Lower respiratory infection and inflammation in infants with newly diagnosed cystic fibrosis.
作者信息
Armstrong D S, Grimwood K, Carzino R, Carlin J B, Olinsky A, Phelan P D
机构信息
Department of Thoracic Medicine, Royal Children's Hospital, University of Melbourne, Parkville, Victoria, Australia.
出版信息
BMJ. 1995 Jun 17;310(6994):1571-2. doi: 10.1136/bmj.310.6994.1571.
Abstract
摘要
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本文引用的文献
1
Bronchoalveolar lavage findings in cystic fibrosis patients with stable, clinically mild lung disease suggest ongoing infection and inflammation.患有稳定的、临床症状较轻的肺部疾病的囊性纤维化患者的支气管肺泡灌洗结果提示存在持续感染和炎症。
Am J Respir Crit Care Med. 1994 Aug;150(2):448-54. doi: 10.1164/ajrccm.150.2.8049828.
2
Protease-antiprotease imbalance in the lungs of children with cystic fibrosis.囊性纤维化患儿肺部的蛋白酶-抗蛋白酶失衡
Am J Respir Crit Care Med. 1994 Jul;150(1):207-13. doi: 10.1164/ajrccm.150.1.7912987.
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Diagnosing bacterial respiratory infection by bronchoalveolar lavage.
J Infect Dis. 1987 May;155(5):862-9. doi: 10.1093/infdis/155.5.862.
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Early bacteriologic, immunologic, and clinical courses of young infants with cystic fibrosis identified by neonatal screening.通过新生儿筛查确诊的囊性纤维化幼儿的早期细菌学、免疫学和临床病程。
J Pediatr. 1991 Aug;119(2):211-7. doi: 10.1016/s0022-3476(05)80729-2.
5
Predictive value of oropharyngeal cultures for identifying lower airway bacteria in cystic fibrosis patients.口咽培养对囊性纤维化患者下呼吸道细菌的识别预测价值。
Am Rev Respir Dis. 1991 Aug;144(2):331-7. doi: 10.1164/ajrccm/144.2.331.
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