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PHILIP CHUA, D.O.
D.O.
Family Medicine Physician
NPI: 1467433649IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
1833(WV)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
WEST VIRGINIA SCHOOL OF OSTEOPATHIC MEDICINE
Class of 1999
Research & Publications (20)
A longitudinal diffusion tensor imaging study in symptomatic Huntington's disease.
PMID 19237387·J Neurol Neurosurg Psychiatry·2010
8-other
Testing an electrostatic interaction hypothesis of hepatitis B virus capsid stability by using an in vitro capsid disassembly/reassembly system.
PMID 19656897·J Virol·2009
8-other
Recyclable organocatalysis: highly enantioselective Michael addition of 1,3-diaryl-1,3-propanedione to nitroolefins.
PMID 19322439·Chem Commun (Camb)·2009
8-other
Evaluating patient discomfort, anxiety, and fear before and after ranibizumab intravitreous injection for wet age-related macular degeneration.
PMID 19597121·Arch Ophthalmol·2009
8-other
Mapping retinal degeneration and loss-of-function in Rd-FTL mice.
PMID 19661224·Invest Ophthalmol Vis Sci·2009
7-preclinical
Rational design of organocatalyst: highly stereoselective Michael addition of cyclic ketones to nitroolefins.
PMID 19344184·Org Lett·2009
8-other
Modulation of alpha interferon anti-hepatitis C virus activity by ISG15.
PMID 19656964·J Gen Virol·2009
8-other
Quantitative identification of teratoma tissues formed by human embryonic stem cells with TeratomEye.
PMID 19169887·Biotechnol Lett·2009
8-other
Cell cycle arrest induced by hydrogen peroxide is associated with modulation of oxidative stress related genes in breast cancer cells.
PMID 19596828·Exp Biol Med (Maywood)·2009
8-other
Unusual domino michael/aldol condensation reactions employing oximes as N-selective nucleophiles: synthesis of N-hydroxypyrroles.
PMID 19130437·Angew Chem Int Ed Engl·2009
8-other
L-prolinol as a highly enantioselective catalyst for Michael addition of cyclohexanone to nitroolefins.
PMID 19359171·Bioorg Med Chem Lett·2009
8-other
A highly stereoselective organocatalytic tandem aminoxylation/aza-Michael reaction for the synthesis of tetrahydro-1,2-oxazines.
PMID 18788743·Org Lett·2008
8-other
Bioactive titanium implant surfaces with bacterial inhibition and osteoblast function enhancement properties.
PMID 18924089·Int J Artif Organs·2008
6-review
A highly diastereo- and enantioselective synthesis of multisubstituted cyclopentanes with four chiral carbons by the organocatalytic domino Michael-Henry reaction.
PMID 18630924·Org Lett·2008
8-other
Structural stability and bioapplicability assessment of hyaluronic acid-chitosan polyelectrolyte multilayers on titanium substrates.
PMID 18257066·J Biomed Mater Res A·2008
7-preclinical
Essential role of the N-terminal domain in the regulation of RIG-I ATPase activity.
PMID 18268020·J Biol Chem·2008
8-other
Organocatalytic asymmetric tandem Michael-Henry reactions: a highly stereoselective synthesis of multifunctionalized cyclohexanes with two quaternary stereocenters.
PMID 18489178·Org Lett·2008
8-other
The design and synthesis of potent and cell-active allosteric dual Akt 1 and 2 inhibitors devoid of hERG activity.
PMID 18550373·Bioorg Med Chem Lett·2008
8-other
Control of four stereocenters in an organocatalytic domino double Michael reaction: efficient synthesis of multisubstituted cyclopentanes.
PMID 18616339·Org Lett·2008
8-other
Centromere-associated protein E: a motor that puts the brakes on the mitotic checkpoint.
PMID 19047083·Clin Cancer Res·2008
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
- 812 GORMAN AVE
ELKINS, WV 26241 - Phone
- (304) 637-3188
Quick Facts
- NPI
- 1467433649
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 27
- Publications
- 20
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