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Katja Lohmann

Showing results (61-70 of 267) with videos related to

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Journal of Neurology|November 26, 2009
Rapid-onset dystonia-parkinsonism: case reportMarina Svetel, Laurie J Ozelius, Amber Buckley, et al.
Neurology. Genetics|September 27, 2016
Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disabilitySofia Steinrücke, Katja Lohmann, Aloysius Domingo, et al.
Journal of Neurology|November 1, 2014
Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females onlyRobert Wilcox, Ingrid Brænne, Norbert Brüggemann, et al.
Parkinsonism & Related Disorders|April 3, 2019
De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patientChristine Klein, Hauke Baumann, Luisa Olschewski, et al.
Human Molecular Genetics|May 29, 2010
Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patientsAleksandar Rakovic, Anne Grünewald, Philip Seibler, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 20, 2015
Mutations in TUBB4A and spastic paraplegiaKishore R Kumar, Franca Vulinovic, Katja Lohmann, et al.
Parkinsonism & Related Disorders|January 9, 2025
Insufficient effect of deep brain stimulation in a patient with KCNN2-associated myoclonus-dystoniaMartje G Pauly, Mirja Thomsen, Vera Tadic, et al.
Journal of Neurology|August 11, 2012
Genetic risk factors in Parkinson's disease: single gene effects and interactions of genotypesAnna Göbel, Eric A Macklin, Susen Winkler, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 30, 2023
In Vivo Investigation of Glucose Metabolism in Idiopathic and PRKN-Related Parkinson's DiseaseMax Borsche, Andre Märtens, Philipp Hörmann, et al.
Annals of Clinical and Translational Neurology|June 6, 2021
Zonisamide-responsive myoclonus in SEMA6B-associated progressive myoclonic epilepsyRebecca Herzog, Yorck Hellenbroich, Norbert Brüggemann, et al.
Pageof 27

Showing results (61-70 of 267) with videos related to

Sort By:
Pageof 27
Journal of Neurology|November 26, 2009
Rapid-onset dystonia-parkinsonism: case reportMarina Svetel, Laurie J Ozelius, Amber Buckley, et al.
Neurology. Genetics|September 27, 2016
Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disabilitySofia Steinrücke, Katja Lohmann, Aloysius Domingo, et al.
Journal of Neurology|November 1, 2014
Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females onlyRobert Wilcox, Ingrid Brænne, Norbert Brüggemann, et al.
Parkinsonism & Related Disorders|April 3, 2019
De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patientChristine Klein, Hauke Baumann, Luisa Olschewski, et al.
Human Molecular Genetics|May 29, 2010
Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patientsAleksandar Rakovic, Anne Grünewald, Philip Seibler, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 20, 2015
Mutations in TUBB4A and spastic paraplegiaKishore R Kumar, Franca Vulinovic, Katja Lohmann, et al.
Parkinsonism & Related Disorders|January 9, 2025
Insufficient effect of deep brain stimulation in a patient with KCNN2-associated myoclonus-dystoniaMartje G Pauly, Mirja Thomsen, Vera Tadic, et al.
Journal of Neurology|August 11, 2012
Genetic risk factors in Parkinson's disease: single gene effects and interactions of genotypesAnna Göbel, Eric A Macklin, Susen Winkler, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 30, 2023
In Vivo Investigation of Glucose Metabolism in Idiopathic and PRKN-Related Parkinson's DiseaseMax Borsche, Andre Märtens, Philipp Hörmann, et al.
Annals of Clinical and Translational Neurology|June 6, 2021
Zonisamide-responsive myoclonus in SEMA6B-associated progressive myoclonic epilepsyRebecca Herzog, Yorck Hellenbroich, Norbert Brüggemann, et al.
Pageof 27