Associate Professor of Medicine, University Iowa College of Medicine
Gastroenterology
Dr. David E. Elliott, MD
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Doctor David E. Elliott, MD works in the field of Gastroenterology. He attended Wayne State University School of Medicine. Wayne State University School of Medicine has a rank of 63 in research and a 85 in primary care David E. Elliott, MD has written publications. He has 32 publications published with PubMed. The lastest paper is: 'Intestinal Helminths Regulate Lethal Acute Graft-versus-Host Disease and Preserve the Graft-versus-Tumor Effect in Mice.' He accepts Medicare payments and is listed with Medicare.gov.
Publications
- Intestinal Helminths Regulate Lethal Acute Graft-versus-Host Disease and Preserve the Graft-versus-Tumor Effect in Mice.
- Helminth Infections Decrease Host Susceptibility to Immune-Mediated Diseases.
- Innate Immunity in Disease.
- Randomised clinical trial: the safety and tolerability of Trichuris suis ova in patients with Crohn's Disease.
- Translatability of helminth therapy in inflammatory bowel Diseases.
- Nematode Asparaginyl-tRNA Synthetase Resolves Intestinal Inflammation in Mice with T-Cell Transfer Colitis.
- Where are we on worms?
- Helminth-host immunological interactions: prevention and control of immune-mediated Diseases.
- Trichuris suis might be effective in treating allergic rhinitis.
- Advances in the pathogenesis and treatment of IBD.
- Helminths and the IBD hygiene hypothesis.
- Helminthic therapy: using worms to treat immune-mediated Disease.
- Colonization with Heligmosomoides polygyrus suppresses mucosal IL-17 production.
- Heligmosomoides polygyrus promotes regulatory T-cell cytokine production in the murine normal distal intestine.
- Immunologic and molecular mechanisms in inflammatory bowel Disease.
- Therapeutic colonization with Trichuris suis.
- Induction of CD8+ regulatory T cells in the intestine by Heligmosomoides polygyrus infection.
- Intestinal helminths protect in a murine model of asthma.
- Heligmosomoides polygyrus induces TLR4 on murine mucosal T cells that produce TGFbeta after lipopolysaccharide stimulation.
- Why Trichuris suis should prove safe for use in inflammatory bowel Diseases.
- Trichuris suis therapy for active Ulcerative colitis: a randomized controlled trial.
- IL-12 induction of mRNA encoding substance P in murine macrophages from the spleen and sites of inflammation.
- Helminths and the modulation of mucosal inflammation.
- CD4+ T cells from IL-10-deficient mice transfer susceptibility to NSAID-induced Rag colitis.
- Cutting edge: hemokinin has substance P-like function and expression in inflammation.
- Trichuris suis seems to be safe and possibly effective in the treatment of inflammatory bowel Disease.
- Exposure to schistosome eggs protects mice from TNBS-induced colitis.
- T cell substance P receptor governs antigen-elicited IFN-gamma production.
- Interleukin-4 receptor alpha chain and STAT6 signaling inhibit gamma interferon but not Th2 cytokine expression within schistosome granulomas.
- IL-4 inhibits vasoactive Intestinal peptide production by macrophages.
- The possible link between de-worming and the emergence of immunological Disease.
Schools
Wayne State University School Of Medicine
Johns Hopkins Hospital
University Iowa Hosps
Procedures Preformed
- Anoscopy
- Colonoscopy, Proctosigmoidoscopy, and Sigmoidoscopy
- Endoscopy (Esophagus, Stomach, Small Intestine)
Conditions Treated
- Abdominal Pain
- Anemia
- Barrett's Esophagus
- Benign Neoplasm of the Digestive System
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Doctors Specialties
- Gastroenterology
Accepted Insurances
Education
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University of Iowa Hospitals and Clinics -
Johns Hopkins University -
Wayne State University School of Medicine
Drug Facts
| NPI NUMBER | 1881668689 | |
| NPPES Provider LastName | ELLIOTT | |
| NPPES Provider FirstName | DAVID | |
| NPPES Provider ZIPCode | 522421009 | |
| NPPES Provider State | IA | |
| Specialty Description | Gastroenterology | |
| Total Claim Count | 561.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1881668689 |
| Last Name Of The Provider | ELLIOTT |
| First Name Of The Provider | DAVID |
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