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ERIC PEARSON, DO
DO
Family Medicine Physician
NPI: 1336880954IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
5101028327(MI)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
MICHIGAN STATE UNIVERSITY COLLEGE OF OSTEOPATHIC MEDICINE
Class of 2022
Research & Publications (20)
Controlling cis/trans-selectivity in intramolecular Diels-Alder reactions of benzo-tethered, ester linked 1,3,9-decatrienes.
PMID 18219422·Org Biomol Chem·2008
8-other
Intramolecular Diels-Alder reactions of ester linked 1,3,9-decatrienes: cis/trans selectivity in thermal and Lewis acid promoted reactions of ethylene-tethered and benzo-tethered systems.
PMID 16872192·J Org Chem·2006
8-other
Pharmacogenetics and future strategies in treating hyperglycaemia in diabetes.
PMID 19273354·Front Biosci (Landmark Ed)·2009
6-review
Laparoscopic treatment of celiac artery compression syndrome: case series and review of current treatment modalities.
PMID 18818978·J Gastrointest Surg·2009
5-case
Reduced-function SLC22A1 polymorphisms encoding organic cation transporter 1 and glycemic response to metformin: a GoDARTS study.
PMID 19336679·Diabetes·2009
8-other
Adherence in patients transferred from immediate release metformin to a sustained release formulation: a population-based study.
PMID 19267712·Diabetes Obes Metab·2009
4-observational
Comfort and its measurement--a literature review.
PMID 19565373·Disabil Rehabil Assist Technol·2009
6-review
Region-of-interest image reconstruction with intensity weighting in circular cone-beam CT for image-guided radiation therapy.
PMID 19472624·Med Phys·2009
8-other
A reappraisal of the clinical spectrum of North Carolina macular dystrophy.
PMID 19616854·Ophthalmology·2009
8-other
Transition from insulin to sulfonylurea in a child with diabetes due to a mutation in KCNJ11 encoding Kir6.2--initial and long-term response to sulfonylurea therapy.
PMID 18548275·Eur J Pediatr·2009
5-case
Surface modification of microspheres with steric stabilizing and cationic polymers for gene delivery.
PMID 18558783·Langmuir·2008
8-other
Toll-like receptor 3 and geographic atrophy in age-related macular degeneration.
PMID 18753640·N Engl J Med·2008
4-observational
Association of HTRA1 polymorphism and bilaterality in advanced age-related macular degeneration.
PMID 18206206·Vision Res·2008
8-other
Genetic association of LOXL1 gene variants and exfoliation glaucoma in a Utah cohort.
PMID 18287813·Cell Cycle·2008
4-observational
Promoter polymorphism of the erythropoietin gene in severe diabetic eye and kidney complications.
PMID 18458324·Proc Natl Acad Sci U S A·2008
7-preclinical
A mutation (R826W) in nucleotide-binding domain 1 of ABCC8 reduces ATPase activity and causes transient neonatal diabetes.
PMID 18497752·EMBO Rep·2008
8-other
Glibenclamide unresponsiveness in a Brazilian child with permanent neonatal diabetes mellitus and DEND syndrome due to a C166Y mutation in KCNJ11 (Kir6.2) gene.
PMID 19169493·Arq Bras Endocrinol Metabol·2008
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 215 E MANSION ST STE 1E
MARSHALL, MI 49068 - Phone
- (269) 781-3938
Quick Facts
- NPI
- 1336880954
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 4
- Publications
- 20
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