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Vera Tadic

Showing results (1-10 of 43) with videos related to

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Movement Disorders Clinical Practice|March 15, 2019
How Do I Confirm that a New Mutation is Pathogenic?Joanne Trinh, Vera Tadic, Christine Klein
Neurology|January 17, 2018
Pearls & Oy-sters: Family history of Huntington disease disguised a case of dentatorubral-pallidoluysian atrophySinem Tunc, Vera Tadic, Christine Zühlke, et al.
Journal of Neurology|March 22, 2017
CAPN1 mutations are associated with a syndrome of combined spasticity and ataxiaVera Tadic, Christine Klein, Frauke Hinrichs, et al.
Antioxidants & Redox Signaling|November 21, 2013
Does uncoupling protein 2 expression qualify as marker of disease status in LRRK2-associated Parkinson's disease?Anne Grünewald, Björn Arns, Britta Meier, et al.
Archives of Neurology|September 19, 2012
Dopa-responsive dystonia revisited: diagnostic delay, residual signs, and nonmotor signsVera Tadic, Meike Kasten, Norbert Brüggemann, et al.
JAMA Neurology|February 17, 2015
Primary familial brain calcification with known gene mutations: a systematic review and challenges of phenotypic characterizationVera Tadic, Ana Westenberger, Aloysius Domingo, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|March 11, 2024
Impact of Physiotherapy in the Treatment of Pain in Cervical DystoniaClemens Jacksch, Sebastian Loens, Joerg Mueller, 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.
Parkinsonism & Related Disorders|January 22, 2014
Non-motor phenotype of dopa-responsive dystonia and quality of life assessmentNorbert Brüggemann, Sophie Stiller, Vera Tadic, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 16, 2016
Abnormal premotor-motor interaction in heterozygous Parkin- and Pink1 mutation carriersAnne Weissbach, Tobias Bäumer, Peter P Pramstaller, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
Movement Disorders Clinical Practice|March 15, 2019
How Do I Confirm that a New Mutation is Pathogenic?Joanne Trinh, Vera Tadic, Christine Klein
Neurology|January 17, 2018
Pearls & Oy-sters: Family history of Huntington disease disguised a case of dentatorubral-pallidoluysian atrophySinem Tunc, Vera Tadic, Christine Zühlke, et al.
Journal of Neurology|March 22, 2017
CAPN1 mutations are associated with a syndrome of combined spasticity and ataxiaVera Tadic, Christine Klein, Frauke Hinrichs, et al.
Antioxidants & Redox Signaling|November 21, 2013
Does uncoupling protein 2 expression qualify as marker of disease status in LRRK2-associated Parkinson's disease?Anne Grünewald, Björn Arns, Britta Meier, et al.
Archives of Neurology|September 19, 2012
Dopa-responsive dystonia revisited: diagnostic delay, residual signs, and nonmotor signsVera Tadic, Meike Kasten, Norbert Brüggemann, et al.
JAMA Neurology|February 17, 2015
Primary familial brain calcification with known gene mutations: a systematic review and challenges of phenotypic characterizationVera Tadic, Ana Westenberger, Aloysius Domingo, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|March 11, 2024
Impact of Physiotherapy in the Treatment of Pain in Cervical DystoniaClemens Jacksch, Sebastian Loens, Joerg Mueller, 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.
Parkinsonism & Related Disorders|January 22, 2014
Non-motor phenotype of dopa-responsive dystonia and quality of life assessmentNorbert Brüggemann, Sophie Stiller, Vera Tadic, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 16, 2016
Abnormal premotor-motor interaction in heterozygous Parkin- and Pink1 mutation carriersAnne Weissbach, Tobias Bäumer, Peter P Pramstaller, et al.
Pageof 5