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ERIC SWEENEY, MD
MD
Anesthesiology Physician
NPI: 1396206785IndividualAccepts Medicare
Specialties, Licenses & Credentials
Anesthesiology PhysicianPrimary
Anesthesiology
Code: 207L00000X
125.073641(IL)
CMS Specialties
PrimaryANESTHESIOLOGY
Education
UNIVERSITY OF IOWA, RJ & L CARVER COLLEGE OF MEDICINE
Class of 2019
Research & Publications (20)
Altered endochondral ossification in collagen X mouse models leads to impaired immune responses.
PMID 18629872·Dev Dyn·2008
7-preclinical
Nail patella syndrome: a review of the phenotype aided by developmental biology.
PMID 12624132·J Med Genet·2003
8-other
Sulfated polysaccharides increase plasma levels of SDF-1 in monkeys and mice: involvement in mobilization of stem/progenitor cells.
PMID 11756151·Blood·2002
7-preclinical
Nasomaxillary hypoplasia and severe orofacial clefting in a child of a mother with phenylketonuria.
PMID 11999984·J Inherit Metab Dis·2002
5-case
Increase in circulating SDF-1 after treatment with sulfated glycans. The role of SDF-1 in mobilization.
PMID 11458525·Ann N Y Acad Sci·2001
7-preclinical
Char syndrome: a new family and review of the literature emphasising the presence of symphalangism and the variable phenotype.
PMID 10955477·Clin Dysmorphol·2000
5-case
Mobilization of stem/progenitor cells by sulfated polysaccharides does not require selectin presence.
PMID 10841555·Proc Natl Acad Sci U S A·2000
7-preclinical
Ethics issues for HIV/AIDS researchers in international settings - perspectives from the Canadian experience.
PMID 18829360·Int J Infect Dis·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
Quantitative multiplexed quantum dot immunohistochemistry.
PMID 18621021·Biochem Biophys Res Commun·2008
8-other
A clinical and genetic study of the Say/Barber/Biesecker/Young-Simpson type of Ohdo syndrome.
PMID 18798845·Clin Genet·2008
8-other
Functional characterization of a novel insulin receptor mutation contributing to Rabson-Mendenhall syndrome.
PMID 17201797·Clin Endocrinol (Oxf)·2007
5-case
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
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
Molecular and clinical spectrum of type I plasminogen deficiency: A series of 50 patients.
PMID 16849641·Blood·2006
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 984455 NEBRASKA MEDICAL CTR
OMAHA, NE 68198 - Phone
- (402) 559-4081
Quick Facts
- NPI
- 1396206785
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 7
- Publications
- 20
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