Diagnosis and Treatment of Primary (Idiopathic) Dystonia

A. Albanese; F. Asmus; A. Berardelli; K. Bhatia; A. E. Elia; B. Elibol; G. Filippini; T. Gasser; J. K. Krauss; N. Nardocci; A. Newton; J. Valls-Solé; M. Vidailhet

doi:10.1002/9781444328394.ch12

Diagnosis and Treatment of Primary (Idiopathic) Dystonia

A. Albanese, F. Asmus, A. Berardelli, K. Bhatia, A. E. Elia, B. Elibol, G. Filippini, T. Gasser, J. K. Krauss, N. Nardocci, A. Newton, J. Valls-Solé, M. Vidailhet

Research output: Chapter in Book/Report/Conference proceeding › Chapter

Original language	English
Title of host publication	European Handbook of Neurological Management: Second Edition
Publisher	Wiley-Blackwell
Pages	191-206
Number of pages	16
Volume	1
ISBN (Print)	9781405185332
DOIs	https://doi.org/10.1002/9781444328394.ch12
Publication status	Published - Sep 6 2010

Keywords

Botulinum toxin treatment, continuing to be first choice treatment-for most types of focal dystonia
Brain imaging in diagnosis of dystonia
Classification of dystonia-based on three axes
Diagnosis and treatment of primary (idiopathic) dystonia
Dystonia, characterized by sustained muscle contractions-causing repetitive twisting movements or abnormal postures
DYT1 mutations, most important genetic cause-of early onset PPD worldwide
DYT12, rapid-onset dystonia-parkinsonism (RDP)-mutated gene, being ATP1A3
Long-term electrical stimulation of globus pallidus internus (GPi)-now established as an effective treatment for various types of dystonia
Most common form, DRD linked to GCH1 (GTPcyclohydrolase I) gene
Use of genetic test in diagnosis and counselling

ASJC Scopus subject areas

Neuroscience(all)

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10.1002/9781444328394.ch12

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Albanese, A., Asmus, F., Berardelli, A., Bhatia, K., Elia, A. E., Elibol, B., Filippini, G., Gasser, T., Krauss, J. K., Nardocci, N., Newton, A., Valls-Solé, J., & Vidailhet, M. (2010). Diagnosis and Treatment of Primary (Idiopathic) Dystonia. In European Handbook of Neurological Management: Second Edition (Vol. 1, pp. 191-206). Wiley-Blackwell. https://doi.org/10.1002/9781444328394.ch12

Albanese, A, Asmus, F, Berardelli, A, Bhatia, K, Elia, AE, Elibol, B, Filippini, G, Gasser, T, Krauss, JK, Nardocci, N, Newton, A, Valls-Solé, J & Vidailhet, M 2010, Diagnosis and Treatment of Primary (Idiopathic) Dystonia. in European Handbook of Neurological Management: Second Edition. vol. 1, Wiley-Blackwell, pp. 191-206. https://doi.org/10.1002/9781444328394.ch12

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AU - Albanese, A.

AU - Asmus, F.

AU - Berardelli, A.

AU - Bhatia, K.

AU - Elia, A. E.

AU - Elibol, B.

AU - Filippini, G.

AU - Gasser, T.

AU - Krauss, J. K.

AU - Nardocci, N.

AU - Newton, A.

AU - Valls-Solé, J.

AU - Vidailhet, M.

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KW - Classification of dystonia-based on three axes

KW - Diagnosis and treatment of primary (idiopathic) dystonia

KW - Dystonia, characterized by sustained muscle contractions-causing repetitive twisting movements or abnormal postures

KW - DYT1 mutations, most important genetic cause-of early onset PPD worldwide

KW - DYT12, rapid-onset dystonia-parkinsonism (RDP)-mutated gene, being ATP1A3

KW - Long-term electrical stimulation of globus pallidus internus (GPi)-now established as an effective treatment for various types of dystonia

KW - Most common form, DRD linked to GCH1 (GTPcyclohydrolase I) gene

KW - Use of genetic test in diagnosis and counselling

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Diagnosis and Treatment of Primary (Idiopathic) Dystonia

Keywords

ASJC Scopus subject areas

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