Ground glass and fibrotic change in children with surfactant protein C dysfunction mutations-Reference-Cited by-同舟云学术

Ground glass and fibrotic change in children with surfactant protein C dysfunction mutations

Published:2021-05-11 Issue:7 Volume:56 Page:2223-2231
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatric Pulmonology

Author:

DeBoer Emily M.¹²^ORCID,Liptzin Deborah R.¹²^ORCID,Humphries Stephen M.³,Lynch David A.³,Robison Kyle²,Galambos Csaba²⁴,Dishop Megan K.¹²⁵,Deterding Robin R.¹²,Weinman Jason P.²⁶

Affiliation:

1. Department of Pediatrics University of Colorado Anschutz Medical Campus Aurora Colorado USA

2. Breathing Institute Children's Hospital Colorado Aurora Colorado USA

3. Department of Radiology National Jewish Health Denver Colorado USA

4. Department of Pathology and Laboratory Medicine University of Colorado Anschutz Medical Campus Aurora Colorado USA

5. Department of Pathology University of Arizona Phoenix Arizona USA

6. Department of Radiology University of Colorado Anschutz Medical Campus and Children's Hospital Colorado Aurora Colorado USA

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ppul.25356

Reference40 articles.

1. Surfactant Dysfunction Mutations in Children's Interstitial Lung Disease and Beyond

2. A Mutation in the Surfactant Protein C Gene Associated with Familial Interstitial Lung Disease

3. Heterozygosity for a Surfactant Protein C Gene Mutation Associated with Usual Interstitial Pneumonitis and Cellular Nonspecific Interstitial Pneumonitis in One Kindred

4. Familial interstitial disease with I73T mutation: A mid- and long-term study

5. Variable phenotype associated with SP-C gene mutations: fatal case with the I73T mutation

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