Expanding SPG18 clinical spectrum: autosomal dominant mutation causes complicated hereditary spastic paraplegia in a large family
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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Expanding SPG18 clinical spectrum: autosomal dominant mutation causes complicated hereditary spastic paraplegia in a large family ; day:12 ; month:4 ; year:2024 ; pages:1-9
Neurological sciences ; (12.4.2024), 1-9
- Creator
-
Trinchillo, Assunta
Valente, Valeria
Esposito, Marcello
Migliaccio, Miriana
Iovino, Aniello
Picciocchi, Michele
Cuomo, Nunzia
Caccavale, Carmela
Nocerino, Cristofaro
Rosa, Laura De
Salvatore, Elena
Pierantoni, Giovanna Maria
Menchise, Valeria
Paladino, Simona
Criscuolo, Chiara
- Contributor
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SpringerLink (Online service)
- DOI
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10.1007/s10072-024-07500-0
- URN
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urn:nbn:de:101:1-2406252100131.203270016504
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 11:00 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
- Trinchillo, Assunta
- Valente, Valeria
- Esposito, Marcello
- Migliaccio, Miriana
- Iovino, Aniello
- Picciocchi, Michele
- Cuomo, Nunzia
- Caccavale, Carmela
- Nocerino, Cristofaro
- Rosa, Laura De
- Salvatore, Elena
- Pierantoni, Giovanna Maria
- Menchise, Valeria
- Paladino, Simona
- Criscuolo, Chiara
- SpringerLink (Online service)
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Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11
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Translational research approaches in hereditary spastic paraplegia
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Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia
Understanding disease modulators of SPG11‐linked hereditary spastic paraplegia.
Mania associated with complicated hereditary spastic paraparesis
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
Autosomal dominant hereditary spastic paraplegia: Novel mutations in the REEP1 gene (SPG31)
Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11
High frequency of SPG4 in Taiwanese families with autosomal dominant hereditary spastic paraplegia
Translational research approaches in hereditary spastic paraplegia
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Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia
Understanding disease modulators of SPG11‐linked hereditary spastic paraplegia.
Mania associated with complicated hereditary spastic paraparesis
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients
The role of inflammation in hereditary spastic paraplegia type 11