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Beomseok Jeon

Showing results (191-200 of 199) with videos related to

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Journal of Neural Transmission (Vienna, Austria : 1996)|February 26, 2021
Consensus guidelines for botulinum toxin therapy: general algorithms and dosing tables for dystonia and spasticityDirk Dressler, Maria Concetta Altavista, Eckart Altenmueller, et al.
Movement Disorders Clinical Practice|April 10, 2024
Opicapone to Treat Early Wearing-off in Parkinson's Disease Patients: The Korean ADOPTION TrialJee-Young Lee, Hyeo-Il Ma, Joaquim J Ferreira, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 12, 2024
Large-Scale Screening: Phenotypic and Mutational Spectrum in Isolated and Combined Dystonia GenesMirja Thomsen, Katrin Marth, Sebastian Loens, et al.
Brain : a Journal of Neurology|November 3, 2020
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathyChin-Hsien Lin, Pei-I Tsai, Han-Yi Lin, et al.
Medrxiv : the Preprint Server for Health Sciences|July 17, 2025
Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's DiseaseLara M Lange, Zih-Hua Fang, Laurel Screven, et al.
Movement Disorders Clinical Practice|August 29, 2024
Exercise Habits in People with Parkinson's: A Multinational SurveyPriya Jagota, Phanupong Phutrakool, Nitish Kamble, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 11, 2025
Rare but Relevant? Assessing Variants in Dystonia-Linked Genes in Parkinson's DiseaseLara M Lange, Zih-Hua Fang, Laurel Screven, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
<i>GCH1</i> p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian PopulationsYi Wen Tay, Andrew Leslie Lee, Jie Ping Schee, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Genome-wide association study identifies a new susceptibility locus in <i>PLA2G4C</i> for Multiple System AtrophyYasuo Nakahara, Jun Mitsui, Hidetoshi Date, et al.
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Showing results (191-200 of 199) with videos related to

Sort By:
Pageof 20
You have reached the last page of results.This site can display upto 199 results.
Journal of Neural Transmission (Vienna, Austria : 1996)|February 26, 2021
Consensus guidelines for botulinum toxin therapy: general algorithms and dosing tables for dystonia and spasticityDirk Dressler, Maria Concetta Altavista, Eckart Altenmueller, et al.
Movement Disorders Clinical Practice|April 10, 2024
Opicapone to Treat Early Wearing-off in Parkinson's Disease Patients: The Korean ADOPTION TrialJee-Young Lee, Hyeo-Il Ma, Joaquim J Ferreira, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 12, 2024
Large-Scale Screening: Phenotypic and Mutational Spectrum in Isolated and Combined Dystonia GenesMirja Thomsen, Katrin Marth, Sebastian Loens, et al.
Brain : a Journal of Neurology|November 3, 2020
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathyChin-Hsien Lin, Pei-I Tsai, Han-Yi Lin, et al.
Medrxiv : the Preprint Server for Health Sciences|July 17, 2025
Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's DiseaseLara M Lange, Zih-Hua Fang, Laurel Screven, et al.
Movement Disorders Clinical Practice|August 29, 2024
Exercise Habits in People with Parkinson's: A Multinational SurveyPriya Jagota, Phanupong Phutrakool, Nitish Kamble, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 11, 2025
Rare but Relevant? Assessing Variants in Dystonia-Linked Genes in Parkinson's DiseaseLara M Lange, Zih-Hua Fang, Laurel Screven, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
<i>GCH1</i> p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian PopulationsYi Wen Tay, Andrew Leslie Lee, Jie Ping Schee, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Genome-wide association study identifies a new susceptibility locus in <i>PLA2G4C</i> for Multiple System AtrophyYasuo Nakahara, Jun Mitsui, Hidetoshi Date, et al.
Pageof 20