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IVAN HANSON, MD
MD
Internal Medicine Physician
NPI: 1649470055IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
4301086414(MI)
Education
WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE
Class of 2005
Research & Publications (20)
Evidence of nerve sheath differentiation and high grade morphology in sclerosing epithelioid fibrosarcoma.
PMID 11533083·J Clin Pathol·2001
5-case
Lichen planus associated with omalizumab administration in an adult with allergic asthma.
PMID 19445051·Ann Allergy Asthma Immunol·2009
5-case
Role of IL-7 in the regulation of T-cell homeostasis in partial DiGeorge syndrome.
PMID 19230961·J Allergy Clin Immunol·2009
8-other
Long-term outcomes of nonconditioned patients with severe combined immunodeficiency transplanted with HLA-identical or haploidentical bone marrow depleted of T cells with anti-CD6 mAb.
PMID 19084111·J Allergy Clin Immunol·2008
4-observational
Methicillin-susceptible Staphylococcus aureus brain abscess in common variable immunodeficiency after an 8-month gap in return to the immunologist.
PMID 18760457·J Allergy Clin Immunol·2008
8-other
Sequences encoded in the class II region of the MHC related to the 'ABC' superfamily of transporters. 1990.
PMID 18292489·J Immunol·2008
7-preclinical
Inherited PAX6, NF1 and OTX2 mutations in a child with microphthalmia and aniridia.
PMID 17406642·Eur J Hum Genet·2007
5-case
A screen for proteins that interact with PAX6: C-terminal mutations disrupt interaction with HOMER3, DNCL1 and TRIM11.
PMID 16098226·BMC Genet·2005
8-other
Expression analysis of SIX3 and SIX6 in human tissues reveals differences in expression and a novel correlation between the expression of SIX3 and the genes encoding isocitrate dehyhrogenase and cadherin 18.
PMID 15953543·Genomics·2005
4-observational
Heterozygous mutations of OTX2 cause severe ocular malformations.
PMID 15846561·Am J Hum Genet·2005
4-observational
Mechanistic actions of the risks and adverse events associated with vaccine administration.
PMID 15536401·J Allergy Clin Immunol·2004
6-review
Absence of SIX6 mutations in microphthalmia, anophthalmia, and coloboma.
PMID 15505031·Invest Ophthalmol Vis Sci·2004
8-other
Polymicrogyria and absence of pineal gland due to PAX6 mutation.
PMID 12731001·Ann Neurol·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
- Address
- 50 E CANFIELD ST
DETROIT, MI 48201 - Phone
- (313) 745-4525
Quick Facts
- NPI
- 1649470055
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 21
- Publications
- 20
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