Parkinsonism in spinocerebellar ataxia with axonal neuropathy caused by adult-onset COA7 variants: a case report
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource, 1 online resource.
- Sprache
-
Englisch
- Erschienen in
-
Parkinsonism in spinocerebellar ataxia with axonal neuropathy caused by adult-onset COA7 variants: a case report ; volume:23 ; number:1 ; day:1 ; month:6 ; year:2023 ; pages:1-6 ; date:12.2023
BMC neurology ; 23, Heft 1 (1.6.2023), 1-6, 12.2023
- Urheber
-
Ouchi, Shogo
Ishii, Kazuhiro
Kosaki, Kenjiro
Suzuki, Hisato
Yamada, Mamiko
Takenouchi, Toshiki
Tamaoka, Akira
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s12883-023-03202-w
- URN
-
urn:nbn:de:101:1-2023091308130290431129
- Rechteinformation
-
Open Access; 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
- Ouchi, Shogo
- Ishii, Kazuhiro
- Kosaki, Kenjiro
- Suzuki, Hisato
- Yamada, Mamiko
- Takenouchi, Toshiki
- Tamaoka, Akira
- SpringerLink (Online service)
Ähnliche Objekte (12)
Mutations in MT-ATP6 are a frequent cause of adult-onset spinocerebellar ataxia
Spinocerebellar ataxia type 14 : refining clinicogenetic diagnosis in a rare adult-onset disorder
Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adult-onset disorder
Spinocerebellar ataxia: an update
Spinocerebellar Ataxia Type 2
Spinocerebellar ataxia type 31 (SCA31)
A Cysteinyl-tRNA Synthetase Mutation Causes Novel Autosomal-Dominant Inheritance of a Parkinsonism/Spinocerebellar-Ataxia Complex
Dysregulated pathways in spinocerebellar ataxia type 2 and ataxia telangectasia
Clinical analysis of adult-onset spinocerebellar ataxias in Thailand
Autonomic function testing in spinocerebellar ataxia type 2
Abnormal eye movements in spinocerebellar ataxia type 3
Spinocerebellar ataxia type 3 presenting simultaneously with motor neuron disease and cerebellar ataxia
Mutations in MT-ATP6 are a frequent cause of adult-onset spinocerebellar ataxia
Spinocerebellar ataxia type 14 : refining clinicogenetic diagnosis in a rare adult-onset disorder
Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adult-onset disorder
Spinocerebellar ataxia: an update
Spinocerebellar Ataxia Type 2
Spinocerebellar ataxia type 31 (SCA31)
A Cysteinyl-tRNA Synthetase Mutation Causes Novel Autosomal-Dominant Inheritance of a Parkinsonism/Spinocerebellar-Ataxia Complex
Dysregulated pathways in spinocerebellar ataxia type 2 and ataxia telangectasia
Clinical analysis of adult-onset spinocerebellar ataxias in Thailand
Autonomic function testing in spinocerebellar ataxia type 2
Abnormal eye movements in spinocerebellar ataxia type 3
Spinocerebellar ataxia type 3 presenting simultaneously with motor neuron disease and cerebellar ataxia
Mutations in MT-ATP6 are a frequent cause of adult-onset spinocerebellar ataxia
Spinocerebellar ataxia type 14 : refining clinicogenetic diagnosis in a rare adult-onset disorder
Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adult-onset disorder
Spinocerebellar ataxia: an update
Spinocerebellar Ataxia Type 2
Spinocerebellar ataxia type 31 (SCA31)
A Cysteinyl-tRNA Synthetase Mutation Causes Novel Autosomal-Dominant Inheritance of a Parkinsonism/Spinocerebellar-Ataxia Complex
Dysregulated pathways in spinocerebellar ataxia type 2 and ataxia telangectasia
Clinical analysis of adult-onset spinocerebellar ataxias in Thailand
Autonomic function testing in spinocerebellar ataxia type 2
Abnormal eye movements in spinocerebellar ataxia type 3