Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Acta Neuropsychiatrica|December 6, 2019
Intrinsic functional connectivity, CSF biomarker profiles and their relation to cognitive function in mild cognitive impairmentSilke Matura, Jan Köhler, Andreas Reif, et al.
Frontiers in Neurology|October 5, 2020
Comparing Programming Sessions of Vim-DBSSarah C Reitz, Sebastian Luger, Sriramya Lapa, et al.
Clinical Neurology and Neurosurgery|November 29, 2022
Necessity of MRI-compatible deep brain stimulation systems - Hits and hints for decision makingSarah Christina Reitz, Janina Lemmer-Etzrodt, Michael Eibach, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 12, 2020
High Glucosylceramides and Low Anandamide Contribute to Sensory Loss and Pain in Parkinson's DiseaseKatharina Klatt-Schreiner, Lucie Valek, Jun-Suk Kang, et al.
Neuroimage|July 28, 2009
Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6Jörg B Schulz, Johannes Borkert, Stefanie Wolf, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 2, 2006
Reliability and validity of the International Cooperative Ataxia Rating Scale: a study in 156 spinocerebellar ataxia patientsTanja Schmitz-Hübsch, Sophie Tezenas du Montcel, Laszlo Baliko, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 8, 2018
Postoperative rehabilitation after deep brain stimulation surgery for movement disordersNiels Allert, Binith Cheeran, Günther Deuschl, et al.
The Lancet. Neurology|May 28, 2013
Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline dataHeike Jacobi, Kathrin Reetz, Sophie Tezenas du Montcel, et al.
The Lancet. Neurology|August 22, 2020
Conversion of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 to manifest ataxia (RISCA): a longitudinal cohort studyHeike Jacobi, Sophie Tezenas du Montcel, Sandro Romanzetti, et al.
Neurology|August 11, 2017
Clinical and genetic characteristics of sporadic adult-onset degenerative ataxiaIlaria Giordano, Florian Harmuth, Heike Jacobi, et al.
Pageof 3