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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816451PMC
http://dx.doi.org/10.5213/inj.2142204.102DOI Listing

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Article Synopsis
  • Familial Pulmonary Fibrosis (FPF) is a lung disease caused by genetic mutations, and managing it is still a challenge as of 2023.
  • A survey conducted in Italy found that more FPF patients are seen at hospitals that treat many interstitial lung disease (ILD) patients each year.
  • There were differences in genetic testing services between hospitals, but no major differences in patient care or treatments were found in various medical settings.
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Reply to Ni : Comprehensive Strategies for the Follow-Up of Interstitial Lung Abnormality.

Am J Respir Crit Care Med

September 2024

Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.

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