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EDWARD PEARSON, M.D. , ABIHM
M.D. , ABIHM
General Practice Physician
NPI: 1306913876IndividualAccepts Medicare
Specialties, Licenses & Credentials
General Practice PhysicianPrimary
General Practice
Code: 208D00000X
ME83846(FL)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
UNIVERSITY OF SOUTH FLORIDA COLLEGE OF MEDICINE
Class of 1999
Research & Publications (20)
Historical approaches to the treatment of Adductor-Type Spasmodic Dysphonia (ADSD): review and tutorial.
PMID 14757929·NeuroRehabilitation·2003
6-review
A reappraisal of the clinical spectrum of North Carolina macular dystrophy.
PMID 19616854·Ophthalmology·2009
8-other
Pharmacogenetics and future strategies in treating hyperglycaemia in diabetes.
PMID 19273354·Front Biosci (Landmark Ed)·2009
6-review
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
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
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
Laparoscopic treatment of celiac artery compression syndrome: case series and review of current treatment modalities.
PMID 18818978·J Gastrointest Surg·2009
5-case
Comfort and its measurement--a literature review.
PMID 19565373·Disabil Rehabil Assist Technol·2009
6-review
Reduced-function SLC22A1 polymorphisms encoding organic cation transporter 1 and glycemic response to metformin: a GoDARTS study.
PMID 19336679·Diabetes·2009
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
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
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
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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1201 US HIGHWAY 1, SUITE 46
N PALM BEACH, FL 33408 - Phone
- (561) 290-4325
Quick Facts
- NPI
- 1306913876
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 27
- Publications
- 20
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