Zobrazeno 1 - 10
of 68
pro vyhledávání: '"restrictive ventilatory defect"'
Publikováno v:
Lung India, Vol 40, Iss 2, Pp 161-164 (2023)
Pulmonary alveolar microlithiasis (PAM) is a rare autosomal recessive disease characterised by the deposition of calcium phosphate microliths in the alveoli. PAM has been reported in all continents and there is often a familial history. There is clin
Externí odkaz:
https://doaj.org/article/6543320feecd4e45b84ffdc43e8b5a39
Autor:
Rucheng Chen, Jinna Zhang, Yaxian Pang, Qingping Liu, Jing Peng, Xiujuan Lin, Lingyong Cao, Weijia Gu, Lu Zhang, Ran Li, Qinghua Sun, Rong Zhang, Cuiqing Liu
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Fine particulate matter (PM2.5) is well known to impair lung function. Strategies protecting against PM2.5-exerted lung dysfunction have been less investigated. Qianjinweijing decoction (QJWJ), a decoction of a herbal medicine of natural origin, has
Externí odkaz:
https://doaj.org/article/3b7ff95d15184d53b1a4631bf0024721
Publikováno v:
Monaldi Archives for Chest Disease (2022)
The flow volume loop (FVL) is a graphic display of airflow against lung volumes at different levels obtained during the maximum inspiratory and expiratory maneuver. It is a simple and reproducible method of lung function assessment. A narrative revie
Externí odkaz:
https://doaj.org/article/a52acf3dbee04db9baabb45288312b02
Autor:
Nobutoshi Morimoto, Mizuki Morimoto, Yoshiaki Takahashi, Motonori Takamiya, Ichizo Nishino, Koji Abe
Publikováno v:
eNeurologicalSci, Vol 21, Iss , Pp 100284- (2020)
[Background] Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant muscle disease characterized by asymmetric involvement of muscles in the face, upper extremity, trunk, and lower extremity regions, with variable severity. It was rec
Externí odkaz:
https://doaj.org/article/793e918d96f0473696442477e11db7ae
Akademický článek
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Autor:
Sunil Chaudhry
Publikováno v:
Annals of Geriatric Education and Medical Sciences. 7:80-85
Idiopathic pulmonary fibrosis (IPF) is an interstitial lung disease characterised by chronic, progressive scarring of the lungs. It is a relatively rare disease, afflicting those 50–70 years of age, slightly more common among men than women, withou
Akademický článek
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Publikováno v:
IP Indian Journal of Clinical and Experimental Dermatology. 5:167-171
Introduction: Systemic Sclerosis (SSc) is a multi-system connective tissue disorder of unknown aetiology characterised by thickening and stiffening of skin. SSc is clinically classified as limited cutaneous systemic sclerosis (LCSSc) and diffuse cuta
Publikováno v:
B37. CASE REPORTS IN COUGH AND AIRWAYS DISEASE.
Autor:
Robert P. Baughman, Ogugua Ndili Obi
Publikováno v:
Chest. 158:1816-1817