Late-onset oro-facial dyskinesia in Spinocerebellar Ataxia type 2: a case report
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2377
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Late-onset oro-facial dyskinesia in Spinocerebellar Ataxia type 2: a case report ; volume:20 ; number:1 ; day:27 ; month:4 ; year:2020 ; pages:1-4 ; date:12.2020
BMC neurology ; 20, Heft 1 (27.4.2020), 1-4, 12.2020
- Urheber
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s12883-020-01739-8
- URN
-
urn:nbn:de:101:1-2020070521224057925607
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
- 14.08.2025, 10:44 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
- Giardina, Floriana
- Lanza, Giuseppe
- Calì, Francesco
- Ferri, Raffaele
- SpringerLink (Online service)
Ähnliche Objekte (12)
Spinocerebellar ataxia: an update
Spinocerebellar Ataxia Type 2
Spinocerebellar ataxia type 31 (SCA31)
Dysregulated pathways in spinocerebellar ataxia type 2 and ataxia telangectasia
Clinical and Biochemical Analysis of Glutamate-Cysteine Ligase Deficiency Presented with Late-Onset Spinocerebellar Ataxia and Hemolytic Anemia
Autonomic function testing in spinocerebellar ataxia type 2
Abnormal eye movements in spinocerebellar ataxia type 3
Neural correlates of ataxia severity in spinocerebellar ataxia type 3/Machado-Joseph disease
Spinocerebellar ataxia type 3 presenting simultaneously with motor neuron disease and cerebellar ataxia
Optimized testing strategy for the diagnosis of GAA-FGF14 ataxia/spinocerebellar ataxia 27B
Frequency of Spinocerebellar Ataxia type 1, 2, 3,6 and 7 and clinical profile of Spinocerebellar Ataxia type 3 in Malaysia
Epilepsy in spinocerebellar ataxia type 8: a case report
Spinocerebellar ataxia: an update
Spinocerebellar Ataxia Type 2
Spinocerebellar ataxia type 31 (SCA31)
Dysregulated pathways in spinocerebellar ataxia type 2 and ataxia telangectasia
Clinical and Biochemical Analysis of Glutamate-Cysteine Ligase Deficiency Presented with Late-Onset Spinocerebellar Ataxia and Hemolytic Anemia
Autonomic function testing in spinocerebellar ataxia type 2
Abnormal eye movements in spinocerebellar ataxia type 3
Neural correlates of ataxia severity in spinocerebellar ataxia type 3/Machado-Joseph disease
Spinocerebellar ataxia type 3 presenting simultaneously with motor neuron disease and cerebellar ataxia
Optimized testing strategy for the diagnosis of GAA-FGF14 ataxia/spinocerebellar ataxia 27B
Frequency of Spinocerebellar Ataxia type 1, 2, 3,6 and 7 and clinical profile of Spinocerebellar Ataxia type 3 in Malaysia
Epilepsy in spinocerebellar ataxia type 8: a case report
Spinocerebellar ataxia: an update
Spinocerebellar Ataxia Type 2
Spinocerebellar ataxia type 31 (SCA31)
Dysregulated pathways in spinocerebellar ataxia type 2 and ataxia telangectasia
Clinical and Biochemical Analysis of Glutamate-Cysteine Ligase Deficiency Presented with Late-Onset Spinocerebellar Ataxia and Hemolytic Anemia
Autonomic function testing in spinocerebellar ataxia type 2
Abnormal eye movements in spinocerebellar ataxia type 3
Neural correlates of ataxia severity in spinocerebellar ataxia type 3/Machado-Joseph disease
Spinocerebellar ataxia type 3 presenting simultaneously with motor neuron disease and cerebellar ataxia
Optimized testing strategy for the diagnosis of GAA-FGF14 ataxia/spinocerebellar ataxia 27B
Frequency of Spinocerebellar Ataxia type 1, 2, 3,6 and 7 and clinical profile of Spinocerebellar Ataxia type 3 in Malaysia