- Weitere Titel
-
Die Rolle von Entzündungsreaktionen bei hereditärer spastischer Paraplegie Typ 11
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
Würzburg, Universität Würzburg, Dissertation, 2023
- Schlagwort
-
Tiermodell
Maus
Entzündung
Immunmodulation
Nervendegeneration
- Ereignis
-
Veröffentlichung
- (wo)
-
Würzburg
- (wer)
-
Universität Würzburg
- (wann)
-
2024
- Urheber
- Beteiligte Personen und Organisationen
-
Martini, Rudolf
- DOI
-
10.25972/OPUS-30336
- URN
-
urn:nbn:de:bvb:20-opus-303368
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:54 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Hörner, Michaela
- Martini, Rudolf
- Universität Würzburg
Entstanden
- 2024
Ähnliche Objekte (12)
Translational research approaches in hereditary spastic paraplegia
Early-onset hereditary spastic paraplegia: case report
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
Gene identification in Hereditary Spastic Paraplegias and characterization of Spastic Paraplegia type 58 (SPG58)
Functional characterization of wild-type and N471D strumpellin in hereditary spastic paraplegia
Coexistence of Hereditary Spastic Paraplegia Type 4 and Narcolepsy: A Case Report
Potential markers for sample size estimations in hereditary spastic paraplegia type 5
Unravelling the mechanism of axonal degeneration in Hereditary Spastic Paraplegia type 7
Understanding disease modulators of SPG11‐linked hereditary spastic paraplegia.
Hereditary spastic paraplegia Type 4 (SPG4) : Disease pattern, disease progression and prognostic factors
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients
Hereditary spastic paraplegia from 1880 to 2017: an historical review
Translational research approaches in hereditary spastic paraplegia
Early-onset hereditary spastic paraplegia: case report
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
Gene identification in Hereditary Spastic Paraplegias and characterization of Spastic Paraplegia type 58 (SPG58)
Functional characterization of wild-type and N471D strumpellin in hereditary spastic paraplegia
Coexistence of Hereditary Spastic Paraplegia Type 4 and Narcolepsy: A Case Report
Potential markers for sample size estimations in hereditary spastic paraplegia type 5
Unravelling the mechanism of axonal degeneration in Hereditary Spastic Paraplegia type 7
Understanding disease modulators of SPG11‐linked hereditary spastic paraplegia.
Hereditary spastic paraplegia Type 4 (SPG4) : Disease pattern, disease progression and prognostic factors
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients
Hereditary spastic paraplegia from 1880 to 2017: an historical review
Translational research approaches in hereditary spastic paraplegia
Early-onset hereditary spastic paraplegia: case report
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
Gene identification in Hereditary Spastic Paraplegias and characterization of Spastic Paraplegia type 58 (SPG58)
Functional characterization of wild-type and N471D strumpellin in hereditary spastic paraplegia
Coexistence of Hereditary Spastic Paraplegia Type 4 and Narcolepsy: A Case Report
Potential markers for sample size estimations in hereditary spastic paraplegia type 5
Unravelling the mechanism of axonal degeneration in Hereditary Spastic Paraplegia type 7
Understanding disease modulators of SPG11‐linked hereditary spastic paraplegia.
Hereditary spastic paraplegia Type 4 (SPG4) : Disease pattern, disease progression and prognostic factors
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients