The difference in the diaphragmatic physiological measures between inspiratory and expiratory phases in ALS
Author:
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/s10072-022-06371-7.pdf
Reference36 articles.
1. Sarwal A, Walker FO, Cartwright MS (2013) Neuromuscular ultrasound for evaluation of the diaphragm. Muscle Nerve 47:319–329. https://doi.org/10.1002/mus.23671
2. Matsuda C, Shimizu T, Nakayama Y, Haraguchi M (2019) Cough peak flow decline rate predicts survival in patients with amyotrophic lateral sclerosis. Muscle Nerve 59:168–173. https://doi.org/10.1002/mus.26320
3. de Carvalho M, Swash M, Pinto S (2019) Diaphragmatic neurophysiology and Respiratory Markers in ALS. Front Neurol 10:143. https://doi.org/10.3389/fneur.2019.00143
4. Lechtzin N, Cudkowicz ME, de Carvalho M, Genge A, Hardiman O, Mitsumoto H, Mora JS et al (2018) Respiratory measures in amyotrophic lateral sclerosis. Amyotroph Lateral Scler Frontotemporal Degener 19:321–330. https://doi.org/10.1080/21678421.2018.1452945
5. Andersen PM, Borasio GD, Dengler R, Hardiman O, Kollewe K, Leigh PN, Pladat PF et al (2005) EFNS task force on management of amyotrophic lateral sclerosis: guidelines for diagnosing and clinical care of patients and relatives. Eur J Neurol 12:921–938. https://doi.org/10.1111/j.1468-1331.2011.03501.x
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