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Meike Kasten

Showing results (61-70 of 98) with videos related to

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Archives of Neurology|November 10, 2010
Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotypeNorbert Brüggemann, Johann Hagenah, Kathrin Reetz, et al.
Archives of Neurology|June 19, 2010
Nonmotor symptoms in genetic Parkinson diseaseMeike Kasten, Lena Kertelge, Norbert Brüggemann, 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|December 12, 2018
Utility and implications of exome sequencing in early-onset Parkinson's diseaseJoanne Trinh, Katja Lohmann, Hauke Baumann, et al.
Medrxiv : the Preprint Server for Health Sciences|January 2, 2026
How many do we miss? - Evaluation of age at onset and family history as selection criteria for genetic testing in Parkinson's diseaseAlexander Balck, Eva-Juliane Vollstedt, Ana Westenberger, et al.
Journal of Neurology|November 9, 2013
Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutationSarah Doss, Katja Lohmann, Philip Seibler, et al.
Archives of Neurology|July 18, 2012
Frequency of the D620N mutation in VPS35 in Parkinson diseaseKishore R Kumar, Anne Weissbach, Marcus Heldmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 27, 2021
Genotype-Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic ReviewLara M Lange, Johanna Junker, Sebastian Loens, et al.
Annals of Neurology|November 16, 2011
Solvent exposures and Parkinson disease risk in twinsSamuel M Goldman, Patricia J Quinlan, G Webster Ross, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 20, 2010
Impaired sense of smell and color discrimination in monogenic and idiopathic Parkinson's diseaseLena Kertelge, Norbert Brüggemann, Alexander Schmidt, et al.
Pageof 10

Showing results (61-70 of 98) with videos related to

Sort By:
Pageof 10
Archives of Neurology|November 10, 2010
Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotypeNorbert Brüggemann, Johann Hagenah, Kathrin Reetz, et al.
Archives of Neurology|June 19, 2010
Nonmotor symptoms in genetic Parkinson diseaseMeike Kasten, Lena Kertelge, Norbert Brüggemann, 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|December 12, 2018
Utility and implications of exome sequencing in early-onset Parkinson's diseaseJoanne Trinh, Katja Lohmann, Hauke Baumann, et al.
Medrxiv : the Preprint Server for Health Sciences|January 2, 2026
How many do we miss? - Evaluation of age at onset and family history as selection criteria for genetic testing in Parkinson's diseaseAlexander Balck, Eva-Juliane Vollstedt, Ana Westenberger, et al.
Journal of Neurology|November 9, 2013
Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutationSarah Doss, Katja Lohmann, Philip Seibler, et al.
Archives of Neurology|July 18, 2012
Frequency of the D620N mutation in VPS35 in Parkinson diseaseKishore R Kumar, Anne Weissbach, Marcus Heldmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 27, 2021
Genotype-Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic ReviewLara M Lange, Johanna Junker, Sebastian Loens, et al.
Annals of Neurology|November 16, 2011
Solvent exposures and Parkinson disease risk in twinsSamuel M Goldman, Patricia J Quinlan, G Webster Ross, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 20, 2010
Impaired sense of smell and color discrimination in monogenic and idiopathic Parkinson's diseaseLena Kertelge, Norbert Brüggemann, Alexander Schmidt, et al.
Pageof 10