Assessment of diaphragmatic function by ultrasonography in patients with systemic sclerosis and its relation to clinical parameters
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00508-023-02163-x.pdf
Reference35 articles.
1. Denton CP, Khanna D. Systemic sclerosis. Lancet. 2017;390:1685–99. https://doi.org/10.1016/S0140-6736(17)30933-9.
2. Ferri C, Valentini G, Cozzi F, Sebastiani M, Michelassi C, La Montagna G, et al. Systemic sclerosis: demographic, clinical, and serologic features and survival in 1,012 Italian patients. Medicine. 2002;81(2):139–53. https://doi.org/10.1097/00005792-200203000-00004.
3. Antoniou KM, Margaritopoulos GA, Goh NS, Karagiannis K, Desai SR, Nicholson AG, et al. Combined pulmonary fibrosis and emphysema in sclerodermarelated lung disease has a major confounding effect on lung physiology and screening for pulmonary hypertension. Arthritis Rheumatol. 2016;68(4):1004–12. https://doi.org/10.1002/art.39528.
4. Silva BRA, Rufino R, Costa CH, Vilela VS, Levy RA, Lopes AJ. Ventilation distribution and small airway function in patients with systemic sclerosis. Rev Port Pneumol. 2017;23(3):132–8. https://doi.org/10.1016/j.rppnen.2017.01.004.
5. Nawata T, Shirai Y, Suzuki M, Kuwana M. Chest wall muscle atrophy as a contributory factor for forced vital capacity decline in systemic sclerosis-associated interstitial lung disease. Baillieres Clin Rheumatol. 2021;60(1):250–5. https://doi.org/10.1093/rheumatology/keaa322.
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