Found: 7
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Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening.
- Published in:
- Nature Genetics, 2015, v. 47, n. 5, p. 512, doi. 10.1038/ng.3278
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- Publication type:
- Article
Race and Ethnicity in Pulmonary Function Test Interpretation: An Official American Thoracic Society Statement.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2023, v. 207, n. 8, p. 978, doi. 10.1164/rccm.202302-0310ST
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- Publication type:
- Article
Enhancing Recruitment and Retention of Minority Populations for Clinical Research in Pulmonary, Critical Care, and Sleep Medicine: An Official American Thoracic Society Research Statement: Executive Summary.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2021, v. 204, n. 3, p. 256, doi. 10.1164/rccm.202105-1210ST
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- Publication type:
- Article
Enhancing Recruitment and Retention of Minority Populations for Clinical Research in Pulmonary, Critical Care, and Sleep Medicine: An Official American Thoracic Society Research Statement.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Health Care Disparities in Pulmonary Fibrosis—Time to Move the Needle Forward.
- Published in:
- 2023
- By:
- Publication type:
- Opinion
Sarcoidosis Th17 Cells are ESAT-6 Antigen Specific but Demonstrate Reduced IFN-γ Expression.
- Published in:
- Journal of Clinical Immunology, 2013, v. 33, n. 2, p. 446, doi. 10.1007/s10875-012-9817-6
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- Publication type:
- Article
The Increasing Use of Social Media for Medical Information: Should Healthcare Providers Be Concerned?
- Published in:
- 2019
- By:
- Publication type:
- journal article