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AMY ISAACS, PHARM.D.
PHARM.D.
Pharmacist
NPI: 1891161824Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
24316(NC)
Research & Publications (20)
Exercise Evaluation Randomised Trial (EXERT): a randomised trial comparing GP referral for leisure centre-based exercise, community-based walking and advice only.
PMID 17313906·Health Technol Assess·2007
4-observational
Acceleration of amyloid beta-peptide aggregation by physiological concentrations of calcium.
PMID 16870617·J Biol Chem·2006
7-preclinical
UK women doctors' use of hormone replacement therapy: 10-year follow up.
PMID 16096171·Climacteric·2005
8-other
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse.
PMID 12629167·J Neurosci·2003
7-preclinical
Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathy.
PMID 12359155·Mol Cell Neurosci·2002
7-preclinical
The apolipoprotein E gene and its age-specific effects on cognitive function.
PMID 19004527·Neurobiol Aging·2010
8-other
Heparin-induced thrombocytopenia: what clinicians need to know.
PMID 19190810·Thromb Haemost·2009
6-review
Design and synthesis of inhibitors of Hedgehog signaling based on the alkaloid cyclopamine.
PMID 19552464·Org Lett·2009
8-other
Presymptomatic generalized brain atrophy in frontotemporal dementia caused by CHMP2B mutation.
PMID 19202337·Dement Geriatr Cogn Disord·2009
5-case
De novo design and in vivo activity of conformationally restrained antimicrobial arylamide foldamers.
PMID 19359494·Proc Natl Acad Sci U S A·2009
7-preclinical
Cortical volumes and atrophy rates in FTD-3 CHMP2B mutation carriers and related non-carriers.
PMID 19150504·Neuroimage·2009
8-other
Genetic variation in the fibrinogen-alpha and fibrinogen-gamma genes in relation to arterial stiffness: the Rotterdam Study.
PMID 19412134·J Hypertens·2009
8-other
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.
PMID 19060911·Nat Genet·2009
8-other
Genome-wide linkage analysis of serum creatinine in three isolated European populations.
PMID 19387472·Kidney Int·2009
8-other
A study of the SORL1 gene in Alzheimer's disease and cognitive function.
PMID 19584446·J Alzheimers Dis·2009
4-observational
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis.
PMID 18952825·Hum Mol Genet·2009
8-other
Evolution of the aging brain transcriptome and synaptic regulation.
PMID 18830410·PLoS One·2008
7-preclinical
Patterns of hybrid loss of imprinting reveal tissue- and cluster-specific regulation.
PMID 18958286·PLoS One·2008
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 4408 NEW BERN AVE
RALEIGH, NC 27610 - Phone
- (919) 231-6419
Quick Facts
- NPI
- 1891161824
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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