Marina A. J. Tijssen focuses on Neuroscience, Myoclonus, Dystonia, Genetics and Tics. Her work deals with themes such as Deep brain stimulation and Subthalamic nucleus, which intersect with Neuroscience. The study incorporates disciplines such as Somatosensory evoked potential, Neurology, Pediatrics, Neurological disorder and Epilepsy in addition to Myoclonus.
Her Dystonia study combines topics from a wide range of disciplines, such as Parkinsonism and Age of onset. Her study in the field of Mutation, Locus, Genetic linkage and Nonsense mutation is also linked to topics like Hyperekplexia. Her studies deal with areas such as Movement disorders, Tourette syndrome and Psychogenic disease as well as Tics.
The scientist’s investigation covers issues in Dystonia, Myoclonus, Movement disorders, Neuroscience and Physical medicine and rehabilitation. The Dystonia study combines topics in areas such as Physical therapy and Deep brain stimulation. The various areas that Marina A. J. Tijssen examines in her Myoclonus study include SGCE, Neurology, Pediatrics, Neurological disorder and Epilepsy.
Marina A. J. Tijssen works mostly in the field of Movement disorders, limiting it down to topics relating to Tics and, in certain cases, Tourette syndrome. Her work in the fields of Cerebellum, Basal ganglia, Local field potential and Electroencephalography overlaps with other areas such as Hyperekplexia. In her research on the topic of Cervical dystonia, Anesthesia is strongly related with Electromyography.
Marina A. J. Tijssen spends much of her time researching Dystonia, Movement disorders, Physical medicine and rehabilitation, Myoclonus and Neuroscience. Her Dystonia research is multidisciplinary, incorporating perspectives in Internal medicine, Tics, Deep brain stimulation and Anxiety. Her Movement disorders research integrates issues from Chorea, Pediatrics and Genetic testing.
Her work in the fields of Physical medicine and rehabilitation, such as Essential tremor, overlaps with other areas such as In patient. Her study in Myoclonus is interdisciplinary in nature, drawing from both SGCE, Back averaging, Parkinson's disease and Bioinformatics. Her work on Cortical myoclonus as part of her general Neuroscience study is frequently connected to Hyperekplexia, thereby bridging the divide between different branches of science.
Her primary areas of investigation include Dystonia, Quality of life, Movement disorders, Anxiety and Myoclonus. Her Dystonia study is associated with Neuroscience. Her Neuroscience study integrates concerns from other disciplines, such as Subthalamic nucleus and Medical genetics.
She combines subjects such as Functional movement and Randomized controlled trial with her study of Quality of life. Her biological study spans a wide range of topics, including Tics, Pediatrics and Reduced consciousness. Her work carried out in the field of Anxiety brings together such families of science as Cervical dystonia, Physical medicine and rehabilitation and Rating scale.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Dopamine-dependent changes in the functional connectivity between basal ganglia and cerebral cortex in humans
D Williams;M Tijssen;G van Bruggen;A Bosch.
Brain (2002)
Mutations in the Na+/K+-ATPase α3 Gene ATP1A3 Are Associated with Rapid-Onset Dystonia Parkinsonism
Patricia de Carvalho Aguiar;Patricia de Carvalho Aguiar;Kathleen J Sweadner;John T Penniston;Jacek Zaremba.
Neuron (2004)
The phenotypic spectrum of rapid-onset dystonia–parkinsonism (RDP) and mutations in the ATP1A3 gene
Allison Brashear;William B. Dobyns;Patricia de Carvalho Aguiar;Michel Borg.
Brain (2007)
Different Functional Loops between Cerebral Cortex and the Subthalmic Area in Parkinson's Disease
Noa Fogelson;David Williams;Marina Tijssen;Gerard van Bruggen.
Cerebral Cortex (2006)
Double-blind clinical trial of thalamic stimulation in patients with Tourette syndrome.
Linda Ackermans;Annelien Duits;Chris van der Linden;Marina A. Tijssen.
Brain (2011)
Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease.
Mark I. Rees;Mark I. Rees;Kirsten Harvey;Brian R. Pearce;Seo-Kyung Chung;Seo-Kyung Chung.
Nature Genetics (2006)
Deep brain stimulation in Tourette's syndrome: two targets?
Linda Ackermans;Yasin Temel;Danielle Cath;Chris van der Linden.
Movement Disorders (2006)
The anatomical basis of dystonia : current view using neuroimaging
Stéphane Lehéricy;Stéphane Lehéricy;Marina A.J. Tijssen;Marie Vidailhet;Ryuji Kaji.
Movement Disorders (2013)
Structural, functional and molecular imaging of the brain in primary focal dystonia-A review
Evelien Zoons;Jan Booij;Aart J. Nederveen;J. M. Dijk.
NeuroImage (2011)
Clinical spectrum of ataxia-telangiectasia in adulthood
M. M. M. Verhagen;W. F. Abdo;M. A. A. P. Willemsen;F. B. L. Hogervorst.
Neurology (2009)
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