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ALI SHARP, DO
DO
Student in an Organized Health Care Education/Training Program
NPI: 1346826757Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
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
- 744 W 9TH ST
TULSA, OK 74127 - Phone
- (918) 599-1000
Quick Facts
- NPI
- 1346826757
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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