Back to Search
AARON SHIELS, M.D.
M.D.
Gastroenterology Physician
NPI: 1467448324IndividualAccepts Medicare
Specialties, Licenses & Credentials
Gastroenterology PhysicianPrimary
Internal Medicine — Gastroenterology
Code: 207RG0100X
36110865(IL)
Education
WASHINGTON UNIVERSITY SCHOOL OF MEDICINE
Class of 1997
Research & Publications (20)
Pharmacogenetics of complement factor H (Y402H) and treatment of exudative age-related macular degeneration with ranibizumab.
PMID 19091853·Br J Ophthalmol·2009
8-other
Association of complement factor H and LOC387715 genotypes with response of exudative age-related macular degeneration to photodynamic therapy.
PMID 18292785·Eye (Lond)·2009
8-other
The EPHA2 gene is associated with cataracts linked to chromosome 1p.
PMID 19005574·Mol Vis·2008
8-other
Vascular KCNQ potassium channels as novel targets for the control of mesenteric artery constriction by vasopressin, based on studies in single cells, pressurized arteries, and in vivo measurements of mesenteric vascular resistance.
PMID 18272810·J Pharmacol Exp Ther·2008
7-preclinical
Refractive defects and cataracts in mice lacking lens intrinsic membrane protein-2.
PMID 17251442·Invest Ophthalmol Vis Sci·2007
7-preclinical
Association of complement factor H and LOC387715 genotypes with response of exudative age-related macular degeneration to intravitreal bevacizumab.
PMID 18054635·Ophthalmology·2007
8-other
X-linked idiopathic infantile nystagmus associated with a missense mutation in FRMD7.
PMID 18087240·Mol Vis·2007
8-other
CHMP4B, a novel gene for autosomal dominant cataracts linked to chromosome 20q.
PMID 17701905·Am J Hum Genet·2007
7-preclinical
Clinical phenotypes associated with the complement factor H Y402H variant in age-related macular degeneration.
PMID 17631852·Am J Ophthalmol·2007
8-other
Successful endoscopic management of gastrojejunal anastomotic strictures after Roux-en-Y gastric bypass.
PMID 17451700·Gastrointest Endosc·2007
8-other
Regulation of aquaporin water permeability in the lens.
PMID 15790907·Invest Ophthalmol Vis Sci·2005
7-preclinical
A novel missense mutation in the gene for gap-junction protein alpha3 (GJA3) associated with autosomal dominant "nuclear punctate" cataracts linked to chromosome 13q.
PMID 15208569·Mol Vis·2004
8-other
Intravenous proton pump inhibitors: requiem for endoscopic therapy?
PMID 15057764·Gastroenterology·2004
8-other
A missense mutation in the gammaD crystallin gene (CRYGD) associated with autosomal dominant "coral-like" cataract linked to chromosome 2q.
PMID 15041957·Mol Vis·2004
8-other
Cell death triggered by a novel mutation in the alphaA-crystallin gene underlies autosomal dominant cataract linked to chromosome 21q.
PMID 14512969·Eur J Hum Genet·2003
8-other
Galactokinase gene mutations and age-related cataract. Lack of association in an Italian population.
PMID 12942049·Mol Vis·2003
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
- 401 ROXBURY RD
ROCKFORD, IL 61107 - Phone
- (815) 397-7340
Quick Facts
- NPI
- 1467448324
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 29
- Publications
- 20
Are you this provider?
Claim Your Profile