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S Perlmutter

Showing results (541-550 of 570) with videos related to

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Movement Disorders Clinical Practice|February 11, 2022
Current Guidelines for Classifying and Diagnosing Cervical Dystonia: Empirical Evidence and RecommendationsGamze Kilic-Berkmen, Sarah Pirio Richardson, Joel S Perlmutter, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|August 15, 2016
HDQLIFE: development and assessment of health-related quality of life in Huntington disease (HD)N E Carlozzi, S G Schilling, J-S Lai, et al.
Dystonia (Lausanne, Switzerland)|November 8, 2024
Tremor in cervical dystoniaSinem Balta Beylergil, Krishna Nikhil Mukunda, Mohamed Elkasaby, et al.
Dystonia (Lausanne, Switzerland)|October 17, 2022
Clinical Features and Evolution of Blepharospasm: A Multicenter International Cohort and Systematic Literature ReviewLaura M Scorr, Hyun Joo Cho, Gamze Kilic-Berkmen, et al.
Neuron|March 31, 2026
Large-scale CSF and plasma proteomics reveal immune, synaptic, and extracellular matrix disruptions across neurodegenerative diseasesMuhammad Ali, Jigyasha Timsina, Ying Xu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 19, 2016
Clinical and demographic characteristics related to onset site and spread of cervical dystoniaScott A Norris, H A Jinnah, Alberto J Espay, et al.
European Journal of Neurology|July 23, 2021
Predictive modeling of spread in adult-onset isolated dystonia: Key properties and effect of tremor inclusionMeng Wang, Tolulope Sajobi, Francesca Morgante, et al.
Neurology|December 10, 2003
A haplotype at the PARK3 locus influences onset age for Parkinson's disease: the GenePD studyS Karamohamed, A L DeStefano, J B Wilk, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 21, 2005
Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD studySamer Karamohamed, L I Golbe, M H Mark, et al.
Brain : a Journal of Neurology|November 7, 2022
Mitochondrial haplogroups and cognitive progression in Parkinson's diseaseGanqiang Liu, Chunming Ni, Jiamin Zhan, et al.
Pageof 57

Showing results (541-550 of 570) with videos related to

Sort By:
Pageof 57
Movement Disorders Clinical Practice|February 11, 2022
Current Guidelines for Classifying and Diagnosing Cervical Dystonia: Empirical Evidence and RecommendationsGamze Kilic-Berkmen, Sarah Pirio Richardson, Joel S Perlmutter, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|August 15, 2016
HDQLIFE: development and assessment of health-related quality of life in Huntington disease (HD)N E Carlozzi, S G Schilling, J-S Lai, et al.
Dystonia (Lausanne, Switzerland)|November 8, 2024
Tremor in cervical dystoniaSinem Balta Beylergil, Krishna Nikhil Mukunda, Mohamed Elkasaby, et al.
Dystonia (Lausanne, Switzerland)|October 17, 2022
Clinical Features and Evolution of Blepharospasm: A Multicenter International Cohort and Systematic Literature ReviewLaura M Scorr, Hyun Joo Cho, Gamze Kilic-Berkmen, et al.
Neuron|March 31, 2026
Large-scale CSF and plasma proteomics reveal immune, synaptic, and extracellular matrix disruptions across neurodegenerative diseasesMuhammad Ali, Jigyasha Timsina, Ying Xu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 19, 2016
Clinical and demographic characteristics related to onset site and spread of cervical dystoniaScott A Norris, H A Jinnah, Alberto J Espay, et al.
European Journal of Neurology|July 23, 2021
Predictive modeling of spread in adult-onset isolated dystonia: Key properties and effect of tremor inclusionMeng Wang, Tolulope Sajobi, Francesca Morgante, et al.
Neurology|December 10, 2003
A haplotype at the PARK3 locus influences onset age for Parkinson's disease: the GenePD studyS Karamohamed, A L DeStefano, J B Wilk, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 21, 2005
Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD studySamer Karamohamed, L I Golbe, M H Mark, et al.
Brain : a Journal of Neurology|November 7, 2022
Mitochondrial haplogroups and cognitive progression in Parkinson's diseaseGanqiang Liu, Chunming Ni, Jiamin Zhan, et al.
Pageof 57