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DR. THOMAS HARRY WEBB III M.D.
M.D.
Vascular Surgery Physician
NPI: 1093795528IndividualAccepts Medicare
Specialties, Licenses & Credentials
Vascular Surgery PhysicianPrimary
Surgery — Vascular Surgery
Code: 2086S0129X
21517(NE)33729(IA)01074731A(IN)
Education
VIRGINIA COMMONWEALTH UNIVERSITY, SCHOOL OF MEDICINE
Class of 1984
Research & Publications (20)
Inhibition of CD1d1-mediated antigen presentation by the vaccinia virus B1R and H5R molecules.
PMID 16981180·Eur J Immunol·2006
7-preclinical
Media literacy as a violence-prevention strategy: a pilot evaluation.
PMID 19182263·Health Promot Pract·2010
3-trial
Age of onset and death in inherited prion disease are heritable.
PMID 18729123·Am J Med Genet B Neuropsychiatr Genet·2009
8-other
Distinct melanocortin 2 receptor accessory protein domains are required for melanocortin 2 receptor interaction and promotion of receptor trafficking.
PMID 18818285·Endocrinology·2009
7-preclinical
Protected block curriculum enhances learning during general surgery residency training.
PMID 19221328·Arch Surg·2009
8-other
Seven-year discordance in age at onset in monozygotic twins with inherited prion disease (P102L).
PMID 19207267·Neuropathol Appl Neurobiol·2009
5-case
Ex vivo induction and expansion of natural killer T cells by CD1d1-Ig coated artificial antigen presenting cells.
PMID 19446558·J Immunol Methods·2009
7-preclinical
Antipsychotic treatment of first-episode or early-onset schizophrenia.
PMID 19635232·Curr Psychiatry Rep·2009
8-other
Generation of new synthetic scaffolds using framework libraries selected and refined via medicinal chemist synthetic expertise.
PMID 18335978·J Chem Inf Model·2008
8-other
Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal development.
PMID 18765564·J Cell Sci·2008
7-preclinical
Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series.
PMID 18757886·Brain·2008
8-other
Ascites specific inhibition of CD1d-mediated activation of natural killer T cells.
PMID 19047090·Clin Cancer Res·2008
7-preclinical
In search of the psychosis gene in people with Prader-Willi syndrome.
PMID 18324689·Am J Med Genet A·2008
8-other
First report of Creutzfeldt-Jakob disease occurring in 2 siblings unexplained by PRNP mutation.
PMID 18716560·J Neuropathol Exp Neurol·2008
5-case
Only half right: species with female-biased sexual size dimorphism consistently break Rensch's rule.
PMID 17878932·PLoS One·2007
7-preclinical
Violent entertainment pitched to adolescents: an analysis of PG-13 films.
PMID 17545355·Pediatrics·2007
4-observational
Analysis of candidate imprinted genes in PWS subjects with atypical genetics: a possible inactivating mutation in the SNURF/SNRPN minimal promoter.
PMID 17262171·J Hum Genet·2007
8-other
CD36 expression and its relationship with obesity in blood cells from people with and without Prader-Willi syndrome.
PMID 16451133·Clin Genet·2006
4-observational
Does changing behavioral intentions engender behavior change? A meta-analysis of the experimental evidence.
PMID 16536643·Psychol Bull·2006
1-meta
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 5255 E STOP 11 RD STE 200
INDIANAPOLIS, IN 46237 - Phone
- (317) 851-2331
Quick Facts
- NPI
- 1093795528
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 2
- Years in Practice
- 42
- Publications
- 20
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