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Katja Ritz

Showing results (11-20 of 17) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|February 1, 2012
Association of BDNF Met66Met polymorphism with arm tremor in cervical dystoniaJustus L Groen, Katja Ritz, Daan C Velseboer, et al.
Journal of Cell Science|August 10, 2014
Actin-binding proteins differentially regulate endothelial cell stiffness, ICAM-1 function and neutrophil transmigrationAntje Schaefer, Joost Te Riet, Katja Ritz, et al.
Parkinsonism & Related Disorders|September 18, 2012
Cervical dystonia and genetic common variation in the dopamine pathwayJustus L Groen, Javier Simón-Sánchez, Katja Ritz, et al.
Human Molecular Genetics|October 10, 2014
CACNA1B mutation is linked to unique myoclonus-dystonia syndromeJustus L Groen, Arturo Andrade, Katja Ritz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 5, 2015
RELN rare variants in myoclonus-dystoniaJustus L Groen, Katja Ritz, Hamid Jalalzadeh, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 6, 2010
DYT6 dystonia: mutation screening, phenotype, and response to deep brain stimulationJustus L Groen, Katja Ritz, Maria Fiorella Contarino, et al.
Vascular Biology (Bristol, England)|January 15, 2025
Lack of intracranial atherosclerosis in various atherosclerotic mouse modelsDiewertje I Bink, Katja Ritz, Claire Mackaaij, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Movement Disorders : Official Journal of the Movement Disorder Society|February 1, 2012
Association of BDNF Met66Met polymorphism with arm tremor in cervical dystoniaJustus L Groen, Katja Ritz, Daan C Velseboer, et al.
Journal of Cell Science|August 10, 2014
Actin-binding proteins differentially regulate endothelial cell stiffness, ICAM-1 function and neutrophil transmigrationAntje Schaefer, Joost Te Riet, Katja Ritz, et al.
Parkinsonism & Related Disorders|September 18, 2012
Cervical dystonia and genetic common variation in the dopamine pathwayJustus L Groen, Javier Simón-Sánchez, Katja Ritz, et al.
Human Molecular Genetics|October 10, 2014
CACNA1B mutation is linked to unique myoclonus-dystonia syndromeJustus L Groen, Arturo Andrade, Katja Ritz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 5, 2015
RELN rare variants in myoclonus-dystoniaJustus L Groen, Katja Ritz, Hamid Jalalzadeh, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 6, 2010
DYT6 dystonia: mutation screening, phenotype, and response to deep brain stimulationJustus L Groen, Katja Ritz, Maria Fiorella Contarino, et al.
Vascular Biology (Bristol, England)|January 15, 2025
Lack of intracranial atherosclerosis in various atherosclerotic mouse modelsDiewertje I Bink, Katja Ritz, Claire Mackaaij, et al.
Pageof 2