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HANNAH STEWART, PHARMD
PHARMD
Pharmacist
NPI: 1689191900Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
26000(NC)
Research & Publications (20)
Development of inducible EIAV-based lentiviral vector packaging and producer cell lines.
PMID 19262613·Gene Ther·2009
7-preclinical
Corticomotoneuronal dysfunction in ALS patients with different SOD1 mutations.
PMID 16793335·Clin Neurophysiol·2006
4-observational
Clinicopathological phenotype of ALS with a novel G72C SOD1 gene mutation mimicking a myopathy.
PMID 16435343·Muscle Nerve·2006
5-case
Electromyography of respiratory muscles in amyotrophic lateral sclerosis.
PMID 11676994·J Neurol Sci·2001
8-other
Scottish adjuvant tamoxifen trial: a randomized study updated to 15 years.
PMID 11259471·J Natl Cancer Inst·2001
3-trial
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
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
A large-scale mutation search reveals genetic heterogeneity in 3M syndrome.
PMID 19225462·Eur J Hum Genet·2009
8-other
Air transport of patients with severe lung injury: development and utilization of the Acute Lung Rescue Team.
PMID 19359961·J Trauma·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
Assessment of a computer-based treatment for older amblyopes: the Glasgow Pilot Study.
PMID 17932508·Eye (Lond)·2009
8-other
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
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.
PMID 18550696·J Med Genet·2009
8-other
Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasia.
PMID 19250384·Clin Genet·2009
5-case
FISH mapping of de novo apparently balanced chromosome rearrangements identifies characteristics associated with phenotypic abnormality.
PMID 18374296·Am J Hum Genet·2008
4-observational
SOD1 gene mutations in ALS patients from British Columbia, Canada: clinical features, neurophysiology and ethical issues in management.
PMID 18428003·Amyotroph Lateral Scler·2008
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
- 110 PARK AVE
BANNER ELK, NC 28604 - Phone
- (828) 898-4271
Quick Facts
- NPI
- 1689191900
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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