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Tatiana Svorenova

Showing results (1-10 of 6) with videos related to

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Parkinsonism & Related Disorders|July 22, 2025
Next move in movement disorders (NEMO): the best clinical tasks for the visibility of essential tremor, dystonia, cortical myoclonus and myoclonus-dystoniaGiorgia Sciacca, A M Madelein van der Stouwe, Liesanne M Centen, et al.
Computers in Biology and Medicine|May 9, 2025
Explainable machine learning for movement disorders - Classification of tremor and myoclonusElina L van den Brandhof, Inge Tuitert, A M Madelein van der Stouwe, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 24, 2023
Dystonia Linked to EIF4A2 Haploinsufficiency: A Disorder of Protein Translation DysfunctionPhilip Harrer, Matej Škorvánek, Volker Kittke, et al.
Research Square|June 10, 2024
p.L1795F LRRK2 variant is a common cause of Parkinson's disease in Central EuropeMiriam Ostrozovicova, Gertrud Tamas, Petr Dušek, et al.
Movement Disorders Clinical Practice|March 22, 2025
Prevalence and Clinical Characteristics of the LRRK2 p.L1795F Variant in Central Europeans with Early-Onset and Familial Parkinson's DiseaseMiriam Ostrozovicova, Gertrud Tamas, Agsha Atputhavadivel, et al.
Annals of Neurology|June 20, 2025
Deep Brain Stimulation for VPS16-Related Dystonia: A Multicenter StudyTatiana Svorenova, Luigi M Romito, Ahmet Kaymak, et al.
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Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Parkinsonism & Related Disorders|July 22, 2025
Next move in movement disorders (NEMO): the best clinical tasks for the visibility of essential tremor, dystonia, cortical myoclonus and myoclonus-dystoniaGiorgia Sciacca, A M Madelein van der Stouwe, Liesanne M Centen, et al.
Computers in Biology and Medicine|May 9, 2025
Explainable machine learning for movement disorders - Classification of tremor and myoclonusElina L van den Brandhof, Inge Tuitert, A M Madelein van der Stouwe, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 24, 2023
Dystonia Linked to EIF4A2 Haploinsufficiency: A Disorder of Protein Translation DysfunctionPhilip Harrer, Matej Škorvánek, Volker Kittke, et al.
Research Square|June 10, 2024
p.L1795F LRRK2 variant is a common cause of Parkinson's disease in Central EuropeMiriam Ostrozovicova, Gertrud Tamas, Petr Dušek, et al.
Movement Disorders Clinical Practice|March 22, 2025
Prevalence and Clinical Characteristics of the LRRK2 p.L1795F Variant in Central Europeans with Early-Onset and Familial Parkinson's DiseaseMiriam Ostrozovicova, Gertrud Tamas, Agsha Atputhavadivel, et al.
Annals of Neurology|June 20, 2025
Deep Brain Stimulation for VPS16-Related Dystonia: A Multicenter StudyTatiana Svorenova, Luigi M Romito, Ahmet Kaymak, et al.
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