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AARON SHARP, MD
MD
Family Medicine Physician
NPI: 1215432935IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
ME151872(FL)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
OTHER
Class of 2017
Research & Publications (20)
First-in-man case report of the use of an Edwards-Sapien valve to treat a regurgitant CoreValve aortic valve prosthesis.
PMID 19642192·Catheter Cardiovasc Interv·2010
5-case
The 2009 European Society of Human Genetics Meeting: novel technologies driving change.
PMID 19591664·Genome Med·2009
8-other
In vivo penetration mechanics and mechanical properties of mouse brain tissue at micrometer scales.
PMID 19224718·IEEE Trans Biomed Eng·2009
7-preclinical
Pharmacokinetics and pharmacodynamics of a novel triazole, isavuconazole: mathematical modeling, importance of tissue concentrations, and impact of immune status on antifungal effect.
PMID 19451288·Antimicrob Agents Chemother·2009
7-preclinical
Comparison of VerifyNow-P2Y12 test and Flow Cytometry for monitoring individual platelet response to clopidogrel. What is the cut-off value for identifying patients who are low responders to clopidogrel therapy?
PMID 19419580·Thromb J·2009
8-other
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy.
PMID 19136953·Nat Genet·2009
8-other
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.
PMID 19372089·J Med Genet·2009
8-other
Efficacy of isavuconazole, voriconazole and fluconazole in temporarily neutropenic murine models of disseminated Candida tropicalis and Candida krusei.
PMID 19008255·J Antimicrob Chemother·2009
7-preclinical
Emerging themes and new challenges in defining the role of structural variation in human disease.
PMID 18837009·Hum Mutat·2009
6-review
Investigation of immunosuppressive mechanisms in a mouse glioma model.
PMID 19430886·J Neurooncol·2009
7-preclinical
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.
PMID 18550696·J Med Genet·2009
8-other
Ethnicity and left ventricular diastolic function in hypertension an ASCOT (Anglo-Scandinavian Cardiac Outcomes Trial) substudy.
PMID 18786484·J Am Coll Cardiol·2008
3-trial
CNVs and genetic medicine (excitement and consequences of a rediscovery).
PMID 19287134·Cytogenet Genome Res·2008
6-review
P2x7 deficiency suppresses development of experimental autoimmune encephalomyelitis.
PMID 18691411·J Neuroinflammation·2008
7-preclinical
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.
PMID 18628315·J Med Genet·2008
8-other
Potocki-Lupski syndrome mimicking a connective tissue disorder.
PMID 18541972·Clin Dysmorphol·2008
5-case
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
PMID 18784092·N Engl J Med·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
- 1760 EDGEWOOD AVE W
JACKSONVILLE, FL 32208 - Phone
- (940) 358-8480
Quick Facts
- NPI
- 1215432935
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 9
- Publications
- 20
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