The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Phenomenology and classification of dystonia: A consensus update
Open accessAbstract
This report describes the consensus outcome of an international panel consisting of investigators with years of experience in this field that reviewed the definition and classification of dystonia. Agreement was obtained based on a consensus development methodology during 3 in‐person meetings and manuscript review by mail. Dystonia is defined as a movement disorder characterized by sustained or intermittent muscle contractions causing abnormal, often repetitive, movements, postures, or both. Dystonic movements are typically patterned and twisting, and may be tremulous. Dystonia is often initiated or worsened by voluntary action and associated with overflow muscle activation. Dystonia is classified along 2 axes: clinical characteristics, including age at onset, body distribution, temporal pattern and associated features (additional movement disorders or neurological features); and etiology, which includes nervous system pathology and inheritance. The clinical characteristics fall into several specific dystonia syndromes that help to guide diagnosis and treatment. We provide here a new general definition of dystonia and propose a new classification. We encourage clinicians and researchers to use these innovative definition and classification and test them in the clinical setting on a variety of patients with dystonia. © 2013 Movement Disorder Society
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Citations
Cites
The non-motor syndrome of primary dystonia: clinical and pathophysiological implications
Stamelou, M., Edwards, M. J., Hallett, M., & Bhatia, K. P. (2012) · Brain · doi:10.1093/brain/awr224 · Cited by 299
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Cited by
Bhatia, K. P., Bain, P., Bajaj, N., Elble, R. J., Hallett, M., Louis, E. D., Raethjen, J., Stamelou, M., Testa, C. M., Deuschl, G., et al. (2018) · Movement Disorders · doi:10.1002/mds.27121 · Cited by 1,575
Self-citationDystonia as a network disorder: What is the role of the cerebellum?
Prudente, C. N., Hess, E. J., & Jinnah, H. A. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2013.11.062 · Cited by 262
Self-citationSex differences in movement disorders
Meoni, S., Macerollo, A., & Moro, E. (2020) · Nature Reviews Neurology · doi:10.1038/s41582-019-0294-x · Cited by 207
KCTD: A new gene family involved in neurodevelopmental and neuropsychiatric disorders
Teng, X., Aouacheria, A., Lionnard, L., Metz, K. A., Soane, L., Kamiya, A., & Hardwick, J. M. (2019) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13156 · Cited by 124
How to distinguish seizures from non-epileptic manifestations
Leibetseder, A., Eisermann, M., LaFrance, W. C., Nobili, L., & von Oertzen, T. J. (2020) · Epileptic Disorders · doi:10.1684/epd.2020.1234 · Cited by 93
Metadata
- Authors
- Albanese, A., Bhatia, K., Bressman, S. B., DeLong, M. R., Fahn, S., Fung, V. S. C., Hallett, M., Jankovic, J., Jinnah, H. A., Klein, C., Lang, A. E., Mink, J. W., & Teller, J. K.
- Venue
- Movement Disorders
- Publisher
- Wiley
- Published
- 2013-05-06
- Volume
- 28
- Issue
- 7
- Pages
- 863-873
- ISSN
- 0885-3185 (ISSN-L)
- 1531-8257
- OpenAlex
- W2131134103
- Cited by
- 2,265
- References
- 1
- FWCI
- 77.89
- Type
- journal article
- Language
- en
- Open access
- green
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- Albanese, A., Bhatia, K., Bressman, S. B., DeLong, M. R., Fahn, S., Fung, V. S. C., Hallett, M., Jankovic, J., Jinnah, H. A., Klein, C., Lang, A. E., Mink, J. W., & Teller, J. K. (2013). Phenomenology and classification of dystonia: A consensus update. Movement Disorders. https://doi.org/10.1002/mds.25475
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