Associated Papers
Clinical characteristics of SFTPC gene mutations in children: a single-center experience.
Yang T et al.
Italian Journal of Pediatrics, 2025
40890883 (PubMed )
Supplement: 13052_2025_2101_MOESM3_ESM.doc
A comparative analysis of clinical phenotypes and outcomes in childhood interstitial lung disease due to surfactant dysfunction disorders: focusing on mutations in SFTPC, ABCA3, and NKX2-1 genes.
Tang X et al.
Italian Journal of Pediatrics, 2025
Genetic testing for rare pediatric lung disorders: The promise and the pitfalls.
Nogee LM
Pediatric Investigation, 2020
Surfactant protein C dysfunction with new clinical insights for diffuse alveolar hemorrhage and autoimmunity.
Tang X et al.
Pediatric Investigation, 2019
Genetic basis of surfactant dysfunction in Chinese children: A retrospective study.
Chen J et al.
Pediatric Pulmonology, 2019
Systematic review of drug effects in humans and models with surfactant-processing disease.
Klay D et al.
European Respiratory Review : an Official Journal of the European Respiratory Society, 2018
Genetic basis for childhood interstitial lung disease among Japanese infants and children.
Hayasaka I et al.
Pediatric Research, 2018
Recurrent diffuse lung disease due to surfactant protein C deficiency.
Kazzi B et al.
Respiratory Medicine Case Reports, 2018
[Clinical manifestations of three cases of surfactant protein C p. V39L mutation].
Chen JH et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2017
A novel surfactant protein C gene mutation associated with progressive respiratory failure in infancy.
Litao MK et al.
Pediatric Pulmonology, 2017
Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patients.
Kröner C et al.
The European Respiratory Journal, 2015
Natural history of five children with surfactant protein C mutations and interstitial lung disease.
Avital A et al.
Pediatric Pulmonology, 2014
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