Diagnosis and pathogenesis of dystonia: clinical heterogeneity, shared mechanisms, and neurodevelopmental origins
- DOI
- 10.1016/s1474-4422(26)00098-0
- Published
- 2026-06
- Container
- The Lancet Neurology
- Publisher
- Elsevier BV
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/s1474-4422-26-00098-0,
title = {Diagnosis and pathogenesis of dystonia: clinical heterogeneity, shared mechanisms, and neurodevelopmental origins},
author = {Emmanuel Roze and Verity M McClelland and Lara M Lange and Hyder A Jinnah and Marie Vidailhet and Antonio Pisani},
year = {2026},
journal = {The Lancet Neurology},
doi = {10.1016/s1474-4422(26)00098-0},
url = {https://doi.org/10.1016/s1474-4422(26)00098-0}
}RIS
TY - JOUR TI - Diagnosis and pathogenesis of dystonia: clinical heterogeneity, shared mechanisms, and neurodevelopmental origins AU - Emmanuel Roze AU - Verity M McClelland AU - Lara M Lange AU - Hyder A Jinnah AU - Marie Vidailhet AU - Antonio Pisani PY - 2026 JO - The Lancet Neurology DO - 10.1016/s1474-4422(26)00098-0 UR - https://doi.org/10.1016/s1474-4422(26)00098-0 ER -
APA
Roze, E., McClelland, V. M., Lange, L. M., Jinnah, H. A., Vidailhet, M., & Pisani, A. (2026). Diagnosis and pathogenesis of dystonia: clinical heterogeneity, shared mechanisms, and neurodevelopmental origins. The Lancet Neurology. https://doi.org/10.1016/s1474-4422(26)00098-0
Source records
- crossref · retrieved 2026-09-26T06:12:07.796Z