Corticospinal tract damage in HHH syndrome: a metabolic cause of hereditary spastic paraplegia
- 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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Corticospinal tract damage in HHH syndrome: a metabolic cause of hereditary spastic paraplegia ; volume:14 ; number:1 ; day:23 ; month:8 ; year:2019 ; pages:1-9 ; date:12.2019
Orphanet journal of rare diseases ; 14, Heft 1 (23.8.2019), 1-9, 12.2019
- Creator
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Olivieri, Giorgia
Pro, Stefano
Diodato, Daria
Di Capua, Matteo
Longo, Daniela
Martinelli, Diego
Bertini, Enrico
Dionisi-Vici, Carlo
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13023-019-1181-7
- URN
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urn:nbn:de:101:1-2020011900082189311867
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:56 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
- Olivieri, Giorgia
- Pro, Stefano
- Diodato, Daria
- Di Capua, Matteo
- Longo, Daniela
- Martinelli, Diego
- Bertini, Enrico
- Dionisi-Vici, Carlo
- SpringerLink (Online service)
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Gene identification in Hereditary Spastic Paraplegias and characterization of Spastic Paraplegia type 58 (SPG58)
The role of the kinesin motor KIF1C in hereditary spastic paraplegia
Ascending Axonal Degeneration of the Corticospinal Tract in Pure Hereditary Spastic Paraplegia: A Cross-Sectional DTI Study
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Understanding disease modulators of SPG11‐linked hereditary spastic paraplegia.
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients
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The role of inflammation in hereditary spastic paraplegia type 11
Non-pharmacological treatment of hereditary spastic paraplegia: a systematic review
Functional characterization of hereditary spastic paraplegia proteins spastin and ZFYVE27
Gene identification in Hereditary Spastic Paraplegias and characterization of Spastic Paraplegia type 58 (SPG58)