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MATTHEW KWON, MD
MD
Emergency Medicine Physician
NPI: 1780115790Individual
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
ME141499(FL)83893(SC)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
No effects of mobile phone electromagnetic field on auditory brainstem response.
PMID 19610044·Bioelectromagnetics·2010
8-other
Quantitative and rapid analysis of transglutaminase activity using protein arrays in mammalian cells.
PMID 19326081·Mol Cells·2009
7-preclinical
A novel splice site mutation in the EYA1 gene in a Korean family with branchio-oto (BO) syndrome.
PMID 18763178·Acta Otolaryngol·2009
5-case
One-pot synthesis of imines and secondary amines by Pd-catalyzed coupling of benzyl alcohols and primary amines.
PMID 19265414·J Org Chem·2009
8-other
Preattentive auditory information processing under exposure to the 902 MHz GSM mobile phone electromagnetic field: a mismatch negativity (MMN) study.
PMID 19140136·Bioelectromagnetics·2009
8-other
Use of ventricular assist device as a bridge to cardiac transplantation: impact of age and other determinants on outcomes.
PMID 19568390·Tex Heart Inst J·2009
4-observational
Biotransformation products and mineralization potential for hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) in abiotic versus biological degradation pathways with anthraquinone-2,6-disulfonate (AQDS) and Geobacter metallireducens.
PMID 18239998·Biodegradation·2008
8-other
Generation of transgenic chickens that produce bioactive human granulocyte-colony stimulating factor.
PMID 18196568·Mol Reprod Dev·2008
7-preclinical
Perception of the electromagnetic field emitted by a mobile phone.
PMID 18027840·Bioelectromagnetics·2008
8-other
Severe factor XI deficiency in a Korean woman with a novel missense mutation (Val498Met) and duplication G mutation in exon 13 of the F11 gene.
PMID 18832909·Blood Coagul Fibrinolysis·2008
5-case
Mechanisms to suppress multipolar divisions in cancer cells with extra centrosomes.
PMID 18662975·Genes Dev·2008
7-preclinical
Identification of mutations in the F9 gene including exon deletion by multiplex ligation-dependent probe amplification in 33 unrelated Korean patients with haemophilia B.
PMID 18624698·Haemophilia·2008
8-other
Antitumor effect of a transducible fusogenic peptide releasing multiple proapoptotic peptides by caspase-3.
PMID 18566222·Mol Cancer Ther·2008
7-preclinical
[Evaluation of GLUCOCARD X-METER glucose monitoring system].
PMID 18309250·Korean J Lab Med·2008
8-other
Role of PKCdelta in IFN-gamma-inducible CIITA gene expression.
PMID 17346795·Mol Immunol·2007
7-preclinical
Magnetically separable Pd catalyst for highly selective epoxide hydrogenolysis under mild conditions.
PMID 17661475·Org Lett·2007
8-other
Association between apolipoprotein E genetic polymorphism and the development of diabetic nephropathy in type 2 diabetic patients.
PMID 17624465·Diabetes Res Clin Pract·2007
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
- 316 CALHOUN ST
CHARLESTON, SC 29401 - Phone
- (843) 724-2010
Quick Facts
- NPI
- 1780115790
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 1
- Publications
- 20
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