Back to Search
HANNAH STEWART, MD
Student in an Organized Health Care Education/Training Program
NPI: 1073304549Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
57.259119(OH)
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
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
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
Assessment of a computer-based treatment for older amblyopes: the Glasgow Pilot Study.
PMID 17932508·Eye (Lond)·2009
8-other
Development of inducible EIAV-based lentiviral vector packaging and producer cell lines.
PMID 19262613·Gene Ther·2009
7-preclinical
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
A large-scale mutation search reveals genetic heterogeneity in 3M syndrome.
PMID 19225462·Eur J Hum 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
State-resolved UV photofragmentation spectrum of the metal dication complex [Zn(pyridine)(4)](2+).
PMID 18802513·Chem Commun (Camb)·2008
8-other
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.
PMID 18628315·J Med Genet·2008
8-other
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis.
PMID 18802454·PLoS Genet·2008
8-other
Congenital disseminated neurofibromatosis type 1: a clinical and molecular case report.
PMID 18438896·Am J Med Genet A·2008
5-case
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
No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome.
PMID 18541964·Clin Dysmorphol·2008
8-other
FISH mapping of de novo apparently balanced chromosome rearrangements identifies characteristics associated with phenotypic abnormality.
PMID 18374296·Am J Hum Genet·2008
4-observational
Lack of galectin-1 results in defects in myoblast fusion and muscle regeneration.
PMID 17366633·Dev Dyn·2007
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
- 1 WYOMING ST
DAYTON, OH 45409 - Phone
- (937) 208-3882
Quick Facts
- NPI
- 1073304549
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile