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Marina AJ Tijssen de Koning
Marina AJ Tijssen de Koning
Prof & Head of Movement Disorders, department of Neurology, University Medical Center Groningen
Verified email at umcg.nl - Homepage
Title
Cited by
Cited by
Year
Dopamine‐dependent changes in the functional connectivity between basal ganglia and cerebral cortex in humans
D Williams, M Tijssen, G Van Bruggen, A Bosch, A Insola, VD Lazzaro, ...
Brain 125 (7), 1558-1569, 2002
5872002
Mutations in the Na+/K+-ATPase α3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism
P de Carvalho Aguiar, KJ Sweadner, JT Penniston, J Zaremba, L Liu, ...
Neuron 43 (2), 169-175, 2004
5772004
Startle syndromes
MJ Bakker, JG Van Dijk, AMJM van den Maagdenberg, MAJ Tijssen
The Lancet Neurology 5 (6), 513-524, 2006
3072006
Double-blind clinical trial of thalamic stimulation in patients with Tourette syndrome
L Ackermans, A Duits, C van der Linden, M Tijssen, K Schruers, Y Temel, ...
Brain 134 (3), 832-844, 2011
2892011
The phenotypic spectrum of rapid-onset dystonia–parkinsonism (RDP) and mutations in the ATP1A3 gene
A Brashear, WB Dobyns, P de Carvalho Aguiar, M Borg, CJM Frijns, ...
Brain 130 (3), 828-835, 2007
2852007
Different functional loops between cerebral cortex and the subthalmic area in Parkinson's disease
N Fogelson, D Williams, M Tijssen, G van Bruggen, H Speelman, P Brown
Cerebral cortex 16 (1), 64-75, 2006
2642006
Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease
MI Rees, K Harvey, BR Pearce, SK Chung, IC Duguid, P Thomas, ...
Nature genetics 38 (7), 801-806, 2006
2352006
The anatomical basis of dystonia: current view using neuroimaging
S Lehéricy, MAJ Tijssen, M Vidailhet, R Kaji, S Meunier
Movement Disorders 28 (7), 944-957, 2013
2022013
Deep brain stimulation in Tourette's syndrome: two targets?
L Ackermans, Y Temel, D Cath, C van der Linden, R Bruggeman, ...
Movement disorders: official journal of the Movement Disorder Society 21 (5 …, 2006
1992006
Structural, functional and molecular imaging of the brain in primary focal dystonia—a review
E Zoons, J Booij, AJ Nederveen, JM Dijk, MAJ Tijssen
Neuroimage 56 (3), 1011-1020, 2011
1792011
Clinical spectrum of ataxia-telangiectasia in adulthood
MMM Verhagen, WF Abdo, M Willemsen, FBL Hogervorst, D Smeets, ...
Neurology 73 (6), 430-437, 2009
1782009
Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene
K Lohmann, RA Wilcox, S Winkler, A Ramirez, A Rakovic, JS Park, B Arns, ...
Annals of neurology 73 (4), 537-545, 2013
1752013
Presence of ATM protein and residual kinase activity correlates with the phenotype in ataxia‐telangiectasia: A genotype–phenotype study
MMM Verhagen, JI Last, FBL Hogervorst, DFCM Smeets, N Roeleveld, ...
Human mutation 33 (3), 561-571, 2012
1662012
The relationship between oscillatory activity and motor reaction time in the parkinsonian subthalamic nucleus
D Williams, A Kühn, A Kupsch, M Tijssen, G Van Bruggen, H Speelman, ...
European Journal of Neuroscience 21 (1), 249-258, 2005
1602005
Acute posthypoxic myoclonus after cardiopulmonary resuscitation
A Bouwes, D van Poppelen, JHTM Koelman, MA Kuiper, DF Zandstra, ...
BMC neurology 12, 1-6, 2012
1572012
Sepiapterin reductase deficiency: a treatable mimic of cerebral palsy
J Friedman, E Roze, JE Abdenur, R Chang, S Gasperini, V Saletti, ...
Annals of neurology 71 (4), 520-530, 2012
1572012
Behavioural cues are associated with modulations of synchronous oscillations in the human subthalamic nucleus
D Williams, A KuÈhn, A Kupsch, M Tijssen, G Van Bruggen, H Speelman, ...
Brain 126 (9), 1975-1985, 2003
1392003
Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3
RT Florian, F Kraft, E Leitão, S Kaya, S Klebe, E Magnin, ...
Nature communications 10 (1), 4919, 2019
1312019
DYT6 dystonia: mutation screening, phenotype, and response to deep brain stimulation
JL Groen, K Ritz, MF Contarino, BP van de Warrenburg, M Aramideh, ...
Movement disorders 25 (14), 2420-2427, 2010
1312010
Familial cortical myoclonic tremor with epilepsy: a single syndromic classification for a group of pedigrees bearing common features
AF Van Rootselaar, IN van Schaik, AMJM van den Maagdenberg, ...
Movement disorders: official journal of the Movement Disorder Society 20 (6 …, 2005
1242005
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