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VASVI SINGH, MD
MD
Cardiovascular Disease Physician
NPI: 1659652816IndividualAccepts Medicare
Specialties, Licenses & Credentials
Cardiovascular Disease PhysicianPrimary
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
04-44236(KS)
Education
OTHER
Class of 2010
Research & Publications (20)
Diels-Alder cycloaddition and ring-closing metathesis: a versatile, stereoselective, and general route to embellished bridged bicyclic systems, carbocyclic framework of secoatisanes, and homologues.
PMID 19610638·J Org Chem·2009
8-other
Splash in elective primary knee and hip replacement: are we adequately protected?
PMID 19651837·J Bone Joint Surg Br·2009
8-other
Insertional inactivation of branched-chain alpha-keto acid dehydrogenase in Staphylococcus aureus leads to decreased branched-chain membrane fatty acid content and increased susceptibility to certain stresses.
PMID 18689519·Appl Environ Microbiol·2008
7-preclinical
Molecular complexity from aromatics: a novel, stereoselective route to tricyclo[5.2.2.0(1,5)]undecenones, tricyclo[6.2.2.0(1,6)]dodecenones, and [n.3.3]propellanes.
PMID 18047375·J Org Chem·2007
8-other
Role for dnaK locus in tolerance of multiple stresses in Staphylococcus aureus.
PMID 17768259·Microbiology (Reading)·2007
7-preclinical
Cycloaddition of cyclohexa-2,4-dienones, ring-closing metathesis, and photochemical reactions: a common stereoselective approach to duprezianane, polyquinane and sterpurane frameworks.
PMID 17311459·J Org Chem·2007
8-other
Cycloaddition between electron-deficient pi-systems, photochemical and radical-induced reactions: a novel, general, and stereoselective route to polyfunctionalized bridged bicyclo[2.2.2]octanes, bicyclo[3.3.0]octanes, bicyclo[4.2.0]octanes, and tricyclo[4.3.1.0(3,7)]decanes.
PMID 16599596·J Org Chem·2006
8-other
Molecular complexity from aromatics: synthesis and photoreaction of endo-tricyclo[5.2.2.0(2,6)]undecane--a stereoselective route to tricyclic framework of protoilludanes.
PMID 15990294·Bioorg Med Chem Lett·2005
8-other
A novel and efficient synthesis of bicyclo[2.2.2]octenones and sigmatropic shifts in ground and excited states: stereoselective route to cis-decalins and diquinane frameworks.
PMID 15675857·J Org Chem·2005
8-other
Efficient stereoselective synthesis of novel steroid-polyquinane hybrids.
PMID 12816408·Org Lett·2003
8-other
Cycloaddition of cyclohexa-2,4-dienones with electron deficient 2 pi partners: a novel and stereoselective route to functionalized bicyclo[2.2.2]octenones.
PMID 12357773·Chem Commun (Camb)·2002
8-other
Role of cytokines in experimental and clinical uveitis.
PMID 15884511·Indian J Ophthalmol·2001
6-review
Structural diversity through intramolecular cycloaddition and modulation of chemical reactivity in excited state. Synthesis and photoreactions of 3-oxa-tricyclo[5.2.2.0(1,5)]undecenones: novel stereoselective route to oxa-triquinanes and oxa-sterpuranes.
PMID 11086719·Bioorg Med Chem Lett·2000
8-other
Trace element concentration in groundwater of Pesarlanka Island, Krishna Delta, India.
PMID 19267209·Environ Monit Assess·2010
8-other
Effect of resistant starch on hydrolysis and fermentation of corn starch for ethanol.
PMID 19415528·Appl Biochem Biotechnol·2010
8-other
Tuberculous cervical lymphadenitis in a patient with laryngeal carcinoma.
PMID 19646297·J Laryngol Otol·2010
5-case
Efficacy of electrical resistivity and induced polarization methods for revealing fluoride contaminated groundwater in granite terrain.
PMID 19626445·Environ Monit Assess·2010
8-other
Gluon-spin contribution to the proton spin from the double-helicity asymmetry in inclusive pi0 production in polarized p+p collisions at [sqrt]s=200 GeV.
PMID 19659137·Phys Rev Lett·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
- 5100 W 110TH ST STE 200
OVERLAND PARK, KS 66211 - Phone
- (913) 253-3000
Quick Facts
- NPI
- 1659652816
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 16
- Publications
- 20
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