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STEVEN KOHL, DO
DO
Family Medicine Physician
NPI: 1245229541IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
5101013046(MI)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
MICHIGAN STATE UNIVERSITY COLLEGE OF OSTEOPATHIC MEDICINE
Class of 1996
Research & Publications (20)
Chondroid metaplasia mimicking recurrent squamous cell carcinoma of the head and neck.
PMID 19172559·Ear Nose Throat J·2009
5-case
Consecutive thermal H2 and light-induced O2 evolution from water promoted by a metal complex.
PMID 19342584·Science·2009
8-other
Clinical significance of benign glands at surgical margins in robotic radical prostatectomy specimens.
PMID 17572197·Urology·2007
3-trial
Solvent dependent reactivity: solvent activation vs. solvent coordination in alkylphosphane iron complexes.
PMID 17225895·Dalton Trans·2006
8-other
Ligand cleavage put into reverse: P--C bond breaking and remaking in an alkylphosphane iron complex.
PMID 16528780·Chemistry·2006
8-other
Renal hilar mass in an 85-year-old woman. Solitary fibrous tumor.
PMID 16390227·Arch Pathol Lab Med·2006
5-case
FDG uptake in giant cell tumor of the tendon sheath in a patient restaged for gastrointestinal stroma tumor (GIST).
PMID 19352292·Clin Nucl Med·2009
5-case
An aluminium mold for intraoperative production of antibiotic-loaded PMMA knee prostheses.
PMID 19424917·Acta Orthop·2009
8-other
Mutations in the GUCA1A gene involved in hereditary cone dystrophies impair calcium-mediated regulation of guanylate cyclase.
PMID 19459154·Hum Mutat·2009
8-other
The mean anatomical shape of the tibial plateau at the knee arthroplasty resection level: an investigation using MRI.
PMID 19467875·Knee·2009
4-observational
[Genetic causes of hereditary cone and cone-rod dystrophies].
PMID 19184602·Ophthalmologe·2009
6-review
Phenotypic variability and long-term follow-up of patients with known and novel PRPH2/RDS gene mutations.
PMID 19038374·Am J Ophthalmol·2009
8-other
Mutations in CNGA3 impair trafficking or function of cone cyclic nucleotide-gated channels, resulting in achromatopsia.
PMID 18521937·Hum Mutat·2008
8-other
CNGA3 mutations in two United Arab Emirates families with achromatopsia.
PMID 18636117·Mol Vis·2008
8-other
Cone and cone-rod dystrophy segregating in the same pedigree due to the same novel CRX gene mutation.
PMID 18653602·Br J Ophthalmol·2008
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
- 27031 W WARREN ST
DEARBORN HEIGHTS, MI 48127 - Phone
- (313) 274-3320
Quick Facts
- NPI
- 1245229541
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 30
- Publications
- 20
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