Store-operated calcium entry is reduced in spastin-linked hereditary spastic paraplegia
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
In: 10.1093/brain/awac122
- Event
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Veröffentlichung
- (where)
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Aachen
- (who)
-
Universitätsbibliothek der RWTH Aachen
- (when)
-
2022
- Creator
-
Rizo, Tania
Gebhardt, Lisa
Riedlberger, Julia
Eberhardt, Esther
Fester, Lars
Alansary, Dalia
Winkler, Jurgen
Turan, Soeren
Arnold, Philipp
Niemeyer, Barbara A.
Fischer, Michael J. M.
Winner, Beate
- DOI
-
10.18154/RWTH-2022-08187
- URN
-
urn:nbn:de:101:1-2022112300372944449273
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:35 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
- Rizo, Tania
- Gebhardt, Lisa
- Riedlberger, Julia
- Eberhardt, Esther
- Fester, Lars
- Alansary, Dalia
- Winkler, Jurgen
- Turan, Soeren
- Arnold, Philipp
- Niemeyer, Barbara A.
- Fischer, Michael J. M.
- Winner, Beate
- Universitätsbibliothek der RWTH Aachen
Time of origin
- 2022
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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
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)
The role of the kinesin motor KIF1C in hereditary spastic paraplegia
Challenges and Controversies in the Genetic Diagnosis of Hereditary Spastic Paraplegia
Translational research approaches in hereditary spastic paraplegia
Early-onset hereditary spastic paraplegia: case report
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
Understanding disease modulators of SPG11‐linked hereditary spastic paraplegia.
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
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)
The role of the kinesin motor KIF1C in hereditary spastic paraplegia