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Katja Lohmann

Showing results (41-50 of 267) with videos related to

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Stem Cell Research|October 14, 2018
Generation and characterization of eight human-derived iPSC lines from affected and unaffected THAP1 mutation carriersHauke Baumann, Magdalena Jahn, Alexander Muenchau, et al.
Parkinsonism & Related Disorders|December 27, 2016
Evaluating the role of TMEM230 variants in Parkinson's diseaseHauke Baumann, Simone Wolff, Alexander Münchau, et al.
Brain and Behavior|May 3, 2022
Head impulse testing in bilateral vestibulopathy in patients with genetically defined CANVASMax Borsche, Vera Tadic, Inke R König, et al.
Journal of Neurogenetics|October 5, 2016
Dopamine DRD2 polymorphism (DRD2/ANNK1-Taq1A) is not a significant risk factor in writer's crampKirsten E Zeuner, Albert Acewicz, Arne Knutzen, et al.
Parkinsonism & Related Disorders|August 14, 2018
Field synopsis and systematic meta-analyses of genetic association studies in isolated dystoniaOlena Ohlei, Valerija Dobricic, Katja Lohmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 29, 2025
'What's in a Name?' Naming Genetically Determined Movement Disorders: Gap and ControversyConnie Marras, Alberto Albanese, Mark Hallett, et al.
Parkinson'S Disease|March 26, 2011
PINK1-Interacting Proteins: Proteomic Analysis of Overexpressed PINK1Aleksandar Rakovic, Anne Grünewald, Lisa Voges, et al.
European Journal of Human Genetics : EJHG|July 20, 2007
Role of ethnicity on the association of MAPT H1 haplotypes and subhaplotypes in Parkinson's diseaseSusan Winkler, Inke R König, Katja Lohmann-Hedrich, et al.
Journal of Parkinson'S Disease|May 2, 2022
Pronounced Orthostatic Hypotension in GBA-Related Parkinson's DiseaseTatiana Usnich, Henrike Hanssen, Katja Lohmann, et al.
Journal of Neurology|March 11, 2014
The recurrent mutation Arg258Gln in SYNJ1 (PARK20) is not a common cause of Parkinson's diseaseSusen Winkler, Eva-Juliane Vollstedt, Meike Kasten, et al.
Pageof 27

Showing results (41-50 of 267) with videos related to

Sort By:
Pageof 27
Stem Cell Research|October 14, 2018
Generation and characterization of eight human-derived iPSC lines from affected and unaffected THAP1 mutation carriersHauke Baumann, Magdalena Jahn, Alexander Muenchau, et al.
Parkinsonism & Related Disorders|December 27, 2016
Evaluating the role of TMEM230 variants in Parkinson's diseaseHauke Baumann, Simone Wolff, Alexander Münchau, et al.
Brain and Behavior|May 3, 2022
Head impulse testing in bilateral vestibulopathy in patients with genetically defined CANVASMax Borsche, Vera Tadic, Inke R König, et al.
Journal of Neurogenetics|October 5, 2016
Dopamine DRD2 polymorphism (DRD2/ANNK1-Taq1A) is not a significant risk factor in writer's crampKirsten E Zeuner, Albert Acewicz, Arne Knutzen, et al.
Parkinsonism & Related Disorders|August 14, 2018
Field synopsis and systematic meta-analyses of genetic association studies in isolated dystoniaOlena Ohlei, Valerija Dobricic, Katja Lohmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 29, 2025
'What's in a Name?' Naming Genetically Determined Movement Disorders: Gap and ControversyConnie Marras, Alberto Albanese, Mark Hallett, et al.
Parkinson'S Disease|March 26, 2011
PINK1-Interacting Proteins: Proteomic Analysis of Overexpressed PINK1Aleksandar Rakovic, Anne Grünewald, Lisa Voges, et al.
European Journal of Human Genetics : EJHG|July 20, 2007
Role of ethnicity on the association of MAPT H1 haplotypes and subhaplotypes in Parkinson's diseaseSusan Winkler, Inke R König, Katja Lohmann-Hedrich, et al.
Journal of Parkinson'S Disease|May 2, 2022
Pronounced Orthostatic Hypotension in GBA-Related Parkinson's DiseaseTatiana Usnich, Henrike Hanssen, Katja Lohmann, et al.
Journal of Neurology|March 11, 2014
The recurrent mutation Arg258Gln in SYNJ1 (PARK20) is not a common cause of Parkinson's diseaseSusen Winkler, Eva-Juliane Vollstedt, Meike Kasten, et al.
Pageof 27