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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 paraplegia
Christian 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 Imaging
Christer 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 2
Natalie 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 polyneuropathy
Alexander 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 4
Christoph 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 paraplegias
Carlo 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 imaging
Tobias 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 ataxias
Dana M Bis, Rebecca Schüle, Jennifer Reichbauer, et al.
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of 5
Search research articles
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Showing results (11-20 of 47) with videos related to
Sort By:
Page
of 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 paraplegia
Christian 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 Imaging
Christer 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 2
Natalie 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 polyneuropathy
Alexander 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 4
Christoph 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 paraplegias
Carlo 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 imaging
Tobias 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 ataxias
Dana M Bis, Rebecca Schüle, Jennifer Reichbauer, et al.
Page
of 5