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Sensors (Basel, Switzerland)|June 19, 2024
Gait Variability as a Potential Motor Marker of Cerebellar Disease-Relationship between Variability of Stride, Arm Swing and Trunk Movements, and Walking SpeedDaniel Kroneberg, Astrid Nümann, Martina Minnerop, et al.Movement Disorders Clinical Practice|July 7, 2020
Functionally Relevant Maculopathy and Optic Atrophy in Spinocerebellar Ataxia Type 1Frederike Cosima Oertel, Oliver Zeitz, Maria Rönnefarth, et al.JMIR Human Factors|April 1, 2022
Proposal for Post Hoc Quality Control in Instrumented Motion Analysis Using Markerless Motion Capture: Development and Usability StudyHanna Marie Röhling, Patrik Althoff, Radina Arsenova, et al.Annals of Clinical and Translational Neurology|March 19, 2021
Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adult-onset disorderTanja Schmitz-Hübsch, Silke Lux, Peter Bauer, et al.Health and Quality of Life Outcomes|August 15, 2024
Converting PROMIS<sup>®</sup>-29 v2.0 profile data to SF-36 physical and mental component summary scores in patients with cardiovascular disordersGregor Liegl, Felix H Fischer, Carl N Martin, et al.Infection|July 11, 2023
Analysis of acute COVID-19 including chronic morbidity: protocol for the deep phenotyping National Pandemic Cohort Network in Germany (NAPKON-HAP)Fridolin Steinbeis, Charlotte Thibeault, Sarah Steinbrecher, et al.Nature Communications|February 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxiaBenita Menden, Rana D Incebacak Eltemur, German Demidov, et al.Pageof 2