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LINA MEHTA, MD
MD
Nuclear Radiology Physician
NPI: 1467470666Individual
Specialties, Licenses & Credentials
Nuclear Radiology PhysicianPrimary
Radiology — Nuclear Radiology
Code: 2085N0904X
35074497(OH)
Research & Publications (20)
Proof of concept studies for tissue-protective agents in multiple sclerosis.
PMID 19389749·Mult Scler·2009
6-review
Clinical outcomes after long-term treatment with alglucosidase alfa in infants and children with advanced Pompe disease.
PMID 19287243·Genet Med·2009
3-trial
Polyunsaturated fatty acids and their potential therapeutic role in multiple sclerosis.
PMID 19194388·Nat Clin Pract Neurol·2009
6-review
Ovotesticular disorder of sexual development (true hermaphroditism).
PMID 18822450·Urology·2009
5-case
Sporadic fatal insomnia masquerading as a paraneoplastic cerebellar syndrome.
PMID 18625868·Arch Neurol·2008
5-case
Vascular endothelial growth factor-165 gene therapy promotes cardiomyogenesis in reperfused myocardial infarction.
PMID 18422517·J Interv Cardiol·2008
7-preclinical
Neuromyelitis optica spectrum disorder in a patient with systemic lupus erythematosus and anti-phospholipid antibody syndrome.
PMID 18208886·Mult Scler·2008
5-case
Impact of body mass index on outcomes after percutaneous coronary intervention in patients with acute myocardial infarction.
PMID 17398181·Am J Cardiol·2007
8-other
Lung cancer screening as a teachable moment for smoking cessation.
PMID 17196298·Lung Cancer·2007
8-other
Fatal granulomatous Acanthamoeba encephalitis mimicking a stroke, diagnosed by correlation of results of sequential magnetic resonance imaging, biopsy, in vitro culture, immunofluorescence analysis, and molecular analysis.
PMID 16988022·J Clin Microbiol·2006
7-preclinical
Evaluation of oxacillin and cefoxitin disk diffusion test for routine detection of methicillin resistant Staphylococcus aureus.
PMID 16380800·Saudi Med J·2005
8-other
Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genes.
PMID 15820313·Genomics·2005
4-observational
Rationale and study design of the CardioGene Study: genomics of in-stent restenosis.
PMID 15469413·Pharmacogenomics·2004
8-other
Clinical and molecular delineation of the Greig cephalopolysyndactyly contiguous gene deletion syndrome and its distinction from acrocallosal syndrome.
PMID 14608643·Am J Med Genet A·2003
4-observational
Dual derivatization and GC-MS analysis of phenolic compounds suspected of being xenoestrogens.
PMID 12716065·J Environ Sci Health A Tox Hazard Subst Environ Eng·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
- 11100 EUCLID AVENUE
CLEVELAND, OH 44106 - Phone
- (216) 844-1700
Quick Facts
- NPI
- 1467470666
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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