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PAUL HART, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1750078689Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Utility of software analysis of esophageal manometry studies in patients with aperistalsis.
PMID 19021688·Dis Esophagus·2009
8-other
Qui non proficit, deficit: experimental models for 'integrative' research of affective disorders.
PMID 19428115·J Affect Disord·2010
6-review
Variation in aggregation propensities among ALS-associated variants of SOD1: correlation to human disease.
PMID 19483195·Hum Mol Genet·2009
8-other
Structural and biophysical properties of the pathogenic SOD1 variant H46R/H48Q.
PMID 19227972·Biochemistry·2009
7-preclinical
Genetic studies of craniofacial anomalies: clinical implications and applications.
PMID 19627523·Orthod Craniofac Res·2009
6-review
Activation of Cu,Zn-superoxide dismutase in the absence of oxygen and the copper chaperone CCS.
PMID 19542232·J Biol Chem·2009
7-preclinical
Understanding behavioral and physiological phenotypes of stress and anxiety in zebrafish.
PMID 19540270·Behav Brain Res·2009
7-preclinical
Exclusion of candidate genes in seven Turkish families with autosomal recessive amelogenesis imperfecta.
PMID 19530186·Am J Med Genet A·2009
5-case
Knemidokoptic mange in Hawai'i' Amakihi (Hemignathus virens) on the island of Hawai'i.
PMID 19395759·J Wildl Dis·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
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
Metal deficiency increases aberrant hydrophobicity of mutant superoxide dismutases that cause amyotrophic lateral sclerosis.
PMID 19651777·J Biol Chem·2009
8-other
Identifying catalytic residues in CPAF, a Chlamydia-secreted protease.
PMID 19388144·Arch Biochem Biophys·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
Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failure.
PMID 19664745·Am J Hum Genet·2009
8-other
Algorithms for digital image processing in diabetic retinopathy.
PMID 19616920·Comput Med Imaging Graph·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
- 601 ELMWOOD AVE
ROCHESTER, NY 14642 - Phone
- (585) 756-4800
Quick Facts
- NPI
- 1750078689
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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