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Katja Lohmann

Showing results (21-30 of 267) with videos related to

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Parkinsonism & Related Disorders|February 19, 2017
A novel de-novo mutation in the ATP1A3 gene causing rapid-onset dystonia parkinsonismGregor R Wenzel, Katja Lohmann, Andrea A Kühn
Annual Review of Pathology|September 22, 2023
Genetics and Pathogenesis of DystoniaMirja Thomsen, Lara M Lange, Michael Zech, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|February 13, 2018
Novel SGCE mutation in a patient with myoclonus-dystonia syndrome - Diagnostic delay of more than 40 yearsDorothee Kübler, Friederike Borngräber, Katja Lohmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 20, 2023
MDSGene: Extending the List of Isolated Dystonia Genes by VPS16, EIF2AK2, and AOPEPMirja Thomsen, Lara M Lange, Christine Klein, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 30, 2011
Whispering dysphonia in an Australian family (DYT4): a clinical and genetic reappraisalRobert A Wilcox, Susen Winkler, Katja Lohmann, et al.
Neurology|February 5, 2017
Munchausen syndrome by genetics: Next-generation challenges for cliniciansSimone Zittel, Katja Lohmann, Peter Bauer, et al.
Neurobiology of Aging|January 15, 2014
Mutations in VPS26A are not a frequent cause of Parkinson's diseaseEva Koschmidder, Brit Mollenhauer, Meike Kasten, et al.
Journal of Neurology|April 30, 2017
Adult-onset ataxia or developmental disorder with seizures: two sides of missense changes in CACNA1AAlexander Balck, Henrike Hanssen, Yorck Hellenbroich, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 17, 2015
REM sleep-associated motor behaviors in Parkinson's disease patients with heterozygous Parkin mutationsFriederike Sixel-Döring, Katja Lohmann, Christine Klein, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 14, 2026
Reply to: "Revisiting Nomenclature in Movement Disorders: The Boundaries Between Pragmatism, Academicism, and Practical Applicability"Connie Marras, Alberto Albanese, Christine Klein, et al.
Pageof 27

Showing results (21-30 of 267) with videos related to

Sort By:
Pageof 27
Parkinsonism & Related Disorders|February 19, 2017
A novel de-novo mutation in the ATP1A3 gene causing rapid-onset dystonia parkinsonismGregor R Wenzel, Katja Lohmann, Andrea A Kühn
Annual Review of Pathology|September 22, 2023
Genetics and Pathogenesis of DystoniaMirja Thomsen, Lara M Lange, Michael Zech, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|February 13, 2018
Novel SGCE mutation in a patient with myoclonus-dystonia syndrome - Diagnostic delay of more than 40 yearsDorothee Kübler, Friederike Borngräber, Katja Lohmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 20, 2023
MDSGene: Extending the List of Isolated Dystonia Genes by VPS16, EIF2AK2, and AOPEPMirja Thomsen, Lara M Lange, Christine Klein, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 30, 2011
Whispering dysphonia in an Australian family (DYT4): a clinical and genetic reappraisalRobert A Wilcox, Susen Winkler, Katja Lohmann, et al.
Neurology|February 5, 2017
Munchausen syndrome by genetics: Next-generation challenges for cliniciansSimone Zittel, Katja Lohmann, Peter Bauer, et al.
Neurobiology of Aging|January 15, 2014
Mutations in VPS26A are not a frequent cause of Parkinson's diseaseEva Koschmidder, Brit Mollenhauer, Meike Kasten, et al.
Journal of Neurology|April 30, 2017
Adult-onset ataxia or developmental disorder with seizures: two sides of missense changes in CACNA1AAlexander Balck, Henrike Hanssen, Yorck Hellenbroich, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 17, 2015
REM sleep-associated motor behaviors in Parkinson's disease patients with heterozygous Parkin mutationsFriederike Sixel-Döring, Katja Lohmann, Christine Klein, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 14, 2026
Reply to: "Revisiting Nomenclature in Movement Disorders: The Boundaries Between Pragmatism, Academicism, and Practical Applicability"Connie Marras, Alberto Albanese, Christine Klein, et al.
Pageof 27