Back to Search
MICHAEL CONLEY MD
MD
Pulmonary Disease Physician
NPI: 1194105601IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
35.132771(OH)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Pulmonary Disease PhysicianPrimary
Internal Medicine — Pulmonary Disease
Code: 207RP1001X
35.132771(OH)
Education
OTHER
Class of 2015
Research & Publications (20)
Genetics of hypogammaglobulinemia: what do we really know?
PMID 19651503·Curr Opin Immunol·2009
6-review
Uncoupling protein 2 polymorphisms as risk factors for NTDs.
PMID 19137581·Birth Defects Res A Clin Mol Teratol·2009
8-other
Genetic and demographic features of X-linked agammaglobulinemia in Eastern and Central Europe: a cohort study.
PMID 19419768·Mol Immunol·2009
8-other
Primary B cell immunodeficiencies: comparisons and contrasts.
PMID 19302039·Annu Rev Immunol·2009
4-observational
An infant with erythroderma, skin scaling, chronic emesis, and intractable diarrhea.
PMID 18832538·Clin Pediatr (Phila)·2009
5-case
A minimally hypomorphic mutation in Btk resulting in reduced B cell numbers but no clinical disease.
PMID 18241230·Clin Exp Immunol·2008
5-case
Eye malformations in children with heavy alcohol exposure in utero.
PMID 18571671·J Pediatr·2008
4-observational
Folate-related gene polymorphisms as risk factors for cleft lip and cleft palate.
PMID 18661527·Birth Defects Res A Clin Mol Teratol·2008
4-observational
Adults with X-linked agammaglobulinemia: impact of disease on daily lives, quality of life, educational and socioeconomic status, knowledge of inheritance, and reproductive attitudes.
PMID 18794707·Medicine (Baltimore)·2008
8-other
Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population.
PMID 18798306·Am J Med Genet A·2008
8-other
Gross deletions involving IGHM, BTK, or Artemis: a model for genomic lesions mediated by transposable elements.
PMID 18252213·Am J Hum Genet·2008
8-other
Markers of oxidative stress and systemic vasoconstriction in pregnant women drinking > or =48 g of alcohol per day.
PMID 18715278·Alcohol Clin Exp Res·2008
8-other
Abciximab-induced alveolar hemorrhage after percutaneous coronary intervention.
PMID 18273491·Can J Cardiol·2008
5-case
The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population.
PMID 17486595·Am J Med Genet A·2007
8-other
Cutting edge: a hypomorphic mutation in Igbeta (CD79b) in a patient with immunodeficiency and a leaky defect in B cell development.
PMID 17675462·J Immunol·2007
3-trial
Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee.
PMID 17952897·J Allergy Clin Immunol·2007
8-other
A possible bichromatid mutation in a male gamete giving rise to a female mosaic for two different mutations in the X-linked gene WAS.
PMID 17250667·Clin Genet·2007
5-case
Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee Meeting in Budapest, 2005.
PMID 16680902·J Allergy Clin Immunol·2006
8-other
Severe combined immunodeficiency associated with nephrogenic diabetes insipidus and a deletion in the Xq28 region.
PMID 16781893·Clin Immunol·2006
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via TRI-STATE PULMONARY ASSOCIATES, INC. · 3 locations total
- Address
- 2123 AUBURN AVE, SUITE 401
CINCINNATI, OH 45219 - Phone
- (513) 241-5489
Quick Facts
- NPI
- 1194105601
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 3
- Years in Practice
- 11
- Publications
- 20
Are you this provider?
Claim Your Profile