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Tim W Rattay

Showing results (11-20 of 47) with videos related to

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Journal of Neurology|October 25, 2019
Non-motor symptoms are relevant and possibly treatable in hereditary spastic paraplegia type 4 (SPG4)Tim W Rattay, Andreas Boldt, Maximilian Völker, et al.
Scientific Reports|December 21, 2022
Proof of principle for the clinical use of a CE-certified automatic imaging analysis tool in rare diseases studying hereditary spastic paraplegia type 4 (SPG4)Tobias Lindig, Benjamin Bender, Eva Bürkle, et al.
Journal of Neuroengineering and Rehabilitation|July 15, 2023
Dysfunctional neuro-muscular mechanisms explain gradual gait changes in prodromal spastic paraplegiaChristian Lassmann, Winfried Ilg, Tim W Rattay, et al.
Diagnostics (Basel, Switzerland)|August 28, 2025
Test-Retest Reliability and Inter-Scanner Reproducibility of Improved Spinal Diffusion Tensor ImagingChrister Ruff, Stephan König, Tim W Rattay, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 19, 2017
Ultrasound assessment of peripheral nerve pathology in neurofibromatosis type 1 and 2Natalie Winter, Tim W Rattay, Hubertus Axer, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|September 30, 2017
A look inside the nerve - Morphology of nerve fascicles in healthy controls and patients with polyneuropathyAlexander Grimm, Natalie Winter, Tim W Rattay, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|September 17, 2025
Serum NfL, but not GFAP, differentiates primary lateral sclerosis from adrenomyeloneuropathy and hereditary spastic paraplegia type 4Christoph Kessler, Carlo Wilke, Holger Hengel, et al.
Annals of Clinical and Translational Neurology|July 17, 2018
Serum neurofilament light chain is increased in hereditary spastic paraplegiasCarlo Wilke, Tim W Rattay, Holger Hengel, et al.
Neuroimage. Clinical|October 21, 2022
Detection of spinal long fiber tract degeneration in HSP: Improved diffusion tensor imagingTobias Lindig, Christer Ruff, Tim W Rattay, et al.
Molecular Genetics & Genomic Medicine|May 27, 2017
Uniparental disomy determined by whole-exome sequencing in a spectrum of rare motoneuron diseases and ataxiasDana M Bis, Rebecca Schüle, Jennifer Reichbauer, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
Journal of Neurology|October 25, 2019
Non-motor symptoms are relevant and possibly treatable in hereditary spastic paraplegia type 4 (SPG4)Tim W Rattay, Andreas Boldt, Maximilian Völker, et al.
Scientific Reports|December 21, 2022
Proof of principle for the clinical use of a CE-certified automatic imaging analysis tool in rare diseases studying hereditary spastic paraplegia type 4 (SPG4)Tobias Lindig, Benjamin Bender, Eva Bürkle, et al.
Journal of Neuroengineering and Rehabilitation|July 15, 2023
Dysfunctional neuro-muscular mechanisms explain gradual gait changes in prodromal spastic paraplegiaChristian Lassmann, Winfried Ilg, Tim W Rattay, et al.
Diagnostics (Basel, Switzerland)|August 28, 2025
Test-Retest Reliability and Inter-Scanner Reproducibility of Improved Spinal Diffusion Tensor ImagingChrister Ruff, Stephan König, Tim W Rattay, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 19, 2017
Ultrasound assessment of peripheral nerve pathology in neurofibromatosis type 1 and 2Natalie Winter, Tim W Rattay, Hubertus Axer, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|September 30, 2017
A look inside the nerve - Morphology of nerve fascicles in healthy controls and patients with polyneuropathyAlexander Grimm, Natalie Winter, Tim W Rattay, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|September 17, 2025
Serum NfL, but not GFAP, differentiates primary lateral sclerosis from adrenomyeloneuropathy and hereditary spastic paraplegia type 4Christoph Kessler, Carlo Wilke, Holger Hengel, et al.
Annals of Clinical and Translational Neurology|July 17, 2018
Serum neurofilament light chain is increased in hereditary spastic paraplegiasCarlo Wilke, Tim W Rattay, Holger Hengel, et al.
Neuroimage. Clinical|October 21, 2022
Detection of spinal long fiber tract degeneration in HSP: Improved diffusion tensor imagingTobias Lindig, Christer Ruff, Tim W Rattay, et al.
Molecular Genetics & Genomic Medicine|May 27, 2017
Uniparental disomy determined by whole-exome sequencing in a spectrum of rare motoneuron diseases and ataxiasDana M Bis, Rebecca Schüle, Jennifer Reichbauer, et al.
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