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Neuroimage. Clinical
|
October 29, 2015
Effects of rhythmic stimulus presentation on oscillatory brain activity: the physiology of cueing in Parkinson's disease
Erik S te Woerd, Robert Oostenveld, Bastiaan R Bloem, et al.
Annals of Clinical and Translational Neurology
|
July 30, 2020
The cerebral tremor circuit in a patient with Holmes tremor
Freek Nieuwhof, Rob M A de Bie, Peter Praamstra, et al.
Journal of Parkinson'S Disease
|
April 3, 2022
The Role of Microelectrode Recording and Stereotactic Computed Tomography in Verifying Lead Placement During Awake MRI-Guided Subthalamic Nucleus Deep Brain Stimulation for Parkinson's Disease
R Saman Vinke, Ashok K Selvaraj, Martin Geerlings, et al.
Parkinsonism & Related Disorders
|
September 26, 2020
A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene
Karlien Mul, Meyke I Schouten, Erica van der Looij, et al.
Journal of Medical Genetics
|
March 1, 2015
De novo gain-of-function and loss-of-function mutations of SCN8A in patients with intellectual disabilities and epilepsy
Maxime G Blanchard, Marjolein H Willemsen, Jaclyn B Walker, et al.
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of 5
Search research articles
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Showing results (41-50 of 45) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 45 results.
Neuroimage. Clinical
|
October 29, 2015
Effects of rhythmic stimulus presentation on oscillatory brain activity: the physiology of cueing in Parkinson's disease
Erik S te Woerd, Robert Oostenveld, Bastiaan R Bloem, et al.
Annals of Clinical and Translational Neurology
|
July 30, 2020
The cerebral tremor circuit in a patient with Holmes tremor
Freek Nieuwhof, Rob M A de Bie, Peter Praamstra, et al.
Journal of Parkinson'S Disease
|
April 3, 2022
The Role of Microelectrode Recording and Stereotactic Computed Tomography in Verifying Lead Placement During Awake MRI-Guided Subthalamic Nucleus Deep Brain Stimulation for Parkinson's Disease
R Saman Vinke, Ashok K Selvaraj, Martin Geerlings, et al.
Parkinsonism & Related Disorders
|
September 26, 2020
A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene
Karlien Mul, Meyke I Schouten, Erica van der Looij, et al.
Journal of Medical Genetics
|
March 1, 2015
De novo gain-of-function and loss-of-function mutations of SCN8A in patients with intellectual disabilities and epilepsy
Maxime G Blanchard, Marjolein H Willemsen, Jaclyn B Walker, et al.
Page
of 5