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Katja Lohmann

Showing results (151-160 of 267) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|April 16, 2011
Truncating mutations in THAP1 define the nuclear localization signalAlma Osmanovic, Andreas Dendorfer, Alev Erogullari, et al.
European Journal of Neurology|July 9, 2023
Genotype-phenotype relations for episodic ataxia genes: MDSGene systematic reviewDiana Angelika Olszewska, Aakash Shetty, Rajasumi Rajalingam, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 28, 2020
GBA Variants in Parkinson's Disease: Clinical, Metabolomic, and Multimodal Neuroimaging PhenotypesAndrea Greuel, Jean-Pierre Trezzi, Enrico Glaab, et al.
Annals of Neurology|February 22, 2026
Alternative Translation Initiation in PRKN Delays the Onset of Parkinson's Disease and Offers a Therapeutic TargetArian Hach, Katja Lohmann, Manabu Funayama, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 11, 2021
Multimodal Longitudinal Neurophysiological Investigations in Dopa-Responsive DystoniaAnne Weissbach, Annika Steinmeier, Martje G Pauly, et al.
Science Advances|May 14, 2025
The role of dopaminergic medication and specific pathway alterations in idiopathic and <i>PRKN/PINK1</i>-mediated Parkinson's diseaseAlexander Balck, Max Borsche, Philip Campbell, et al.
Neurology|September 3, 2013
Nonmotor and diagnostic findings in subjects with de novo Parkinson disease of the DeNoPa cohortBrit Mollenhauer, Ellen Trautmann, Friederike Sixel-Döring, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 25, 2021
Genotype-Phenotype Relations in Primary Familial Brain Calcification: Systematic MDSGene ReviewAlexander Balck, Susen Schaake, Neele Sophie Kuhnke, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 14, 2016
Reply letter to Jinnah "Locus pocus" and Albanese "Complex dystonia is not a category in the new 2013 consensus classification": Necessary evolution, no magic!Christine Klein, Anthony Lang, Bart P van de Warrenburg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 16, 2016
Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task forceConnie Marras, Anthony Lang, Bart P van de Warrenburg, et al.
Pageof 27

Showing results (151-160 of 267) with videos related to

Sort By:
Pageof 27
Movement Disorders : Official Journal of the Movement Disorder Society|April 16, 2011
Truncating mutations in THAP1 define the nuclear localization signalAlma Osmanovic, Andreas Dendorfer, Alev Erogullari, et al.
European Journal of Neurology|July 9, 2023
Genotype-phenotype relations for episodic ataxia genes: MDSGene systematic reviewDiana Angelika Olszewska, Aakash Shetty, Rajasumi Rajalingam, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 28, 2020
GBA Variants in Parkinson's Disease: Clinical, Metabolomic, and Multimodal Neuroimaging PhenotypesAndrea Greuel, Jean-Pierre Trezzi, Enrico Glaab, et al.
Annals of Neurology|February 22, 2026
Alternative Translation Initiation in PRKN Delays the Onset of Parkinson's Disease and Offers a Therapeutic TargetArian Hach, Katja Lohmann, Manabu Funayama, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 11, 2021
Multimodal Longitudinal Neurophysiological Investigations in Dopa-Responsive DystoniaAnne Weissbach, Annika Steinmeier, Martje G Pauly, et al.
Science Advances|May 14, 2025
The role of dopaminergic medication and specific pathway alterations in idiopathic and <i>PRKN/PINK1</i>-mediated Parkinson's diseaseAlexander Balck, Max Borsche, Philip Campbell, et al.
Neurology|September 3, 2013
Nonmotor and diagnostic findings in subjects with de novo Parkinson disease of the DeNoPa cohortBrit Mollenhauer, Ellen Trautmann, Friederike Sixel-Döring, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 25, 2021
Genotype-Phenotype Relations in Primary Familial Brain Calcification: Systematic MDSGene ReviewAlexander Balck, Susen Schaake, Neele Sophie Kuhnke, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 14, 2016
Reply letter to Jinnah "Locus pocus" and Albanese "Complex dystonia is not a category in the new 2013 consensus classification": Necessary evolution, no magic!Christine Klein, Anthony Lang, Bart P van de Warrenburg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 16, 2016
Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task forceConnie Marras, Anthony Lang, Bart P van de Warrenburg, et al.
Pageof 27