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KEVIN ERICSON, MD
MD
Family Medicine Physician
NPI: 1265458749IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
01046492(IN)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE
Class of 1986
Research & Publications (20)
N-methylpyridoxamine: novel canine vitamin B6 urine metabolite.
PMID 18295484·Bioorg Med Chem Lett·2008
7-preclinical
Use of chlorite to improve HPLC detection of pyridoxal 5'-phosphate.
PMID 16054880·J Chromatogr B Analyt Technol Biomed Life Sci·2005
4-observational
Immunohistochemical Loss of the DNA Mismatch Repair Proteins MSH2 and MSH6 in Malignant Fibrous Histiocytomas.
PMID 18521406·Sarcoma·2004
8-other
Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis.
PMID 12483306·Hum Genet·2003
8-other
Eyewitness identification accuracy: a comparison of adults with and those without intellectual disabilities.
PMID 12737610·Ment Retard·2003
4-observational
Relationship of Chlamydia pneumoniae infection to severity of human coronary atherosclerosis.
PMID 10840006·Circulation·2000
8-other
Nutritional status assessment before, during, and after long-duration head-down bed rest.
PMID 19476165·Aviat Space Environ Med·2009
8-other
Effects of 21 days of bed rest, with or without artificial gravity, on nutritional status of humans.
PMID 19074571·J Appl Physiol (1985)·2009
8-other
De novo induction of genetically engineered brain tumors in mice using plasmid DNA.
PMID 19147555·Cancer Res·2009
7-preclinical
The relationship between idiopathic intracranial hypertension and obesity.
PMID 19222591·Headache·2009
8-other
Stability of analytes related to clinical chemistry and bone metabolism in blood specimens after delayed processing.
PMID 19250930·Clin Biochem·2009
5-case
Persistence of CD133+ cells in human and mouse glioma cell lines: detailed characterization of GL261 glioma cells with cancer stem cell-like properties.
PMID 18271701·Stem Cells Dev·2008
7-preclinical
Autosomal recessive hypophosphatasia manifesting in utero with long bone deformity but showing spontaneous postnatal improvement.
PMID 18559907·J Clin Endocrinol Metab·2008
5-case
Capsulotomy for obsessive-compulsive disorder: long-term follow-up of 25 patients.
PMID 18678796·Arch Gen Psychiatry·2008
8-other
Expression of MHC I and NK ligands on human CD133+ glioma cells: possible targets of immunotherapy.
PMID 17077937·J Neurooncol·2007
4-observational
Lymphocytic hypophysitis: report of two biopsy-proven cases and one suspected case with pituitary autoantibodies.
PMID 17392607·J Endocrinol Invest·2007
5-case
Pyridoxine-responsive seizures as the first symptom of infantile hypophosphatasia caused by two novel missense mutations (c.677T>C, p.M226T; c.1112C>T, p.T371I) of the tissue-nonspecific alkaline phosphatase gene.
PMID 17395561·Bone·2007
5-case
Transposon-based interferon gamma gene transfer overcomes limitations of episomal plasmid for immunogene therapy of glioblastoma.
PMID 17415381·Cancer Gene Ther·2007
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 611 E DOUGLAS RD
MISHAWAKA, IN 46545 - Phone
- (574) 335-6500
Quick Facts
- NPI
- 1265458749
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 40
- Publications
- 20
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