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STACY KANAGAWA, DO
DO
Pediatrics Physician
NPI: 1861438475Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
2002009355(MO)
Research & Publications (15)
Omphalocele in three generations with autosomal dominant transmission.
PMID 11897819·J Med Genet·2002
5-case
Gene organization in rice revealed by full-length cDNA mapping and gene expression analysis through microarray.
PMID 18043742·PLoS One·2007
8-other
Transforming growth factor beta 1 gene polymorphism in Japanese patients with systemic lupus erythematosus.
PMID 17579298·Kobe J Med Sci·2007
8-other
[A case of severe falciparum malaria successfully treated with intravenous artesunate and continuous hemodiafiltration].
PMID 17176859·Kansenshogaku Zasshi·2006
5-case
Effect of haemodialysis on retinal circulation in patients with end stage renal disease.
PMID 15258019·Br J Ophthalmol·2004
8-other
Exclusion of the TAP1 and TAP2 genes within the HLA class II region as candidate susceptibility genes to pemphigus in the Japanese population.
PMID 15519146·J Dermatol Sci·2004
8-other
Effect of mutated transporters associated with antigen-processing 2 on characteristic major histocompatibility complex binding peptides: analysis using electrospray ionization tandem mass spectrometry.
PMID 15116427·Rapid Commun Mass Spectrom·2004
8-other
Association of the TAP2*Bky2 allele with presence of SS-A/Ro and other autoantibodies in Japanese patients with systemic lupus erythematosus.
PMID 12729048·Lupus·2003
8-other
Thioredoxin as a biomarker for oxidative stress in patients with rheumatoid arthritis.
PMID 11841836·Mol Immunol·2002
8-other
New quadruplex structure of GGA triplet repeat DNA--an intramolecular quadruplex composed of a G:G:G:G tetrad and G(:A):G(:A):G(:A):G heptad, and its dimerization.
PMID 12836369·Nucleic Acids Res Suppl·2001
8-other
An intramolecular quadruplex of (GGA)(4) triplet repeat DNA with a G:G:G:G tetrad and a G(:A):G(:A):G(:A):G heptad, and its dimeric interaction.
PMID 11800555·J Mol Biol·2001
8-other
Creatine kinase gene mutation in a patient with muscle creatine kinase deficiency.
PMID 11673364·Clin Chem·2001
5-case
Polymorphisms of the mannose binding lectin gene in patients with Sjögren's syndrome.
PMID 11302870·Ann Rheum Dis·2001
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
- 940 W MOUNT VERNON ST
NIXA, MO 65714 - Phone
- (417) 724-5437
Quick Facts
- NPI
- 1861438475
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 15
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