas F, Tijssen MA. Groen JL, et al. Among authors: tijssen ma. Mov Disord. 2010 Oct 30;25(14):2420-7. doi: 10.1002/mds.23285. Mov Disord. 2010. PMID: 20687191

9

SGCE isoform characterization and expression in human brain: implications for myoclonus-dystonia pathogenesis?

Ritz K, van Schaik BD, Jakobs ME, van Kampen AH, Aronica E, Tijssen MA, Baas F. Ritz K, et al. Among authors: tijssen ma. Eur J Hum Genet. 2011 Apr;19(4):438-44. doi: 10.1038/ejhg.2010.206. Epub 2010 Dec 15. Eur J Hum Genet. 2011. PMID: 21157498 Free PMC article.

10

A new familial syndrome with dystonia and lower limb action myoclonus.

Groen J, van Rootselaar AF, van der Salm SM, Bloem BR, Tijssen M. Groen J, et al. Mov Disord. 2011 Apr;26(5):896-900. doi: 10.1002/mds.23557. Epub 2011 Mar 2. Mov Disord. 2011. PMID: 21370267

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