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MARGARET SIMPSON, M.D.
M.D.
Family Medicine Physician
NPI: 1225081664IndividualAccepts Medicare
Specialties, Licenses & Credentials
CMS Specialties
PrimaryFAMILY PRACTICE
Education
OTHER
Class of 1987
Research & Publications (20)
Lethal cystic kidney disease in Amish neonates associated with homozygous nonsense mutation of NPHP3.
PMID 19303681·Am J Kidney Dis·2009
4-observational
Homozygous mutation of desmocollin-2 in arrhythmogenic right ventricular cardiomyopathy with mild palmoplantar keratoderma and woolly hair.
PMID 18957847·Cardiology·2009
5-case
A mutation in NFkappaB interacting protein 1 causes cardiomyopathy and woolly haircoat syndrome of Poll Hereford cattle.
PMID 19016676·Anim Genet·2009
7-preclinical
1H and 19F nuclear magnetic resonance microimaging of water and chemical distribution in soil columns.
PMID 17665672·Environ Toxicol Chem·2007
8-other
Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development.
PMID 17924334·Am J Hum Genet·2007
7-preclinical
Cell-free synthetic biology: a bottom-up approach to discovery by design.
PMID 17170764·Mol Syst Biol·2006
8-other
Increased abundance of labile intracellular zinc during cell proliferation was due to increased retention of extracellular zinc in 3T3 cells.
PMID 16443356·J Nutr Biochem·2006
7-preclinical
Identification of mobile aliphatic sorptive domains in soil humin by solid-state 13C nuclear magnetic resonance.
PMID 16494224·Environ Toxicol Chem·2006
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
- 621 S MAIN ST, SUITE 201
REIDSVILLE, NC 27320 - Phone
- (336) 348-6924
Quick Facts
- NPI
- 1225081664
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 39
- Publications
- 20
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