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MATTHEW MELIN, MD
MD
Vascular Surgery Physician
NPI: 1730166992IndividualAccepts Medicare
Specialties, Licenses & Credentials
Phlebology Physician
Phlebology
Code: 202K00000X
036143875(IL)
Surgery Physician
Surgery
Code: 208600000X
35464(MN)
Vascular Surgery PhysicianPrimary
Surgery — Vascular Surgery
Code: 2086S0129X
036143875(IL)35464(MN)
Education
UNIVERSITY OF MINNESOTA MEDICAL SCHOOL
Class of 1997
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
Confocal laser scanning microscopy using dialkylcarbocyanine dyes for cell tracing in hard and soft biomaterials.
PMID 16924608·J Biomed Mater Res B Appl Biomater·2007
7-preclinical
A founder mutation for ichthyosis prematurity syndrome restricted to 76 kb by haplotype association.
PMID 16946994·J Hum Genet·2006
8-other
Constitutional downregulation of SEMA5A expression in autism.
PMID 17028446·Neuropsychobiology·2006
4-observational
Adult-onset autosomal dominant leukodystrophy with autonomic symptoms restricted to 1.5 Mbp on chromosome 5q23.
PMID 16823806·Am J Med Genet B Neuropsychiatr Genet·2006
8-other
Unsuccessful peripherally inserted central catheter placement.
PMID 16687762·J Vasc Interv Radiol·2006
5-case
Analysis of feeding and drinking patterns of dairy cows in two cow traffic situations in automatic milking systems.
PMID 15591369·J Dairy Sci·2005
7-preclinical
Feeding patterns and performance of cows in controlled cow traffic in automatic milking systems.
PMID 16230697·J Dairy Sci·2005
4-observational
[Cellular culture of osteoblasts and fibroblasts on porous calcium-phosphate bone substitutes].
PMID 12610435·Rev Chir Orthop Reparatrice Appar Mot·2003
8-other
Effect of micro- and macroporosity of bone substitutes on their mechanical properties and cellular response.
PMID 15348502·J Mater Sci Mater Med·2003
8-other
TGF-beta1 induces accumulation of dendritic cells in the odontoblast layer.
PMID 12885853·J Dent Res·2003
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 6405 FRANCE AVE S STE W440
EDINA, MN 55435 - Phone
- (952) 927-7004
Quick Facts
- NPI
- 1730166992
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 4
- Locations
- 2
- Years in Practice
- 29
- Publications
- 20
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