Showing results (1-10 of 16) with videos related to
Sort By:
Pageof 2
Neurogenetics|April 3, 2012
Axonal transport deficit in a KIF5A( -/- ) mouse modelKathrin N Karle, Diana Möckel, Evan Reid, et al.Journal of Neurology|September 21, 2014
Imaging features in conventional MRI, spectroscopy and diffusion weighted images of hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS)Benjamin Bender, Uwe Klose, Tobias Lindig, et al.Orphanet Journal of Rare Diseases|October 11, 2013
Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP)Kathrin N Karle, Rebecca Schüle, Stephan Klebe, et al.European Journal of Clinical Pharmacology|October 18, 2014
Clozapine serum concentrations in dopamimetic psychosis in Parkinson's disease and related disordersUlrich C Lutz, Ahmad Sirfy, Gerlinde Wiatr, et al.Neurology|November 8, 2013
De novo mutations in hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS)Kathrin N Karle, Saskia Biskup, Rebecca Schüle, et al.Molecular Genetics & Genomic Medicine|October 22, 2014
AP5Z1/SPG48 frequency in autosomal recessive and sporadic spastic paraplegiaNina A Schlipf, Rebecca Schüle, Sven Klimpe, et al.Social Cognitive and Affective Neuroscience|January 25, 2018
Neurobiological correlates of emotional intelligence in voice and face perception networksKathrin N Karle, Thomas Ethofer, Heike Jacob, et al.Journal of Neurology|June 9, 2015
Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlationsTobias Lindig, Benjamin Bender, Till-Karsten Hauser, et al.Neurogenetics|October 16, 2008
Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegiaRebecca Schüle, Elisabeth Brandt, Kathrin N Karle, et al.Scientific Reports|July 28, 2017
DNA methylation signatures of chronic alcohol dependence in purified CD3+ T-cells of patients undergoing alcohol treatmentChristof Brückmann, Sumaiya A Islam, Julia L MacIsaac, et al.Pageof 2