Michael Davenport, MD
Clinical Assistant Professor of Medicine (General Internal Medicine)
Attending, Corporal Michael J. Crescenz VA Medical Center
Department: Medicine
Contact information
Corporal Michael J. Crescenz VA Medical Center
3900 Woodland Ave
Philadelphia, PA 19104
3900 Woodland Ave
Philadelphia, PA 19104
Education:
BS (Biomedical Engineering with Cell & Tissue Engineering concentration )
John Hopkins University, 2009.
MD
New York University School of Medicine, 2014.
BS (Biomedical Engineering with Cell & Tissue Engineering concentration )
John Hopkins University, 2009.
MD
New York University School of Medicine, 2014.
Post-Graduate Training
Intern, Internal Medicine, Hospital of the University of Pennsylvania, 2014-2015.
Resident, Internal Medicine, Hospital of the University of Pennsylvania, 2015-2017.
Intern, Internal Medicine, Hospital of the University of Pennsylvania, 2014-2015.
Resident, Internal Medicine, Hospital of the University of Pennsylvania, 2015-2017.
Certifications
American Board of Internal Medicine, 2017.
Permanent linkAmerican Board of Internal Medicine, 2017.
Selected Publications
Day T, Davenport M, Keddem S, Garin M, Stankiewicz C, Burke R: Physician Perspectives on Hospitalist Co-Management on an Inpatient Psychiatry Unit. Society of General Internal Medicine 2020.Wong T, Dubin P, Davenport M, Bass G, Myers J, Wagner J.: A Quality Improvement Initiative Reduced Low-Value Red Blood Cell Transfusions in Hospitalized Oncology Patients. American Society of Clinical Oncology Quality Care Symposium, Orlando, Florida. 2017 Notes: Poster Presentation.
Tang MS, Poles J, Leung JM, Wolff MJ, Davenport M, Lee SC, Lim YA, Chua KH, Loke P, Cho I.: Inferred metagenomic comparison of mucosal and fecal microbiota from individuals undergoing routine screening colonoscopy reveal similar differences observed during active inflammation. Gut Microbes. 6(1): 48-56, 2015.
Davenport M, Poles J, Leung JM, Wolff MJ, Abidi WM, Ullman T, Mayer L, Cho I, Loke P.: Metabolic alterations to the mucosal microbiota in inflammatory bowel disease. Inflamm Bowel Dis. 20(4): 723-731, April 2014 Notes: doi: 10.1097/MIB.0000000000000011.
Leung JM, Davenport M, Wolff MJ, Wiens K, Abidi W, Poles MA, Cho I, Ullman T, Mayer L, Loke P.: IL-22 producing CD4+ cells are depleted in actively inflamed colitis tissue. Mucosal Immunol. 7(1): 124-133, Jan 2014 Notes: doi: 10.1038/mi.2013.31.
Davenport M.: Metabolic alterations to the mucosal microbiota of inflammatory bowel disease patients are associated with CD4+ T cell homeostasis. Crohns & Colitis Foundation of America Advances in Inflammatory Bowel Diseases conference, Hollywood, Florida. 2013 Notes: Poster presentation.
Leung JM, Cho I, Davenport M, Wolff MJ, Ullman TA, Poles MA, Mayer L, Loke P.: A population of cytokine deficient CD4+ T cells is associated with increased body mass and intestinal inflammation. Digestive Disease Week, San Diego, California May 2012 Notes: Poster Presentation.
Wolff MJ, Leung JM, Davenport M, Cho I, Poles MA, Loke P.: TH17 and FoxP3+ cells are enriched in the healthy human cecum. Digestive Disease Week, San Diego, California. May 2012 Notes: Poster Presentation.
Wolff MJ, Leung JM, Davenport M, Cho I, Poles MA, Loke P.: TH17, TH22, and FoxP3+ cells are enriched in the healthy human cecum. New York Society for Gastrointestinal Endoscopy (NYSGE) Annual New York Course, New York, New York. 2012 Notes: Poster Presentation.
Wolff MJ, Leung JM, Davenport M, Poles MA, Cho I, Loke P.: TH17, TH22 and TReg Cells Are Enriched in the Healthy Human Cecum. PLoS ONE. 7(7): e41373, 2012 Notes: doi: 10.1371/journal.pone.0041373.