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SCOTT KOHL, DO
DO
Emergency Medicine Physician
NPI: 1386640282Individual
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
OS8527(FL)
Research & Publications (20)
The mean anatomical shape of the tibial plateau at the knee arthroplasty resection level: an investigation using MRI.
PMID 19467875·Knee·2009
4-observational
Mutations in the GUCA1A gene involved in hereditary cone dystrophies impair calcium-mediated regulation of guanylate cyclase.
PMID 19459154·Hum Mutat·2009
8-other
Consecutive thermal H2 and light-induced O2 evolution from water promoted by a metal complex.
PMID 19342584·Science·2009
8-other
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
[Genetic causes of hereditary cone and cone-rod dystrophies].
PMID 19184602·Ophthalmologe·2009
6-review
Chondroid metaplasia mimicking recurrent squamous cell carcinoma of the head and neck.
PMID 19172559·Ear Nose Throat J·2009
5-case
An aluminium mold for intraoperative production of antibiotic-loaded PMMA knee prostheses.
PMID 19424917·Acta Orthop·2009
8-other
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
Mutation analysis identifies GUCY2D as the major gene responsible for autosomal dominant progressive cone degeneration.
PMID 18487367·Invest Ophthalmol Vis Sci·2008
4-observational
Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.
PMID 18235024·Invest Ophthalmol Vis Sci·2008
8-other
ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies.
PMID 18285826·Eur J Hum Genet·2008
8-other
Functional analysis of human CNGA3 mutations associated with colour blindness suggests impaired surface expression of channel mutants A3(R427C) and A3(R563C).
PMID 18445228·Eur J Neurosci·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
- 1611 NW 12TH AVE
MIAMI, FL 33136 - Phone
- (954) 709-0966
Quick Facts
- NPI
- 1386640282
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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