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Kathrin Hauser

Showing results (11-20 of 52) with videos related to

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Journal of Alzheimer'S Disease : JAD|September 23, 2010
Neprilysin activity in cerebrospinal fluid is associated with dementia and amyloid-β42 levels in Lewy body diseaseWalter Maetzler, Velichka Stoycheva, Benjamin Schmid, et al.
The European Journal of Neuroscience|March 8, 2012
Subthalamic nucleus stimulation restores the efferent cortical drive to muscle in parallel to functional motor improvementDaniel Weiss, Sorin Breit, Julia Hoppe, et al.
Journal of Alzheimer'S Disease : JAD|July 19, 2011
Serum and cerebrospinal fluid uric acid levels in lewy body disorders: associations with disease occurrence and amyloid-β pathwayWalter Maetzler, Anne Kathrin Stapf, Claudia Schulte, et al.
Journal of Medical Genetics|March 8, 2024
Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insightsBurcu Atasu, Javier Simón-Sánchez, Hasmet Hanagasi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 18, 2015
Mutations in CIZ1 are not a major cause for dystonia in GermanyClaudia Dufke, Ann-Kathrin Hauser, Marc Sturm, et al.
Frontiers in Microbiology|December 16, 2020
Fecal <i>Klebsiella pneumoniae</i> Carriage Is Intermittent and of High Clonal DiversitySarah Lepuschitz, Kathrin Hauser, Agnes Schriebl, et al.
Frontiers in Aging Neuroscience|September 21, 2018
Cholinergic Pathway SNPs and Postural Control in 477 Older AdultsCarina Arnold, Claudia Schulte, Mariana Moscovich, et al.
Parkinson'S Disease|August 19, 2017
Dual-Task Performance in GBA Parkinson's DiseaseKarin Srulijes, Kathrin Brockmann, Senait Ogbamicael, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|April 30, 2016
PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset ParkinsonismAnamika Giri, Gamze Guven, Hasmet Hanagasi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 27, 2018
HPCA confirmed as a genetic cause of DYT2-like dystonia phenotypeBurcu Atasu, Hasmet Hanagasi, Basar Bilgic, et al.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
Journal of Alzheimer'S Disease : JAD|September 23, 2010
Neprilysin activity in cerebrospinal fluid is associated with dementia and amyloid-β42 levels in Lewy body diseaseWalter Maetzler, Velichka Stoycheva, Benjamin Schmid, et al.
The European Journal of Neuroscience|March 8, 2012
Subthalamic nucleus stimulation restores the efferent cortical drive to muscle in parallel to functional motor improvementDaniel Weiss, Sorin Breit, Julia Hoppe, et al.
Journal of Alzheimer'S Disease : JAD|July 19, 2011
Serum and cerebrospinal fluid uric acid levels in lewy body disorders: associations with disease occurrence and amyloid-β pathwayWalter Maetzler, Anne Kathrin Stapf, Claudia Schulte, et al.
Journal of Medical Genetics|March 8, 2024
Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insightsBurcu Atasu, Javier Simón-Sánchez, Hasmet Hanagasi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 18, 2015
Mutations in CIZ1 are not a major cause for dystonia in GermanyClaudia Dufke, Ann-Kathrin Hauser, Marc Sturm, et al.
Frontiers in Microbiology|December 16, 2020
Fecal <i>Klebsiella pneumoniae</i> Carriage Is Intermittent and of High Clonal DiversitySarah Lepuschitz, Kathrin Hauser, Agnes Schriebl, et al.
Frontiers in Aging Neuroscience|September 21, 2018
Cholinergic Pathway SNPs and Postural Control in 477 Older AdultsCarina Arnold, Claudia Schulte, Mariana Moscovich, et al.
Parkinson'S Disease|August 19, 2017
Dual-Task Performance in GBA Parkinson's DiseaseKarin Srulijes, Kathrin Brockmann, Senait Ogbamicael, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|April 30, 2016
PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset ParkinsonismAnamika Giri, Gamze Guven, Hasmet Hanagasi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 27, 2018
HPCA confirmed as a genetic cause of DYT2-like dystonia phenotypeBurcu Atasu, Hasmet Hanagasi, Basar Bilgic, et al.
Pageof 6