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Lung deposition of inhaled Alpha-1-proteinase inhibitor (Alpha1-PI) - problems and experience of Alpha1-PI inhalation therapy in patients with hereditary Alpha1-PI deficiency and cystic fibrosis

机译：吸入α-1蛋白酶抑制剂（α1-PI）的肺部沉积 - 遗传α1-PI缺乏症患者α1-PI吸入治疗的问题及体验及囊性纤维化

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R. Siekmeier;
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年度 2010
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1. Lung deposition of inhaled Alpha-1-proteinase inhibitor (Alpha₁-PI) - problems and experience of Alpha₁-PI inhalation therapy in patients with hereditary Alpha₁-PI deficiency and cystic fibrosis [J] . R Siekmeier European journal of medical research. . 2010,第Suppla2期

机译：吸入的Alpha-1-蛋白酶抑制剂（Alpha _{1 -PI）的肺沉积-遗传性Alpha _{1患者吸入Alpha _{1 -PI的问题和体会 -PI缺乏症和囊性纤维化}}}
2. Lung deposition of inhaled alpha1-proteinase inhibitor in cystic fibrosis and alpha1-antitrypsin deficiency. [J] . Brand P, Schulte M, Wencker M The European respiratory journal : . 2009,第2期

机译：吸入性α1-蛋白酶抑制剂的肺沉积在囊性纤维化和α1-抗胰蛋白酶缺乏症中。
3. Lung deposition of inhaled α1-proteinase inhibitor in cystic fibrosis and α1-antitrypsin deficiency [J] . C. H. Herpich, G. Klein, K. Hanna, The European respiratory journal : . 2009,第2期

机译：吸入性α1-蛋白酶抑制剂的肺沉积在囊性纤维化和α1-抗胰蛋白酶缺乏症中的作用
4. Dry powder inhalable bacteriophage-polymeric particles reduce lung cystic fibrosis bacterial infections [C] . Rachit Aaarwal, Christopher Johnson, Barry Imhoff, Society for Biomaterials annual meeting and exposition . 2017

机译：干粉吸入性噬菌体多聚颗粒减少肺囊性纤维化细菌感染
5. The effects of biofeedback-assisted breathing retraining on lung functions in patients with cystic fibrosis. [D] . Delk, Kerry K. 1989

机译：生物反馈辅助呼吸训练对囊性纤维化患者肺功能的影响。
6. Lung deposition of inhaled Alpha-1-proteinase inhibitor (Alpha1-PI) - problems and experience of Alpha1-PI inhalation therapy in patients with hereditary Alpha1-PI deficiency and cystic fibrosis [O] . R Siekmeier 2010

机译：吸入的Alpha-1-蛋白酶抑制剂（Alpha1-PI）的肺沉积-遗传性Alpha1-PI缺乏症和囊性纤维化患者的Alpha1-PI吸入疗法存在的问题和经验
7. Screening for alpha1-Pi deficiency in patients with lung diseases [O] . WENCKER M. 2000

机译：肺部疾病患者α1-Pi缺乏症的筛查

Lung deposition of inhaled Alpha-1-proteinase inhibitor (Alpha1-PI) - problems and experience of Alpha1-PI inhalation therapy in patients with hereditary Alpha1-PI deficiency and cystic fibrosis

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