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DAWN DEMEO, MD
MD
Pulmonary Disease Physician
NPI: 1346206588Individual
Specialties, Licenses & Credentials
Pulmonary Disease PhysicianPrimary
Internal Medicine — Pulmonary Disease
Code: 207RP1001X
155912(MA)
Research & Publications (20)
Heritability of lung function in severe alpha-1 antitrypsin deficiency.
PMID 18931508·Hum Hered·2009
4-observational
IL10 polymorphisms are associated with airflow obstruction in severe alpha1-antitrypsin deficiency.
PMID 17690329·Am J Respir Cell Mol Biol·2008
4-observational
Genetic determinants of emphysema distribution in the national emphysema treatment trial.
PMID 17363767·Am J Respir Crit Care Med·2007
4-observational
Determinants of airflow obstruction in severe alpha-1-antitrypsin deficiency.
PMID 17389752·Thorax·2007
4-observational
The SERPINE2 gene is associated with chronic obstructive pulmonary disease.
PMID 16921128·Proc Am Thorac Soc·2006
7-preclinical
The SERPINE2 gene is associated with chronic obstructive pulmonary disease.
PMID 16358219·Am J Hum Genet·2006
7-preclinical
Concordance of genotypes in pre- and post-lung transplantation DNA samples.
PMID 15994430·Am J Respir Cell Mol Biol·2005
8-other
Alpha1-antitrypsin deficiency. 2: genetic aspects of alpha(1)-antitrypsin deficiency: phenotypes and genetic modifiers of emphysema risk.
PMID 14985567·Thorax·2004
6-review
Familial aggregation of FEF(25-75) and FEF(25-75)/FVC in families with severe, early onset COPD.
PMID 15115866·Thorax·2004
8-other
Genome-wide linkage of forced mid-expiratory flow in chronic obstructive pulmonary disease.
PMID 15347563·Am J Respir Crit Care Med·2004
8-other
Genetics of chronic obstructive pulmonary disease.
PMID 16088534·Semin Respir Crit Care Med·2003
8-other
Univariate and multivariate family-based association analysis of the IL-13 ARG130GLN polymorphism in the Childhood Asthma Management Program.
PMID 12432502·Genet Epidemiol·2002
8-other
Associations of IL6 polymorphisms with lung function decline and COPD.
PMID 19359268·Thorax·2009
8-other
Molecular biomarkers for quantitative and discrete COPD phenotypes.
PMID 18849563·Am J Respir Cell Mol Biol·2009
8-other
Genetic association analysis of COPD candidate genes with bronchodilator responsiveness.
PMID 19111454·Respir Med·2009
8-other
National Emphysema Treatment Trial state of the art: genetics of emphysema.
PMID 18453360·Proc Am Thorac Soc·2008
6-review
Polymorphic variation in surfactant protein B is associated with COPD exacerbations.
PMID 18550614·Eur Respir J·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 15 FRANCIS ST, PBB LOBBY
BOSTON, MA 02115 - Phone
- (617) 732-6038
Quick Facts
- NPI
- 1346206588
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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