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Mark S Ledoux

Showing results (81-90 of 125) with videos related to

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Brain Research. Molecular Brain Research|May 15, 2002
Molecular cloning and expression of rat torsinA in the normal and genetically dystonic (dt) ratPhilipp Ziefer, Joanne Leung, Tara Razzano, et al.
Parkinsonism & Related Disorders|March 2, 2012
Genotype-phenotype correlations in THAP1 dystonia: molecular foundations and description of new casesMark S LeDoux, Jianfeng Xiao, Monika Rudzińska, et al.
Neurobiology of Disease|November 29, 2016
Role of major and brain-specific Sgce isoforms in the pathogenesis of myoclonus-dystonia syndromeJianfeng Xiao, Satya R Vemula, Yi Xue, et al.
Plos Genetics|February 9, 2022
Ribosomal DNA promoter recognition is determined in vivo by cooperation between UBTF1 and SL1 and is compromised in the UBTF-E210K neuroregression syndromeMichel G Tremblay, Dany S Sibai, Melissa Valère, et al.
Annals of Neurology|March 27, 2012
Mutations in CIZ1 cause adult onset primary cervical dystoniaJianfeng Xiao, Ryan J Uitti, Yu Zhao, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 13, 2019
Long-term safety and efficacy of deutetrabenazine for the treatment of tardive dyskinesiaHubert H Fernandez, David Stamler, Mat D Davis, et al.
Neurology. Genetics|June 18, 2020
Genotyping single nucleotide polymorphisms for allele-selective therapy in Huntington diseaseDaniel O Claassen, Jody Corey-Bloom, E Ray Dorsey, et al.
Neurology|October 21, 2018
Predictors of alcohol responsiveness in dystoniaJohanna Junker, Valerie Brandt, Brian D Berman, et al.
Molecular Genetics & Genomic Medicine|May 18, 2018
Whole-exome sequencing for variant discovery in blepharospasmJun Tian, Satya R Vemula, Jianfeng Xiao, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 12, 2021
A Novel Variant of ATP5MC3 Associated with Both Dystonia and Spastic ParaplegiaDerek E Neilson, Michael Zech, Robert B Hufnagel, et al.
Pageof 13

Showing results (81-90 of 125) with videos related to

Sort By:
Pageof 13
Brain Research. Molecular Brain Research|May 15, 2002
Molecular cloning and expression of rat torsinA in the normal and genetically dystonic (dt) ratPhilipp Ziefer, Joanne Leung, Tara Razzano, et al.
Parkinsonism & Related Disorders|March 2, 2012
Genotype-phenotype correlations in THAP1 dystonia: molecular foundations and description of new casesMark S LeDoux, Jianfeng Xiao, Monika Rudzińska, et al.
Neurobiology of Disease|November 29, 2016
Role of major and brain-specific Sgce isoforms in the pathogenesis of myoclonus-dystonia syndromeJianfeng Xiao, Satya R Vemula, Yi Xue, et al.
Plos Genetics|February 9, 2022
Ribosomal DNA promoter recognition is determined in vivo by cooperation between UBTF1 and SL1 and is compromised in the UBTF-E210K neuroregression syndromeMichel G Tremblay, Dany S Sibai, Melissa Valère, et al.
Annals of Neurology|March 27, 2012
Mutations in CIZ1 cause adult onset primary cervical dystoniaJianfeng Xiao, Ryan J Uitti, Yu Zhao, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 13, 2019
Long-term safety and efficacy of deutetrabenazine for the treatment of tardive dyskinesiaHubert H Fernandez, David Stamler, Mat D Davis, et al.
Neurology. Genetics|June 18, 2020
Genotyping single nucleotide polymorphisms for allele-selective therapy in Huntington diseaseDaniel O Claassen, Jody Corey-Bloom, E Ray Dorsey, et al.
Neurology|October 21, 2018
Predictors of alcohol responsiveness in dystoniaJohanna Junker, Valerie Brandt, Brian D Berman, et al.
Molecular Genetics & Genomic Medicine|May 18, 2018
Whole-exome sequencing for variant discovery in blepharospasmJun Tian, Satya R Vemula, Jianfeng Xiao, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 12, 2021
A Novel Variant of ATP5MC3 Associated with Both Dystonia and Spastic ParaplegiaDerek E Neilson, Michael Zech, Robert B Hufnagel, et al.
Pageof 13