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HEATHER STEWART, PHARMD
PHARMD
Pharmacist
NPI: 1659780450Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
PR27905(ME)
Research & Publications (20)
Substrate-induced phenotypical change of monocytes/macrophages into myofibroblast-like cells: a new insight into the mechanism of in-stent restenosis.
PMID 18546184·J Biomed Mater Res A·2009
8-other
Development of inducible EIAV-based lentiviral vector packaging and producer cell lines.
PMID 19262613·Gene Ther·2009
7-preclinical
Congenital disseminated neurofibromatosis type 1: a clinical and molecular case report.
PMID 18438896·Am J Med Genet A·2008
5-case
In vivo models for the study of transplantation tolerance.
PMID 17876103·Methods Mol Biol·2007
7-preclinical
Hydrodynamic consequences of flexural stiffness and buoyancy for seaweeds: a study using physical models.
PMID 16709919·J Exp Biol·2006
8-other
Clinicopathological phenotype of ALS with a novel G72C SOD1 gene mutation mimicking a myopathy.
PMID 16435343·Muscle Nerve·2006
5-case
Corticomotoneuronal dysfunction in ALS patients with different SOD1 mutations.
PMID 16793335·Clin Neurophysiol·2006
4-observational
Determinants of coital frequency among married women in Central African Republic: the role of female genital cutting.
PMID 12395867·J Biosoc Sci·2002
8-other
One-at-a-time versus grouped presentation of mug book pictures: some surprising results.
PMID 11768071·J Appl Psychol·2001
8-other
De novo deletion of chromosome 18q in a baby with harlequin ichthyosis.
PMID 11503161·Am J Med Genet·2001
5-case
Developmental regulation and overexpression of the transcription factor AP-2, a potential regulator of the timing of Schwann cell generation.
PMID 11553286·Eur J Neurosci·2001
7-preclinical
Sibs with developmental delay, hirsutism and nail hypoplasia: a new syndrome.
PMID 11045578·Clin Dysmorphol·2000
5-case
Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family.
PMID 10729296·Br J Ophthalmol·2000
5-case
A large-scale mutation search reveals genetic heterogeneity in 3M syndrome.
PMID 19225462·Eur J Hum Genet·2009
8-other
Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasia.
PMID 19250384·Clin Genet·2009
5-case
Air transport of patients with severe lung injury: development and utilization of the Acute Lung Rescue Team.
PMID 19359961·J Trauma·2009
8-other
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.
PMID 19372089·J Med Genet·2009
8-other
Galectin-1 stimulates monocyte chemotaxis via the p44/42 MAP kinase pathway and a pertussis toxin-sensitive pathway.
PMID 19561030·Glycobiology·2009
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
- 600 ROUNDWOOD DR
SCARBOROUGH, ME 04074 - Phone
- (207) 710-7047
Quick Facts
- NPI
- 1659780450
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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