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Journal of Neurology
Published in: Journal of Neurology 1/2015

01-01-2015 | Letter to the Editors

Early and severe autonomic failure: broadening the clinical phenotype of type-2 spinocerebellar ataxia. A case report

Authors: R. Capozzo, G. Rizzo, M. De Mari, C. Tortorella, G. Logroscino

Published in: Journal of Neurology | Issue 1/2015

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Excerpt

Dear Sirs, …
Literature
1.
2.
De Joanna G, De Rosa A, Salvatore E et al (2008) Autonomic nervous system abnormalities in spinocerebellar ataxia type 2: a cardiovascular neurophysiologic study. J Neurol Sci 275:60–63CrossRefPubMed
3.
Filla A, De Michele G, Santoro L et al (1999) Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 families. J Neurol 246:467–471CrossRefPubMed
4.
Montes-Brown J, Machado A, Estévez M, Carricarte C, Velázquez-Pérez L (2012) Autonomic dysfunction in presymptomatic spinocerebellar ataxia type-2. Acta Neurol Scand 125:24–29CrossRefPubMed
5.
Sánchez-Cruz G, Velázquez-Pérez L, Gómez-Peña L, Martínez-Góngora E, Castellano-Sánchez G, Santos-Falcón N (2001) Dysautonomic features in patients with Cuban type 2 spinocerebellar ataxia. Rev Neurol 33:428–434PubMed
6.
Chen KH, Lin CH, Wu RM (2012) Psychotic-affective symptoms and multiple system atrophy expand phenotypes of spinocerebellar ataxia type 2. BMJ Case Rep. pii: bcr1020115061
7.
Nirenberg MJ, Libien J, Vonsattel JP, Fahn S (2007) Multiple system atrophy in a patient with the spinocerebellar ataxia 3 gene mutation. Mov Disord 22:251–254CrossRefPubMed
Metadata
Title
Early and severe autonomic failure: broadening the clinical phenotype of type-2 spinocerebellar ataxia. A case report
Authors
R. Capozzo
G. Rizzo
M. De Mari
C. Tortorella
G. Logroscino
Publication date
01-01-2015
Publisher
Springer Berlin Heidelberg
Published in
Journal of Neurology / Issue 1/2015
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-014-7577-3

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