Botulinum toxin treatment improves dysphagia in patients with oculopharyngeal muscular dystrophy and sporadic inclusion body myositis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
https://link.springer.com/content/pdf/10.1007/s00415-022-11028-8.pdf
Reference21 articles.
1. Schrey A, Airas L, Jokela M, Pulkkinen J (2017) Botulinum toxin alleviates dysphagia of patients with inclusion body myositis. J Neurol Sci 380:142–147
2. Oh TH, Brumfield KA, Hoskin TL, Stolp KA, Murray JA, Bassford JR (2007) Dysphagia in inflammatory myopathy: clinical characteristics, treatment strategies, and outcome in 62 patients. Mayo Clin Proc 82:441–447
3. Alonso-Jimenez A, Kroon R, Alejaldre-Monforte A et al (2019) Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy. J Neurol Neurosurg Psychiatry 90:576–585
4. Price MA, Barghout V, Benveniste O et al (2016) Mortality and causes of death in patients with sporadic inclusion body myositis: survey study based on the clinical experience of specialists in Australia, Europe and the USA. J Neuromuscul Dis 3:67–75
5. Taira K, Yamamoto T, Mori-Yoshimura M et al (2020) Obstruction-related dysphagia in inclusion body myositis: Cricopharyngeal bar on videofluoroscopy indicates risk of aspiration. J Neurol Sci 413:116764
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