Hochschulschrift
Modelling SPG4-related hereditary spastic paraplegia using human induced pluripotent stem cells
- Alternative title
-
Die Etablierung eines Modells der SPG4 betreffenden Heriditären Spastischen Paraplegie basierend auf der Nutzung von humanen induzierten pluripotenten Stammzellen
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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In: Human Molecular Genetics
Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Diss., 2014
- Keyword
-
0
Hirnkrankheit
Neuropsychiatrie
Nervenkrankheit
- Event
-
Veröffentlichung
- (where)
-
Erlangen
- (who)
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Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
- (when)
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2014
- Creator
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Havlicek, Steven
- Contributor
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Winkler, Jürgen
Friedland, Kristina
Brandstätter, Johannes Helmut
- URN
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urn:nbn:de:bvb:29-opus4-49016
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 11:03 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.
Object type
- Hochschulschrift
Associated
- Havlicek, Steven
- Winkler, Jürgen
- Friedland, Kristina
- Brandstätter, Johannes Helmut
- Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
Time of origin
- 2014
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Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients
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Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
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Expression des CEA im ersten Trimenon der Schwangerschaft
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients
Automated assessment of foot elevation in adults with hereditary spastic paraplegia using inertial measurements and machine learning
Automated assessment of foot elevation in adults with hereditary spastic paraplegia using inertial measurements and machine learning
Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia
Translational research approaches in hereditary spastic paraplegia
Early-onset hereditary spastic paraplegia: case report
Understanding disease modulators of SPG11‐linked hereditary spastic paraplegia.
The role of inflammation in hereditary spastic paraplegia type 11
Modeling neurodevelopment and cortical dysfunction in SPG11-linked hereditary spastic paraplegia using human induced pluripotent stem cells
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
Neuropsychology and MRI correlates of neurodegeneration in SPG11 hereditary spastic paraplegia
Expression des CEA im ersten Trimenon der Schwangerschaft
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients
Automated assessment of foot elevation in adults with hereditary spastic paraplegia using inertial measurements and machine learning
Automated assessment of foot elevation in adults with hereditary spastic paraplegia using inertial measurements and machine learning
Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia
Translational research approaches in hereditary spastic paraplegia
Early-onset hereditary spastic paraplegia: case report
Understanding disease modulators of SPG11‐linked hereditary spastic paraplegia.