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Mark S Ledoux

Showing results (71-80 of 125) with videos related to

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Neuroscience|September 6, 2020
Presynaptic PRRT2 Deficiency Causes Cerebellar Dysfunction and Paroxysmal Kinesigenic DyskinesiaDylan J Calame, Jianfeng Xiao, Mohammad Moshahid Khan, et al.
Experimental Neurology|April 30, 2019
Gnal haploinsufficiency causes genomic instability and increased sensitivity to haloperidolMohammad Moshahid Khan, Jianfeng Xiao, T J Hollingsworth, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|June 20, 2013
A randomized, double-blind study of repeated incobotulinumtoxinA (Xeomin(®)) in cervical dystoniaVirgilio Gerald H Evidente, Hubert H Fernandez, Mark S LeDoux, et al.
Genetics|August 25, 2005
Carbonic anhydrase-related protein VIII deficiency is associated with a distinctive lifelong gait disorder in waddles miceYan Jiao, Jian Yan, Yu Zhao, et al.
BMC Medical Genetics|July 16, 2013
Dystonia, facial dysmorphism, intellectual disability and breast cancer associated with a chromosome 13q34 duplication and overexpression of TFDP1: case reportMariana Moscovich, Mark S LeDoux, Jianfeng Xiao, et al.
Neuroimage. Clinical|June 11, 2020
Mapping typical and hypokinetic dysarthric speech production network using a connected speech paradigm in functional MRIShalini Narayana, Megan B Parsons, Wei Zhang, et al.
Frontiers in Neuroanatomy|June 18, 2015
The identification and neurochemical characterization of central neurons that target parasympathetic preganglionic neurons involved in the regulation of choroidal blood flow in the rat eye using pseudorabies virus, immunolabeling and conventional pathway tracing methodsChunyan Li, Malinda E C Fitzgerald, Nobel Del Mar, et al.
Experimental Neurology|May 11, 2016
Motor phenotypes and molecular networks associated with germline deficiency of Ciz1Jianfeng Xiao, Satya R Vemula, Yi Xue, et al.
Human Molecular Genetics|March 2, 2013
Role of Gα(olf) in familial and sporadic adult-onset primary dystoniaSatya R Vemula, Andreas Puschmann, Jianfeng Xiao, et al.
Neuroscience Letters|December 19, 2006
Effects of carbonic anhydrase VIII deficiency on cerebellar gene expression profiles in the wdl mouseJian Yan, Yan Jiao, Feng Jiao, et al.
Pageof 13

Showing results (71-80 of 125) with videos related to

Sort By:
Pageof 13
Neuroscience|September 6, 2020
Presynaptic PRRT2 Deficiency Causes Cerebellar Dysfunction and Paroxysmal Kinesigenic DyskinesiaDylan J Calame, Jianfeng Xiao, Mohammad Moshahid Khan, et al.
Experimental Neurology|April 30, 2019
Gnal haploinsufficiency causes genomic instability and increased sensitivity to haloperidolMohammad Moshahid Khan, Jianfeng Xiao, T J Hollingsworth, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|June 20, 2013
A randomized, double-blind study of repeated incobotulinumtoxinA (Xeomin(®)) in cervical dystoniaVirgilio Gerald H Evidente, Hubert H Fernandez, Mark S LeDoux, et al.
Genetics|August 25, 2005
Carbonic anhydrase-related protein VIII deficiency is associated with a distinctive lifelong gait disorder in waddles miceYan Jiao, Jian Yan, Yu Zhao, et al.
BMC Medical Genetics|July 16, 2013
Dystonia, facial dysmorphism, intellectual disability and breast cancer associated with a chromosome 13q34 duplication and overexpression of TFDP1: case reportMariana Moscovich, Mark S LeDoux, Jianfeng Xiao, et al.
Neuroimage. Clinical|June 11, 2020
Mapping typical and hypokinetic dysarthric speech production network using a connected speech paradigm in functional MRIShalini Narayana, Megan B Parsons, Wei Zhang, et al.
Frontiers in Neuroanatomy|June 18, 2015
The identification and neurochemical characterization of central neurons that target parasympathetic preganglionic neurons involved in the regulation of choroidal blood flow in the rat eye using pseudorabies virus, immunolabeling and conventional pathway tracing methodsChunyan Li, Malinda E C Fitzgerald, Nobel Del Mar, et al.
Experimental Neurology|May 11, 2016
Motor phenotypes and molecular networks associated with germline deficiency of Ciz1Jianfeng Xiao, Satya R Vemula, Yi Xue, et al.
Human Molecular Genetics|March 2, 2013
Role of Gα(olf) in familial and sporadic adult-onset primary dystoniaSatya R Vemula, Andreas Puschmann, Jianfeng Xiao, et al.
Neuroscience Letters|December 19, 2006
Effects of carbonic anhydrase VIII deficiency on cerebellar gene expression profiles in the wdl mouseJian Yan, Yan Jiao, Feng Jiao, et al.
Pageof 13