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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 disease
Walter 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 improvement
Daniel 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 pathway
Walter 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 insights
Burcu 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 Germany
Claudia 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 Diversity
Sarah Lepuschitz, Kathrin Hauser, Agnes Schriebl, et al.
Frontiers in Aging Neuroscience
|
September 21, 2018
Cholinergic Pathway SNPs and Postural Control in 477 Older Adults
Carina Arnold, Claudia Schulte, Mariana Moscovich, et al.
Parkinson'S Disease
|
August 19, 2017
Dual-Task Performance in GBA Parkinson's Disease
Karin 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 Parkinsonism
Anamika 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 phenotype
Burcu Atasu, Hasmet Hanagasi, Basar Bilgic, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 52) with videos related to
Sort By:
Page
of 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 disease
Walter 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 improvement
Daniel 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 pathway
Walter 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 insights
Burcu 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 Germany
Claudia 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 Diversity
Sarah Lepuschitz, Kathrin Hauser, Agnes Schriebl, et al.
Frontiers in Aging Neuroscience
|
September 21, 2018
Cholinergic Pathway SNPs and Postural Control in 477 Older Adults
Carina Arnold, Claudia Schulte, Mariana Moscovich, et al.
Parkinson'S Disease
|
August 19, 2017
Dual-Task Performance in GBA Parkinson's Disease
Karin 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 Parkinsonism
Anamika 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 phenotype
Burcu Atasu, Hasmet Hanagasi, Basar Bilgic, et al.
Page
of 6