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MARY LOR, PHARMD
PHARMD
Pharmacist
NPI: 1437455672Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
27282(NC)
Research & Publications (13)
Uncertainty during anticipation modulates neural responses to aversion in human insula and amygdala.
PMID 19679543·Cereb Cortex·2010
8-other
Comparative bioequivalence study between a novel matrix transdermal delivery system of fentanyl and a commercially available reservoir formulation.
PMID 16939522·Br J Clin Pharmacol·2007
2-rct
Characteristics of children's agricultural tasks in Hmong farming communities.
PMID 19274904·J Agromedicine·2006
8-other
Pharmacokinetics, tolerability, and performance of a novel matrix transdermal delivery system of fentanyl relative to the commercially available reservoir formulation in healthy subjects.
PMID 16707411·J Clin Pharmacol·2006
2-rct
Electron transfer at the single-molecule level in a triphenylamine-perylene imide molecule.
PMID 15884080·Chemphyschem·2005
8-other
Photophysical study of photoinduced electron transfer in a bis-thiophene substituted peryleneimide.
PMID 15616693·Photochem Photobiol Sci·2005
8-other
Probing the influence of O2 on photoinduced reversible electron transfer in perylenediimide-triphenylamine-based dendrimers by single-molecule spectroscopy.
PMID 15549754·Angew Chem Int Ed Engl·2004
8-other
Generation dependent singlet-singlet annihilation within multichromophoric dendrimers studied by polychromatic transient absorption.
PMID 14690223·Photochem Photobiol Sci·2003
8-other
Direct proof of electron transfer in a rigid first generation triphenyl amine core dendrimer substituted with a peryleneimide acceptor.
PMID 12803072·Photochem Photobiol Sci·2003
8-other
Energy transfer within perylene-terrylene dendrimers evidenced by polychromatic transient absorption measurements.
PMID 12713215·Photochem Photobiol Sci·2003
8-other
Photoinduced electron transfer in a rigid first generation triphenylamine core dendrimer substituted with a peryleneimide acceptor.
PMID 12175254·J Am Chem Soc·2002
8-other
Synthesis, structures, and strain energies of dispirophosphiranes. Comparisons with dispirocyclopropanes.
PMID 11950292·J Org Chem·2002
8-other
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
- 2500 N CHURCH ST
GREENSBORO, NC 27405 - Phone
- (276) 375-2240
Quick Facts
- NPI
- 1437455672
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 2
- Publications
- 13
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