Back to Search
MICHAEL CONLEY, MD
MD
Specialist
NPI: 1962402750Individual
Specialties, Licenses & Credentials
SpecialistPrimary
Specialist
Code: 174400000X
MC039019(MI)
Research & Publications (20)
Uncoupling protein 2 polymorphisms as risk factors for NTDs.
PMID 19137581·Birth Defects Res A Clin Mol Teratol·2009
8-other
Primary B cell immunodeficiencies: comparisons and contrasts.
PMID 19302039·Annu Rev Immunol·2009
4-observational
Genetic and demographic features of X-linked agammaglobulinemia in Eastern and Central Europe: a cohort study.
PMID 19419768·Mol Immunol·2009
8-other
Genetics of hypogammaglobulinemia: what do we really know?
PMID 19651503·Curr Opin Immunol·2009
6-review
An infant with erythroderma, skin scaling, chronic emesis, and intractable diarrhea.
PMID 18832538·Clin Pediatr (Phila)·2009
5-case
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
A minimally hypomorphic mutation in Btk resulting in reduced B cell numbers but no clinical disease.
PMID 18241230·Clin Exp Immunol·2008
5-case
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
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
Eye malformations in children with heavy alcohol exposure in utero.
PMID 18571671·J Pediatr·2008
4-observational
Abciximab-induced alveolar hemorrhage after percutaneous coronary intervention.
PMID 18273491·Can J Cardiol·2008
5-case
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
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
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
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
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
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
A peptide zipcode sufficient for anterograde transport within amyloid precursor protein.
PMID 17062754·Proc Natl Acad Sci U S A·2006
7-preclinical
Au- and pt-catalyzed cycloisomerizations of 1,5-enynes to cyclohexadienes with a broad alkyne scope.
PMID 16866525·J Am Chem Soc·2006
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
- 1414 W FAIR AVE, SUITE 247
MARQUETTE, MI 49855 - Phone
- (906) 225-4480
Quick Facts
- NPI
- 1962402750
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile