Neurological management and outcome measures in Fabry disease: consensus statements from the Italian Fabry disease neurological working group
- DOI
- 10.1186/s13023-026-04361-y
- Published
- 2026-04-24
- Container
- Orphanet Journal of Rare Diseases
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1186/s13023-026-04361-y,
title = {Neurological management and outcome measures in Fabry disease: consensus statements from the Italian Fabry disease neurological working group},
author = {Michelangelo Mancuso and Alessandro Burlina and Leonardo Ulivi and Sirio Cocozza and Anna Bersano and Mirco Cosottini and Vincenzo Donadio and Antonello Giordano and Rocco Liguori and Renzo Manara and Anna Pichiecchio and Ilaria Romani and Antonio Siniscalchi and Maurizio Tenuta and Vittoria Cianci and Antonino Tuttolomondo},
year = {2026},
journal = {Orphanet Journal of Rare Diseases},
doi = {10.1186/s13023-026-04361-y},
url = {https://doi.org/10.1186/s13023-026-04361-y}
}RIS
TY - JOUR TI - Neurological management and outcome measures in Fabry disease: consensus statements from the Italian Fabry disease neurological working group AU - Michelangelo Mancuso AU - Alessandro Burlina AU - Leonardo Ulivi AU - Sirio Cocozza AU - Anna Bersano AU - Mirco Cosottini AU - Vincenzo Donadio AU - Antonello Giordano AU - Rocco Liguori AU - Renzo Manara AU - Anna Pichiecchio AU - Ilaria Romani AU - Antonio Siniscalchi AU - Maurizio Tenuta AU - Vittoria Cianci AU - Antonino Tuttolomondo PY - 2026 JO - Orphanet Journal of Rare Diseases DO - 10.1186/s13023-026-04361-y UR - https://doi.org/10.1186/s13023-026-04361-y ER -
APA
Mancuso, M., Burlina, A., Ulivi, L., Cocozza, S., Bersano, A., Cosottini, M., Donadio, V., Giordano, A., Liguori, R., Manara, R., Pichiecchio, A., Romani, I., Siniscalchi, A., Tenuta, M., Cianci, V., & Tuttolomondo, A. (2026). Neurological management and outcome measures in Fabry disease: consensus statements from the Italian Fabry disease neurological working group. Orphanet Journal of Rare Diseases. https://doi.org/10.1186/s13023-026-04361-y
Source records
- crossref · retrieved 2026-09-26T10:43:39.061Z