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PHILIP HART, M.D.
M.D.
Gastroenterology Physician
NPI: 1295939361IndividualAccepts Medicare
Specialties, Licenses & Credentials
Gastroenterology PhysicianPrimary
Internal Medicine — Gastroenterology
Code: 207RG0100X
35.124022(OH)
Education
UNIVERSITY OF MISSOURI, COLUMBIA SCHOOL OF MEDICINE
Class of 2007
Research & Publications (20)
Competencies most valued by employers--Implications for master's-prepared occupational health nurses.
PMID 16862880·AAOHN J·2006
8-other
Qui non proficit, deficit: experimental models for 'integrative' research of affective disorders.
PMID 19428115·J Affect Disord·2010
6-review
Genetic studies of craniofacial anomalies: clinical implications and applications.
PMID 19627523·Orthod Craniofac Res·2009
6-review
Structural and biophysical properties of the pathogenic SOD1 variant H46R/H48Q.
PMID 19227972·Biochemistry·2009
7-preclinical
Amino acid changes in elongation factor Tu of Mycoplasma pneumoniae and Mycoplasma genitalium influence fibronectin binding.
PMID 19546194·Infect Immun·2009
8-other
Understanding behavioral and physiological phenotypes of stress and anxiety in zebrafish.
PMID 19540270·Behav Brain Res·2009
7-preclinical
Identifying catalytic residues in CPAF, a Chlamydia-secreted protease.
PMID 19388144·Arch Biochem Biophys·2009
8-other
Algorithms for digital image processing in diabetic retinopathy.
PMID 19616920·Comput Med Imaging Graph·2009
4-observational
Variation in aggregation propensities among ALS-associated variants of SOD1: correlation to human disease.
PMID 19483195·Hum Mol Genet·2009
8-other
Activation of Cu,Zn-superoxide dismutase in the absence of oxygen and the copper chaperone CCS.
PMID 19542232·J Biol Chem·2009
7-preclinical
Role of mutant SOD1 disulfide oxidation and aggregation in the pathogenesis of familial ALS.
PMID 19416874·Proc Natl Acad Sci U S A·2009
7-preclinical
Phenotypic variation in FAM83H-associated amelogenesis imperfecta.
PMID 19407157·J Dent Res·2009
8-other
Knemidokoptic mange in Hawai'i' Amakihi (Hemignathus virens) on the island of Hawai'i.
PMID 19395759·J Wildl Dis·2009
7-preclinical
Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failure.
PMID 19664745·Am J Hum Genet·2009
8-other
Immature copper-zinc superoxide dismutase and familial amyotrophic lateral sclerosis.
PMID 19596823·Exp Biol Med (Maywood)·2009
6-review
Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta.
PMID 19220331·Clin Genet·2009
8-other
Exclusion of candidate genes in seven Turkish families with autosomal recessive amelogenesis imperfecta.
PMID 19530186·Am J Med Genet A·2009
5-case
The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P.
PMID 19092777·Eur J Hum Genet·2009
8-other
Metal deficiency increases aberrant hydrophobicity of mutant superoxide dismutases that cause amyotrophic lateral sclerosis.
PMID 19651777·J Biol Chem·2009
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
- 410 W 10TH AVE
COLUMBUS, OH 43210 - Phone
- (614) 293-6255
Quick Facts
- NPI
- 1295939361
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 19
- Publications
- 20
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