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Katja Ritz

Showing results (1-10 of 17) with videos related to

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Parkinsonism & Related Disorders|April 29, 2014
DRD1 rare variants associated with tardive-like dystonia: a pilot pathway sequencing study in dystoniaJustus L Groen, Katja Ritz, Tom T Warner, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|August 22, 2013
Mouse models to study the effect of cardiovascular risk factors on brain structure and cognitionDiewertje I Bink, Katja Ritz, Eleonora Aronica, et al.
Circulation|October 15, 2014
Cause and mechanisms of intracranial atherosclerosisKatja Ritz, Nerissa P Denswil, Olga C G Stam, et al.
European Journal of Human Genetics : EJHG|December 16, 2010
SGCE isoform characterization and expression in human brain: implications for myoclonus-dystonia pathogenesis?Katja Ritz, Barbera Dc van Schaik, Marja E Jakobs, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 15, 2009
Screening for dystonia genes DYT1, 11 and 16 in patients with writer's crampKatja Ritz, Justus L Groen, Jose J M Kruisdijk, et al.
Genomics|June 1, 2011
Looking ultra deep: short identical sequences and transcriptional slippageKatja Ritz, Barbera D C van Schaik, Marja E Jakobs, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 1, 2008
Clinical and genetic characterization of a large Dutch family with primary focal dystoniaMaria Fiorella Contarino, Elles Berger-Plantinga, Elisabeth M J Foncke, et al.
Atherosclerosis|June 12, 2016
Atherosclerosis in the circle of Willis: Spatial differences in composition and in distribution of plaquesNerissa P Denswil, Allard C van der Wal, Katja Ritz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 6, 2013
Is TOR1A a risk factor in adult-onset primary torsion dystonia?Justus L Groen, Katja Ritz, Michael W Tanck, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 4, 2011
THAP1 mutations are infrequent in spasmodic dysphoniaJustus L Groen, Eren Yildirim, Katja Ritz, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Parkinsonism & Related Disorders|April 29, 2014
DRD1 rare variants associated with tardive-like dystonia: a pilot pathway sequencing study in dystoniaJustus L Groen, Katja Ritz, Tom T Warner, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|August 22, 2013
Mouse models to study the effect of cardiovascular risk factors on brain structure and cognitionDiewertje I Bink, Katja Ritz, Eleonora Aronica, et al.
Circulation|October 15, 2014
Cause and mechanisms of intracranial atherosclerosisKatja Ritz, Nerissa P Denswil, Olga C G Stam, et al.
European Journal of Human Genetics : EJHG|December 16, 2010
SGCE isoform characterization and expression in human brain: implications for myoclonus-dystonia pathogenesis?Katja Ritz, Barbera Dc van Schaik, Marja E Jakobs, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 15, 2009
Screening for dystonia genes DYT1, 11 and 16 in patients with writer's crampKatja Ritz, Justus L Groen, Jose J M Kruisdijk, et al.
Genomics|June 1, 2011
Looking ultra deep: short identical sequences and transcriptional slippageKatja Ritz, Barbera D C van Schaik, Marja E Jakobs, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 1, 2008
Clinical and genetic characterization of a large Dutch family with primary focal dystoniaMaria Fiorella Contarino, Elles Berger-Plantinga, Elisabeth M J Foncke, et al.
Atherosclerosis|June 12, 2016
Atherosclerosis in the circle of Willis: Spatial differences in composition and in distribution of plaquesNerissa P Denswil, Allard C van der Wal, Katja Ritz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 6, 2013
Is TOR1A a risk factor in adult-onset primary torsion dystonia?Justus L Groen, Katja Ritz, Michael W Tanck, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 4, 2011
THAP1 mutations are infrequent in spasmodic dysphoniaJustus L Groen, Eren Yildirim, Katja Ritz, et al.
Pageof 2