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首页> Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society> CFTR-function and ventilation inhomogeneity in individuals with cystic fibrosis.

CFTR-function and ventilation inhomogeneity in individuals with cystic fibrosis.

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第一作者： Nadine,Bernasconi

第一单位： Division of Respiratory Medicine, University Children's Hospital of Zurich, Zurich, Switzerland.

作者： Nadine,Bernasconi ^[1] ; Elisabeth,Kieninger ^[2] ; Michelle,Shaw ^[3] ; Johanna,Kurz ^[2] ; Alexander,Moeller ^[1] ; Felix,Ratjen ^[3] ; Isabelle,Rochat ^[4] ; Sanja,Stanojevic ^[3] ; Florian,Singer ^[5]

作者单位： Division of Respiratory Medicine, University Children's Hospital of Zurich, Zurich, Switzerland. ^[1] Pediatric Respiratory Medicine, Department of Pediatrics, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland. ^[2] Division of Respiratory Medicine, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Canada. ^[3] Pediatric Pulmonology Unit, Department of Pediatrics, CHUV Lausanne, University Hospital of Lausanne, Switzerland. ^[4] Pediatric Respiratory Medicine, Department of Pediatrics, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland. Electronic address: florian.singer@insel.ch. ^[5]

关键词 Child Cystic fibrosis Pulmonary function Treatment

主题词青少年(Adolescent);儿童(Child);儿童, 学龄前(Child, Preschool);横断面研究(Cross-Sectional Studies);囊性纤维化(Cystic Fibrosis);囊性纤维化跨膜传导调节因子(Cystic Fibrosis Transmembrane Conductance Regulator);女(雌)性(Female);人类(Humans);男(雄)性(Male);肺通气(Pulmonary Ventilation);呼吸功能试验(Respiratory Function Tests);回顾性研究(Retrospective Studies)

DOI 10.1016/j.jcf.2020.12.009

PMID 33349584

发布时间 2022-01-28

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Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Journal of cystic fibrosis

2021年20卷4期

641-647页

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