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Katja Lohmann

Showing results (131-140 of 267) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|May 3, 2012
Depression and quality of life in monogenic compared to idiopathic, early-onset Parkinson's diseaseMeike Kasten, Lena Kertelge, Vera Tadic, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 2010
Possible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15Anne Weissbach, Ana Djarmati, Christine Klein, et al.
Cerebellum (London, England)|March 24, 2026
Multi-Omics Characterization of a KIF1C Structural Variant in a Patient with a Complex Movement Disorder Partially Responsive to Deep Brain StimulationMirja Thomsen, Max Borsche, Vicente A Yépez, et al.
Journal of Neurology|November 21, 2019
Novel NAXE variants as a cause for neurometabolic disorder: implications for treatmentJoanne Trinh, Sophie Imhoff, Marija Dulovic-Mahlow, et al.
Human Mutation|June 17, 2014
Unraveling cellular phenotypes of novel TorsinA/TOR1A mutationsFranca Vulinovic, Katja Lohmann, Aleksandar Rakovic, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 28, 2016
Seemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxiaNataša Dragašević Mišković, Aloysius Domingo, Valerija Dobričić, et al.
Plos One|October 2, 2010
Mutant Parkin impairs mitochondrial function and morphology in human fibroblastsAnne Grünewald, Lisa Voges, Aleksandar Rakovic, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 26, 2026
Metabolic and Volumetric Alterations in the Basal Ganglia and the Cerebellum in Dopa-Responsive Dystonia in Symptomatic and Asymptomatic GCH1 Mutation CarriersJannik Prasuhn, Leon van Well, Marta M Pokotylo, et al.
Journal of Movement Disorders|December 20, 2022
A KMT2B Frameshift Variant Causing Focal Dystonia Restricted to the Oromandibular Region After Long-Term Follow-upAlfand Marl F. Dy Closas, Katja Lohmann, Ai Huey Tan, et al.
Human Mutation|November 24, 2019
Motor protein binding and mitochondrial transport are altered by pathogenic TUBB4A variantsFranca Vulinovic, Victor Krajka, Torben J Hausrat, et al.
Pageof 27

Showing results (131-140 of 267) with videos related to

Sort By:
Pageof 27
Movement Disorders : Official Journal of the Movement Disorder Society|May 3, 2012
Depression and quality of life in monogenic compared to idiopathic, early-onset Parkinson's diseaseMeike Kasten, Lena Kertelge, Vera Tadic, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 2010
Possible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15Anne Weissbach, Ana Djarmati, Christine Klein, et al.
Cerebellum (London, England)|March 24, 2026
Multi-Omics Characterization of a KIF1C Structural Variant in a Patient with a Complex Movement Disorder Partially Responsive to Deep Brain StimulationMirja Thomsen, Max Borsche, Vicente A Yépez, et al.
Journal of Neurology|November 21, 2019
Novel NAXE variants as a cause for neurometabolic disorder: implications for treatmentJoanne Trinh, Sophie Imhoff, Marija Dulovic-Mahlow, et al.
Human Mutation|June 17, 2014
Unraveling cellular phenotypes of novel TorsinA/TOR1A mutationsFranca Vulinovic, Katja Lohmann, Aleksandar Rakovic, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 28, 2016
Seemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxiaNataša Dragašević Mišković, Aloysius Domingo, Valerija Dobričić, et al.
Plos One|October 2, 2010
Mutant Parkin impairs mitochondrial function and morphology in human fibroblastsAnne Grünewald, Lisa Voges, Aleksandar Rakovic, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 26, 2026
Metabolic and Volumetric Alterations in the Basal Ganglia and the Cerebellum in Dopa-Responsive Dystonia in Symptomatic and Asymptomatic GCH1 Mutation CarriersJannik Prasuhn, Leon van Well, Marta M Pokotylo, et al.
Journal of Movement Disorders|December 20, 2022
A KMT2B Frameshift Variant Causing Focal Dystonia Restricted to the Oromandibular Region After Long-Term Follow-upAlfand Marl F. Dy Closas, Katja Lohmann, Ai Huey Tan, et al.
Human Mutation|November 24, 2019
Motor protein binding and mitochondrial transport are altered by pathogenic TUBB4A variantsFranca Vulinovic, Victor Krajka, Torben J Hausrat, et al.
Pageof 27