Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP)
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1750-1172
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP) ; volume:8 ; number:1 ; day:9 ; month:10 ; year:2013 ; pages:1-9 ; date:12.2013
Orphanet journal of rare diseases ; 8, Heft 1 (9.10.2013), 1-9, 12.2013
- Creator
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Karle, Kathrin N.
- Contributor
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Schüle-Freyer, Rebecca
Klebe, Stephan
Otto, Susanne
Frischholz, Christian
Liepelt-Scarfone, Inga
Schöls, Ludger
SpringerLink (Online service)
- DOI
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10.1186/1750-1172-8-158
- URN
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urn:nbn:de:1111-2016050122696
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:45 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Karle, Kathrin N.
- Schüle-Freyer, Rebecca
- Klebe, Stephan
- Otto, Susanne
- Frischholz, Christian
- Liepelt-Scarfone, Inga
- Schöls, Ludger
- SpringerLink (Online service)
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Hereditary spastic paraplegia from 1880 to 2017: an historical review
Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP)
Movement disorders in hereditary spastic paraplegia (HSP): a systematic review and individual participant data meta-analysis
Translational research approaches in hereditary spastic paraplegia
Early-onset hereditary spastic paraplegia: case report
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
Improving gait adaptability in patients with hereditary spastic paraplegia (Move-HSP): study protocol for a randomized controlled trial
New spastic paraplegia phenotype associated to mutation of NFU1
Understanding disease modulators of SPG11‐linked hereditary spastic paraplegia.
Gene identification in Hereditary Spastic Paraplegias and characterization of Spastic Paraplegia type 58 (SPG58)
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients
The role of inflammation in hereditary spastic paraplegia type 11
Hereditary spastic paraplegia from 1880 to 2017: an historical review
Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP)
Movement disorders in hereditary spastic paraplegia (HSP): a systematic review and individual participant data meta-analysis
Translational research approaches in hereditary spastic paraplegia
Early-onset hereditary spastic paraplegia: case report
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
Improving gait adaptability in patients with hereditary spastic paraplegia (Move-HSP): study protocol for a randomized controlled trial
New spastic paraplegia phenotype associated to mutation of NFU1
Understanding disease modulators of SPG11‐linked hereditary spastic paraplegia.
Gene identification in Hereditary Spastic Paraplegias and characterization of Spastic Paraplegia type 58 (SPG58)
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients
The role of inflammation in hereditary spastic paraplegia type 11