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Michael Zech

Showing results (81-90 of 195) with videos related to

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Movement Disorders Clinical Practice|June 3, 2026
Atypical Atypical MECP2-Related Rett Syndrome Presenting with Movement Disorders- Predominating PhenotypeJán Necpál, Paula Stretavská, Elisabetta Indelicato, et al.
Parkinsonism & Related Disorders|July 13, 2020
Severe paroxysmal dyskinesias without epilepsy in a RHOBTB2 mutation carrierJán Necpál, Michael Zech, Alica Valachová, et al.
American Journal of Medical Genetics. Part A|June 16, 2025
The Attenuated Phenotype of CNTNAP1-Related Neuropathy Mimics Spastic-Dystonic Cerebral PalsyMagdalena Krygier, Michael Zech, Magdalena Chylińska, et al.
Neurogenetics|August 25, 2020
Familial writer's cramp: a clinical clue for inherited coenzyme Q<sub>10</sub> deficiencyMatthias Amprosi, Michael Zech, Ruth Steiger, et al.
The Science of the Total Environment|October 11, 2024
Using multi-proxy analysis to determine the long-term impacts of catchment dynamics on water reservoirs - A case from a tropical reservoir (Ruiru Basin Kenya)Esther Githumbi, Ann Kamamia, Lucas Kämpf, et al.
Scientific Reports|December 18, 2024
Late Glacial summer paleohydrology across Central EuropeMaximilian Prochnow, Johannes Hepp, Paul Strobel, et al.
Movement Disorders Clinical Practice|July 21, 2023
Challenges in Establishing the Diagnosis of <i>PRRT2</i>-Related Dystonia: Recurrent Pathogenic Variants in a Homopolymeric StretchIvana Dzinovic, Elisabeth Graf, Melanie Brugger, et al.
Clinical Parkinsonism & Related Disorders|September 3, 2024
Dystonia: A novel sign of the Smith-Magenis syndrome - A three-case reportLukáš Kunc, Petra Havránková, Matěj Škorvánek, et al.
Parkinsonism & Related Disorders|May 22, 2021
The rare and the common: An Austrian DRPLA family harboring the European haplotypeMatthias Amprosi, Michael Zech, Peter Lichtner, et al.
Movement Disorders Clinical Practice|April 2, 2026
Long-Term Benefit of GPi-DBS in Two Siblings with BCL11B-Related Dystonia: An Uncommon but Potentially Treatable ConditionVeronika Magocova, Tatiana Svorenova, Vladimir Han, et al.
Pageof 20

Showing results (81-90 of 195) with videos related to

Sort By:
Pageof 20
Movement Disorders Clinical Practice|June 3, 2026
Atypical Atypical MECP2-Related Rett Syndrome Presenting with Movement Disorders- Predominating PhenotypeJán Necpál, Paula Stretavská, Elisabetta Indelicato, et al.
Parkinsonism & Related Disorders|July 13, 2020
Severe paroxysmal dyskinesias without epilepsy in a RHOBTB2 mutation carrierJán Necpál, Michael Zech, Alica Valachová, et al.
American Journal of Medical Genetics. Part A|June 16, 2025
The Attenuated Phenotype of CNTNAP1-Related Neuropathy Mimics Spastic-Dystonic Cerebral PalsyMagdalena Krygier, Michael Zech, Magdalena Chylińska, et al.
Neurogenetics|August 25, 2020
Familial writer's cramp: a clinical clue for inherited coenzyme Q<sub>10</sub> deficiencyMatthias Amprosi, Michael Zech, Ruth Steiger, et al.
The Science of the Total Environment|October 11, 2024
Using multi-proxy analysis to determine the long-term impacts of catchment dynamics on water reservoirs - A case from a tropical reservoir (Ruiru Basin Kenya)Esther Githumbi, Ann Kamamia, Lucas Kämpf, et al.
Scientific Reports|December 18, 2024
Late Glacial summer paleohydrology across Central EuropeMaximilian Prochnow, Johannes Hepp, Paul Strobel, et al.
Movement Disorders Clinical Practice|July 21, 2023
Challenges in Establishing the Diagnosis of <i>PRRT2</i>-Related Dystonia: Recurrent Pathogenic Variants in a Homopolymeric StretchIvana Dzinovic, Elisabeth Graf, Melanie Brugger, et al.
Clinical Parkinsonism & Related Disorders|September 3, 2024
Dystonia: A novel sign of the Smith-Magenis syndrome - A three-case reportLukáš Kunc, Petra Havránková, Matěj Škorvánek, et al.
Parkinsonism & Related Disorders|May 22, 2021
The rare and the common: An Austrian DRPLA family harboring the European haplotypeMatthias Amprosi, Michael Zech, Peter Lichtner, et al.
Movement Disorders Clinical Practice|April 2, 2026
Long-Term Benefit of GPi-DBS in Two Siblings with BCL11B-Related Dystonia: An Uncommon but Potentially Treatable ConditionVeronika Magocova, Tatiana Svorenova, Vladimir Han, et al.
Pageof 20