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Anne Weissbach

Showing results (61-70 of 72) with videos related to

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JAMA Neurology|December 4, 2018
Association of Pallidal Neurostimulation and Outcome Predictors With X-linked Dystonia ParkinsonismNorbert Brüggemann, Aloysius Domingo, Dirk Rasche, et al.
Parkinsonism & Related Disorders|October 28, 2022
Motor and psychiatric features in idiopathic blepharospasm: A data-driven cluster analysisGiovanni Defazio, Angelo F Gigante, Mark Hallett, et al.
Movement Disorders Clinical Practice|October 17, 2022
Measurement Properties of Clinical Scales Rating the Severity of Blepharospasm: A Multicenter Observational StudyGiovanni Defazio, Mark Hallett, Alfredo Berardelli, et al.
Parkinsonism & Related Disorders|December 28, 2024
Factor analysis and clustering of motor and psychiatric dimensions in idiopathic blepharospasmAngelo F Gigante, Mark Hallett, Hyder A Jinnah, et al.
Parkinsonism & Related Disorders|September 28, 2021
Diagnostic criteria for blepharospasm: A multicenter international studyGiovanni Defazio, Hyder A Jinnah, Alfredo Berardelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 16, 2021
Genotype-Phenotype Relations for the Atypical Parkinsonism Genes: MDSGene Systematic ReviewChristina Wittke, Sonja Petkovic, Valerija Dobricic, et al.
Neurology. Genetics|April 29, 2016
Clinical and genetic features of cervical dystonia in a large multicenter cohortMark S LeDoux, Satya R Vemula, Jianfeng Xiao, et al.
Genes|October 24, 2017
Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other DystoniasEva Hebert, Friederike Borngräber, Alexander Schmidt, et al.
International Journal of Molecular Sciences|May 14, 2025
Genotype-Phenotype Relations for the Dystonia-Parkinsonism Genes <i>GLB1</i>, <i>SLC6A3</i>, <i>SLC30A10</i>, <i>SLC39A14</i>, and <i>PLA2G6</i>: MDSGene Systematic ReviewJon Rodriguez-Antiguedad, Rajasumi Rajalingam, Clara Krüger, et al.
American Journal of Human Genetics|May 19, 2015
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaNiccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, et al.
Pageof 8

Showing results (61-70 of 72) with videos related to

Sort By:
Pageof 8
JAMA Neurology|December 4, 2018
Association of Pallidal Neurostimulation and Outcome Predictors With X-linked Dystonia ParkinsonismNorbert Brüggemann, Aloysius Domingo, Dirk Rasche, et al.
Parkinsonism & Related Disorders|October 28, 2022
Motor and psychiatric features in idiopathic blepharospasm: A data-driven cluster analysisGiovanni Defazio, Angelo F Gigante, Mark Hallett, et al.
Movement Disorders Clinical Practice|October 17, 2022
Measurement Properties of Clinical Scales Rating the Severity of Blepharospasm: A Multicenter Observational StudyGiovanni Defazio, Mark Hallett, Alfredo Berardelli, et al.
Parkinsonism & Related Disorders|December 28, 2024
Factor analysis and clustering of motor and psychiatric dimensions in idiopathic blepharospasmAngelo F Gigante, Mark Hallett, Hyder A Jinnah, et al.
Parkinsonism & Related Disorders|September 28, 2021
Diagnostic criteria for blepharospasm: A multicenter international studyGiovanni Defazio, Hyder A Jinnah, Alfredo Berardelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 16, 2021
Genotype-Phenotype Relations for the Atypical Parkinsonism Genes: MDSGene Systematic ReviewChristina Wittke, Sonja Petkovic, Valerija Dobricic, et al.
Neurology. Genetics|April 29, 2016
Clinical and genetic features of cervical dystonia in a large multicenter cohortMark S LeDoux, Satya R Vemula, Jianfeng Xiao, et al.
Genes|October 24, 2017
Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other DystoniasEva Hebert, Friederike Borngräber, Alexander Schmidt, et al.
International Journal of Molecular Sciences|May 14, 2025
Genotype-Phenotype Relations for the Dystonia-Parkinsonism Genes <i>GLB1</i>, <i>SLC6A3</i>, <i>SLC30A10</i>, <i>SLC39A14</i>, and <i>PLA2G6</i>: MDSGene Systematic ReviewJon Rodriguez-Antiguedad, Rajasumi Rajalingam, Clara Krüger, et al.
American Journal of Human Genetics|May 19, 2015
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaNiccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, et al.
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