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EMILY SWEENEY, M.D.
M.D.
Pediatric Orthopaedic Surgery Physician
NPI: 1639497142Individual
Specialties, Licenses & Credentials
Pediatric Sports Medicine Physician
Pediatrics — Sports Medicine
Code: 2080S0010X
DR.0056029(CO)
Pediatric Orthopaedic Surgery PhysicianPrimary
Orthopaedic Surgery — Pediatric Orthopaedic Surgery
Code: 207XP3100X
DR.0056029(CO)
Research & Publications (20)
Quantitative multiplexed quantum dot immunohistochemistry.
PMID 18621021·Biochem Biophys Res Commun·2008
8-other
Ethics issues for HIV/AIDS researchers in international settings - perspectives from the Canadian experience.
PMID 18829360·Int J Infect Dis·2008
8-other
Altered endochondral ossification in collagen X mouse models leads to impaired immune responses.
PMID 18629872·Dev Dyn·2008
7-preclinical
A clinical and genetic study of the Say/Barber/Biesecker/Young-Simpson type of Ohdo syndrome.
PMID 18798845·Clin Genet·2008
8-other
Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype.
PMID 18452192·Am J Med Genet A·2008
8-other
A molecular and clinical study of Larsen syndrome caused by mutations in FLNB.
PMID 16801345·J Med Genet·2007
8-other
RAB23 mutations in Carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesity.
PMID 17503333·Am J Hum Genet·2007
8-other
Functional characterization of a novel insulin receptor mutation contributing to Rabson-Mendenhall syndrome.
PMID 17201797·Clin Endocrinol (Oxf)·2007
5-case
Multiple renal cysts, ear anomalies, disordered hair growth and unusual facies: a new entity?
PMID 16531743·Clin Dysmorphol·2006
5-case
An item gains and losses analysis of false memories suggests critical items receive more item-specific processing than list items.
PMID 16569146·J Exp Psychol Learn Mem Cogn·2006
4-observational
The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males.
PMID 16685650·Am J Hum Genet·2006
8-other
Mutations in two regions of FLNB result in atelosteogenesis I and III.
PMID 16752402·Hum Mutat·2006
8-other
Pfeiffer-type cardiocranial syndrome: a patient with features of this condition and with an unbalanced subtelomeric rearrangement involving chromosomes 1p and 17q.
PMID 16531733·Clin Dysmorphol·2006
5-case
The effect of telephone appointment-reminder calls on outpatient absenteeism in a pulmonary function laboratory.
PMID 16381615·Respir Care·2006
8-other
Molecular and clinical spectrum of type I plasminogen deficiency: A series of 50 patients.
PMID 16849641·Blood·2006
4-observational
Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patients.
PMID 16183801·J Med Genet·2006
8-other
Pontomedullary disconnection: fetal and neonatal considerations.
PMID 15812634·Pediatr Radiol·2005
5-case
Nail patella syndrome revisited: 50 years after linkage.
PMID 15996164·Ann Hum Genet·2005
7-preclinical
Psychosocial risk factors for postherpetic neuralgia: a prospective study of patients with herpes zoster.
PMID 16326366·J Pain·2005
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
- 13123 E 16TH AVE
AURORA, CO 80045 - Phone
- (720) 777-1234
Quick Facts
- NPI
- 1639497142
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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