Predominant motor neuron involvement as a manifestation of pathogenic (full range) ATXN3 mutations
Author:
Funder
Gifts from the Donald G. and Jodi P. Heeringa Family.
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10072-022-06410-3.pdf
Reference5 articles.
1. Dong S, Zhu D, Yang W, Li J, Chen X (2022) Prominent lower motor neuron involvement in patients with intermediate-length CAG repeats in ATXN3 gene. Neurol Sci. https://doi.org/10.1007/s10072-022-06325-z
2. Rosini F, Pretegiani E, Battisti C, Dotti MT, Federico A, Rufa A (2020) Eye movement changes in autosomal dominant spinocerebellar ataxias. Neurol Sci 41(7):1719–1734. https://doi.org/10.1007/s10072-020-04318-4
3. Park JM, Kim SY, Park D, Park JS (2020) Effect of edaravone therapy in Korean amyotrophic lateral sclerosis (ALS) patients. Neurol Sci 41(1):119–123. https://doi.org/10.1007/s10072-019-04055-3
4. de Almeida FEO, do Carmo Santana AK, de Carvalho FO (2021) Multidisciplinary care in amyotrophic Lateral Sclerosis: a systematic review and meta-analysis. Neurol Sci 42(3):911–23. https://doi.org/10.1007/s10072-020-05011-2
5. Barć K, Kuźma-Kozakiewicz M (2020) Gastrostomy and mechanical ventilation in amyotrophic lateral sclerosis: how best to support the decision-making process? Neurol Neurochir Pol 54(5):366–377. https://doi.org/10.5603/PJNNS.a2020.0081
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