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Matthis Synofzik

Showing results (161-170 of 511) with videos related to

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Neurology|July 17, 2023
Frequency and Phenotype of <i>RFC1</i> Repeat Expansions in Bilateral VestibulopathyAndreas Traschütz, Felix Heindl, Muhammad Bilal, et al.
Cerebellum (London, England)|March 24, 2025
Smartphone Application for Spastic Ataxias Cross-Sectional Validation of a Newly Developed Smartphone App for Remote Monitoring in Spastic AtaxiasIlse H J Willemse, Sabato Mellone, Carlo Tacconi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2022
Specific Gait Changes in Prodromal Hereditary Spastic Paraplegia Type 4: preSPG4 StudyChristian Laßmann, Winfried Ilg, Marc Schneider, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 28, 2024
Digital Gait Measures Capture 1-Year Progression in Early-Stage Spinocerebellar Ataxia Type 2Jens Seemann, Lina Daghsen, Matthieu Cazier, et al.
Neurology and Therapy|January 13, 2025
Measurement Properties of the Friedreich Ataxia Rating Scale in Patients with Spinocerebellar AtaxiaMichele H Potashman, Evan Popoff, Lauren C Powell, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 7, 2016
Brain-computer interfacing in amyotrophic lateral sclerosis: Implications of a resting-state EEG analysisVinay Jayaram, Natalie Widmann, Christian Förster, et al.
Cerebellum (London, England)|August 24, 2019
Application of Quantitative Motor Assessments in Friedreich Ataxia and Evaluation of Their Relation to Clinical MeasuresChristian Hohenfeld, Imis Dogan, Robin Schubert, et al.
Cerebellum (London, England)|January 9, 2019
Fall Risk in Relation to Individual Physical Activity Exposure in Patients with Different Neurodegenerative Diseases: a Pilot StudyKarin Srulijes, Jochen Klenk, Michael Schwenk, et al.
Orphanet Journal of Rare Diseases|February 15, 2017
STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutationsStefanie Nicole Hayer, Tine Deconinck, Benjamin Bender, et al.
Orphanet Journal of Rare Diseases|November 5, 2018
Nerve ultrasound characterizes AMN polyneuropathy as inhomogeneous and focal hypertrophicTim W Rattay, Jennifer Just, Benjamin Röben, et al.
Pageof 52

Showing results (161-170 of 511) with videos related to

Sort By:
Pageof 52
Neurology|July 17, 2023
Frequency and Phenotype of <i>RFC1</i> Repeat Expansions in Bilateral VestibulopathyAndreas Traschütz, Felix Heindl, Muhammad Bilal, et al.
Cerebellum (London, England)|March 24, 2025
Smartphone Application for Spastic Ataxias Cross-Sectional Validation of a Newly Developed Smartphone App for Remote Monitoring in Spastic AtaxiasIlse H J Willemse, Sabato Mellone, Carlo Tacconi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2022
Specific Gait Changes in Prodromal Hereditary Spastic Paraplegia Type 4: preSPG4 StudyChristian Laßmann, Winfried Ilg, Marc Schneider, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 28, 2024
Digital Gait Measures Capture 1-Year Progression in Early-Stage Spinocerebellar Ataxia Type 2Jens Seemann, Lina Daghsen, Matthieu Cazier, et al.
Neurology and Therapy|January 13, 2025
Measurement Properties of the Friedreich Ataxia Rating Scale in Patients with Spinocerebellar AtaxiaMichele H Potashman, Evan Popoff, Lauren C Powell, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 7, 2016
Brain-computer interfacing in amyotrophic lateral sclerosis: Implications of a resting-state EEG analysisVinay Jayaram, Natalie Widmann, Christian Förster, et al.
Cerebellum (London, England)|August 24, 2019
Application of Quantitative Motor Assessments in Friedreich Ataxia and Evaluation of Their Relation to Clinical MeasuresChristian Hohenfeld, Imis Dogan, Robin Schubert, et al.
Cerebellum (London, England)|January 9, 2019
Fall Risk in Relation to Individual Physical Activity Exposure in Patients with Different Neurodegenerative Diseases: a Pilot StudyKarin Srulijes, Jochen Klenk, Michael Schwenk, et al.
Orphanet Journal of Rare Diseases|February 15, 2017
STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutationsStefanie Nicole Hayer, Tine Deconinck, Benjamin Bender, et al.
Orphanet Journal of Rare Diseases|November 5, 2018
Nerve ultrasound characterizes AMN polyneuropathy as inhomogeneous and focal hypertrophicTim W Rattay, Jennifer Just, Benjamin Röben, et al.
Pageof 52