Clinical characterization and natural history of ALS8/ <i>VAPB</i> p.Pro56Ser: upper motor neurone signs, survival, and functional milestones in 78 patients
- DOI
- 10.1080/21678421.2026.2674020
- Published
- 2026-05-21
- Container
- Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Publisher
- Informa UK Limited
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1080/21678421.2026.2674020,
title = {Clinical characterization and natural history of ALS8/
<i>VAPB</i>
p.Pro56Ser: upper motor neurone signs, survival, and functional milestones in 78 patients},
author = {Christian Marques Couto and Elisa De Melo Queiroz and Waneska Souza Lima and Savana Camilla De Lima Santos and Osvaldo José Moreira Nascimento},
year = {2026},
journal = {Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration},
doi = {10.1080/21678421.2026.2674020},
url = {https://doi.org/10.1080/21678421.2026.2674020}
}RIS
TY - JOUR
TI - Clinical characterization and natural history of ALS8/
<i>VAPB</i>
p.Pro56Ser: upper motor neurone signs, survival, and functional milestones in 78 patients
AU - Christian Marques Couto
AU - Elisa De Melo Queiroz
AU - Waneska Souza Lima
AU - Savana Camilla De Lima Santos
AU - Osvaldo José Moreira Nascimento
PY - 2026
JO - Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
DO - 10.1080/21678421.2026.2674020
UR - https://doi.org/10.1080/21678421.2026.2674020
ER - APA
Couto, C. M., Queiroz, E. D. M., Lima, W. S., Santos, S. C. D. L., & Nascimento, O. J. M. (2026). Clinical characterization and natural history of ALS8/ <i>VAPB</i> p.Pro56Ser: upper motor neurone signs, survival, and functional milestones in 78 patients. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. https://doi.org/10.1080/21678421.2026.2674020
Source records
- crossref · retrieved 2026-09-26T01:53:36.660Z