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EDWARD PEARSON, MD
MD
Hematology & Oncology Physician
NPI: 1801188172IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
P9241(TX)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Hematology & Oncology PhysicianPrimary
Internal Medicine — Hematology & Oncology
Code: 207RH0003X
P9241(TX)
Education
TEXAS A & M UNIVERSITY SYSTEM, HSC, COLLEGE OF MEDICINE
Class of 2011
Research & Publications (20)
Comfort and its measurement--a literature review.
PMID 19565373·Disabil Rehabil Assist Technol·2009
6-review
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
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
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
A reappraisal of the clinical spectrum of North Carolina macular dystrophy.
PMID 19616854·Ophthalmology·2009
8-other
Reduced-function SLC22A1 polymorphisms encoding organic cation transporter 1 and glycemic response to metformin: a GoDARTS study.
PMID 19336679·Diabetes·2009
8-other
Pharmacogenetics and future strategies in treating hyperglycaemia in diabetes.
PMID 19273354·Front Biosci (Landmark Ed)·2009
6-review
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
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
Surface modification of microspheres with steric stabilizing and cationic polymers for gene delivery.
PMID 18558783·Langmuir·2008
8-other
10q26 is associated with increased risk of age-related macular degeneration in the Utah population.
PMID 18188952·Adv Exp Med Biol·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
Association of HTRA1 polymorphism and bilaterality in advanced age-related macular degeneration.
PMID 18206206·Vision Res·2008
8-other
Toll-like receptor 3 and geographic atrophy in age-related macular degeneration.
PMID 18753640·N Engl J Med·2008
4-observational
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
- 3535 Worth St, Suite C-1025
Dallas, TX 75246 - Phone
- (214) 885-1020
Quick Facts
- NPI
- 1801188172
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 2
- Years in Practice
- 15
- Publications
- 20
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