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HOLLY STEWART, MD
MD
Psychiatry Physician
NPI: 1164453056IndividualAccepts Medicare
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
MD425191(PA)C55227(CA)
Education
UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE
Class of 2002
Research & Publications (20)
The impact of using emergency contraception on reproductive health outcomes: a retrospective review in an urban adolescent clinic.
PMID 14597021·J Pediatr Adolesc Gynecol·2003
4-observational
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
Clinicopathological phenotype of ALS with a novel G72C SOD1 gene mutation mimicking a myopathy.
PMID 16435343·Muscle Nerve·2006
5-case
Hydrodynamic consequences of flexural stiffness and buoyancy for seaweeds: a study using physical models.
PMID 16709919·J Exp Biol·2006
8-other
De novo deletion of chromosome 18q in a baby with harlequin ichthyosis.
PMID 11503161·Am J Med Genet·2001
5-case
One-at-a-time versus grouped presentation of mug book pictures: some surprising results.
PMID 11768071·J Appl Psychol·2001
8-other
Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family.
PMID 10729296·Br J Ophthalmol·2000
5-case
Sibs with developmental delay, hirsutism and nail hypoplasia: a new syndrome.
PMID 11045578·Clin Dysmorphol·2000
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
Galectin-1 stimulates monocyte chemotaxis via the p44/42 MAP kinase pathway and a pertussis toxin-sensitive pathway.
PMID 19561030·Glycobiology·2009
8-other
Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasia.
PMID 19250384·Clin Genet·2009
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
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
A large-scale mutation search reveals genetic heterogeneity in 3M syndrome.
PMID 19225462·Eur J Hum Genet·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
State-resolved UV photofragmentation spectrum of the metal dication complex [Zn(pyridine)(4)](2+).
PMID 18802513·Chem Commun (Camb)·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
- 412 E COMMONS
PITTSBURGH, PA 15212 - Phone
- (412) 323-4500
Quick Facts
- NPI
- 1164453056
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 24
- Publications
- 20
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