Current state of the art MRI for the longitudinal assessment of cystic fibrosis-Reference-Cited by-同舟云学术

Current state of the art MRI for the longitudinal assessment of cystic fibrosis

Published:2019-12-17 Issue:5 Volume:52 Page:1306-1320
ISSN:1053-1807
Container-title:Journal of Magnetic Resonance Imaging
language:en
Short-container-title:J Magn Reson Imaging

Author:

Woods Jason C.¹^ORCID,Wild Jim M.²,Wielpütz Mark O.³⁴,Clancy John P.¹,Hatabu Hiroto⁵,Kauczor Hans‐Ulrich³⁴,Beek Edwin J.R.⁶^ORCID,Altes Talissa A.⁷

Affiliation:

1. Center for Pulmonary Imaging Research, Division of Pulmonary Medicine and Department of Radiology Cincinnati Children's Hospital and University of Cincinnati Cincinnati Ohio USA

2. Department of Radiology University of Sheffield Sheffield UK

3. Department of Diagnostic and Interventional Radiology University of Heidelberg Heidelberg Germany

4. Translational Lung Research Center (TLRC) Heidelberg German Center for lung Research (DZL) Heidelberg Germany

5. Center for Pulmonary Functional Imaging, Department of Radiology Brigham and Women's Hospital and Harvard Medical School Boston Massachusetts USA

6. Edinburgh Imaging, Queen's Medical Research Institute University of Edinburgh Edinburgh UK

7. Department of Radiology University of Missouri Columbia Missouri USA

Funder

National Institutes of Health

Publisher

Wiley

Subject

Radiology, Nuclear Medicine and imaging

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jmri.27030

Reference107 articles.

1. Cystic Fibrosis and Its Management Through Established and Emerging Therapies

2. Efficacy and safety of lumacaftor and ivacaftor in patients aged 6–11 years with cystic fibrosis homozygous for F508del-CFTR : a randomised, placebo-controlled phase 3 trial

3. Physiologic endpoints for clinical studies for cystic fibrosis

4. Lumacaftor/Ivacaftor in Patients Aged 6–11 Years with Cystic Fibrosis and Homozygous forF508del-CFTR

5. Assessment of clinical response to ivacaftor with lung clearance index in cystic fibrosis patients with a G551D- CFTR mutation and preserved spirometry: a randomised controlled trial

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