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THOMAS HART, MD
MD
Surgery Physician
NPI: 1326084773Individual
Specialties, Licenses & Credentials
Surgery PhysicianPrimary
Surgery
Code: 208600000X
27769(KY)
Research & Publications (20)
Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failure.
PMID 19664745·Am J Hum Genet·2009
8-other
Genetic studies of craniofacial anomalies: clinical implications and applications.
PMID 19627523·Orthod Craniofac Res·2009
6-review
Treatment definition in complex rehabilitation interventions.
PMID 19544183·Neuropsychol Rehabil·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
Expected values for pedometer-determined physical activity in youth.
PMID 19650381·Res Q Exerc Sport·2009
6-review
Fatty acid amide hydrolase inhibitors. Surprising selectivity of chiral azetidine ureas.
PMID 19515560·Bioorg Med Chem Lett·2009
7-preclinical
Caregivers' well-being after traumatic brain injury: a multicenter prospective investigation.
PMID 19480869·Arch Phys Med Rehabil·2009
4-observational
Phenotypic variation in FAM83H-associated amelogenesis imperfecta.
PMID 19407157·J Dent Res·2009
8-other
Unexplained excess of electronlike events from a 1-GeV neutrino beam.
PMID 19392103·Phys Rev Lett·2009
8-other
Effects of therapeutic massage on the quality of life among patients with breast cancer during treatment.
PMID 19388859·J Altern Complement Med·2009
3-trial
Folding kinetics of the human prion protein probed by temperature jump.
PMID 19321423·Proc Natl Acad Sci U S A·2009
8-other
Measurement of numicro and nue events in an off-axis horn-focused neutrino beam.
PMID 19519094·Phys Rev Lett·2009
8-other
Hutchinson-Gilford progeria syndrome: oral and craniofacial phenotypes.
PMID 19236595·Oral Dis·2009
8-other
Candidate selection and preclinical evaluation of N-tert-butyl isoquine (GSK369796), an affordable and effective 4-aminoquinoline antimalarial for the 21st century.
PMID 19222165·J Med Chem·2009
7-preclinical
Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta.
PMID 19220331·Clin Genet·2009
8-other
Race/ethnicity differences in satisfaction with life among persons with traumatic brain injury.
PMID 19208953·NeuroRehabilitation·2009
4-observational
Enamel defects and salivary methylmalonate in methylmalonic acidemia.
PMID 19143946·Oral Dis·2009
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
- 1031 NEW MOODY LN, SUITE 200
LA GRANGE, KY 40031 - Phone
- (502) 225-9877
Quick Facts
- NPI
- 1326084773
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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