Genetic Interstitial Lung Disease

2011/12/10 by Megan Devine, Megan Stuebner Devine, Christine Kim Garcia · 43 citations
Medicine · #Disease #Intensive care medicine #Internal medicine #Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis #Interstitial lung disease #Lung #Lung disease #Medical Imaging and Pathology Studies #Medicine #Neonatal Respiratory Health Research #Parenchyma #Pathology #Population #Pulmonologists

paper · doi:10.1016/j.ccm.2011.11.001

published in Clinics in Chest Medicine 33(1), 95-110 (Elsevier BV)

openalex publication_date 2011/12/10 · crossref created 2011/12/10 · crossref issued 2012/03/01 · crossref published 2012/03/01 · crossref published-print 2012/03/01 · crossref deposited 2025/10/03 · openalex created_date 2025/10/10 · crossref indexed 2026/01/15 · openalex updated_date 2026/07/23

Citations

• A Prospective, Cross-sectional Survey Study of the Natural History of Niemann-Pick Disease Type B
• Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita
• TINF2, a Component of the Shelterin Telomere Protection Complex, Is Mutated in Dyskeratosis Congenita
• Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita

Cited by

• Birt–Hogg–Dubé syndrome [wikipedia]