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Page 1
Phenotypes and genetic architecture of focal primary torsion dystonia.
Groen JL, Kallen MC, van de Warrenburg BP, Speelman JD, van Hilten JJ, Aramideh M, Boon AJ, Klein C, Koelman JH, Langeveld TP, Baas F, Tijssen MA. Groen JL, et al. Among authors: baas f. J Neurol Neurosurg Psychiatry. 2012 Oct;83(10):1006-11. doi: 10.1136/jnnp-2012-302729. Epub 2012 Jul 8. J Neurol Neurosurg Psychiatry. 2012. PMID: 22773857
Cervical dystonia and genetic common variation in the dopamine pathway.
Groen JL, Simón-Sánchez J, Ritz K, Bochdanovits Z, Fang Y, van Hilten JJ, Aramideh M, van de Warrenburg BP, Boon AJ, Baas F, Heutink P, Tijssen MA. Groen JL, et al. Among authors: baas f. Parkinsonism Relat Disord. 2013 Mar;19(3):346-9. doi: 10.1016/j.parkreldis.2012.08.016. Epub 2012 Sep 14. Parkinsonism Relat Disord. 2013. PMID: 22981186
Is TOR1A a risk factor in adult-onset primary torsion dystonia?
Groen JL, Ritz K, Tanck MW, van de Warrenburg BP, van Hilten JJ, Aramideh M, Baas F, Tijssen MA. Groen JL, et al. Among authors: baas f. Mov Disord. 2013 Jun;28(6):827-31. doi: 10.1002/mds.25381. Epub 2013 Mar 4. Mov Disord. 2013. PMID: 23460578
RELN rare variants in myoclonus-dystonia.
Groen JL, Ritz K, Jalalzadeh H, van der Salm SM, Jongejan A, Mook OR, Haagmans MA, Zwinderman AH, Motazacker MM, Hennekam RC, Baas F, Tijssen MA. Groen JL, et al. Among authors: baas f. Mov Disord. 2015 Mar;30(3):415-9. doi: 10.1002/mds.26070. Epub 2015 Feb 4. Mov Disord. 2015. PMID: 25648840
Phenotype-genotype correlation in Dutch patients with myoclonus-dystonia.
Gerrits MC, Foncke EM, de Haan R, Hedrich K, van de Leemput YL, Baas F, Ozelius LJ, Speelman JD, Klein C, Tijssen MA. Gerrits MC, et al. Among authors: baas f. Neurology. 2006 Mar 14;66(5):759-61. doi: 10.1212/01.wnl.0000201192.66467.a3. Neurology. 2006. PMID: 16534121
417 results