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MICHAEL MELIN, M.D.
M.D.
Anesthesiology Physician
NPI: 1215270780IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Code: 390200000X
CMS Specialties
PrimaryANESTHESIOLOGY
Education
OTHER
Class of 2013
Research & Publications (20)
Streptococcus pneumoniae capsular serotype 19F is more resistant to C3 deposition and less sensitive to opsonophagocytosis than serotype 6B.
PMID 19047408·Infect Immun·2009
8-other
Development of antibodies to PspA families 1 and 2 in children after exposure to Streptococcus pneumoniae.
PMID 18753341·Clin Vaccine Immunol·2008
8-other
Distribution of pneumococcal surface protein A families 1 and 2 among Streptococcus pneumoniae isolates from children in finland who had acute otitis media or were nasopharyngeal carriers.
PMID 18753340·Clin Vaccine Immunol·2008
8-other
Central nervous system involvement in severe congenital neutropenia: neurological and neuropsychological abnormalities associated with specific HAX1 mutations.
PMID 18513342·J Intern Med·2008
5-case
Interleukin-6 (IL-6) and/or soluble IL-6 receptor down-regulation of human type II collagen gene expression in articular chondrocytes requires a decrease of Sp1.Sp3 ratio and of the binding activity of both factors to the COL2A1 promoter.
PMID 18065760·J Biol Chem·2008
7-preclinical
Changes in the ST-interval segment of the fetal electrocardiogram in relation to acid-base status at birth.
PMID 19035941·BJOG·2008
8-other
Antibodies to pneumococcal surface protein A families 1 and 2 in serum and saliva of children and the risk of pneumococcal acute otitis media.
PMID 18008233·J Infect Dis·2007
8-other
Kostmann syndrome or infantile genetic agranulocytosis, part two: Understanding the underlying genetic defects in severe congenital neutropenia.
PMID 17537008·Acta Paediatr·2007
6-review
Assignment of the gene locus for severe congenital neutropenia to chromosome 1q22 in the original Kostmann family from Northern Sweden.
PMID 17188649·Biochem Biophys Res Commun·2007
8-other
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).
PMID 17187068·Nat Genet·2007
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
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Contact & Hours
Via practice · 2 locations total
- Address
- 400 S 43RD ST
RENTON, WA 98055 - Phone
- (800) 540-1814
Quick Facts
- NPI
- 1215270780
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 2
- Years in Practice
- 13
- Publications
- 20
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