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BRENDAN SMITH, M.D.
M.D.
Orthopaedic Surgery Physician
NPI: 1649895178IndividualAccepts Medicare
Specialties, Licenses & Credentials
Orthopaedic Surgery PhysicianPrimary
Orthopaedic Surgery
Code: 207X00000X
MT221401(PA)MD480285(PA)
CMS Specialties
PrimaryORTHOPEDIC SURGERY
Education
RUTGERS NEW JERSEY MEDICAL SCHOOL
Class of 2020
Research & Publications (20)
Predicting the anticipated emotional and behavioral responses to an avian flu outbreak.
PMID 19121548·Am J Infect Control·2009
7-preclinical
A continuous microplate assay for sirtuins and nicotinamide-producing enzymes.
PMID 19615966·Anal Biochem·2009
7-preclinical
Influence of surface oxides on the colloidal stability of multi-walled carbon nanotubes: a structure-property relationship.
PMID 19583226·Langmuir·2009
8-other
Listeria monocytogenes: maternal-foetal infections in Denmark 1994-2005.
PMID 18855227·Scand J Infect Dis·2009
8-other
Low body mass index: a risk factor for superior mesenteric artery syndrome in adolescents undergoing spinal fusion for scoliosis.
PMID 19342937·J Spinal Disord Tech·2009
5-case
Five-nanometer diamond with luminescent nitrogen-vacancy defect centers.
PMID 19334016·Small·2009
8-other
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6.
PMID 19251628·Science·2009
7-preclinical
Colloidal properties of aqueous suspensions of acid-treated, multi-walled carbon nanotubes.
PMID 19245021·Environ Sci Technol·2009
8-other
Extreme aggressiveness and lethality of gastric adenocarcinoma in the very young.
PMID 19528381·Arch Surg·2009
4-observational
Retinal pigment epithelial tears in ranibizumab-treated eyes.
PMID 19174716·Retina·2009
4-observational
Neural substrates of reward magnitude, probability, and risk during a wheel of fortune decision-making task.
PMID 18804540·Neuroimage·2009
8-other
The role of resilience and purpose in life in habituation to heat and cold pain.
PMID 19345153·J Pain·2009
8-other
Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype.
PMID 19459885·Clin Genet·2009
5-case
Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindreds.
PMID 19036076·Br J Haematol·2009
8-other
Chemical mechanisms of histone lysine and arginine modifications.
PMID 18603028·Biochim Biophys Acta·2009
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 801 OSTRUM ST
BETHLEHEM, PA 18015 - Phone
- (866) 785-8537
Quick Facts
- NPI
- 1649895178
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 6
- Publications
- 20
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