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MARK MURESAN, M.D.
M.D.
Pediatrics Physician
NPI: 1356326268Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
35-06-7171(OH)
Research & Publications (15)
Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out.
PMID 19351833·Cancer Res·2009
8-other
Mutations in NR5A1 associated with ovarian insufficiency.
PMID 19246354·N Engl J Med·2009
7-preclinical
Breast-conserving treatment in the elderly: long-term results of adjuvant hypofractionated and normofractionated radiotherapy.
PMID 19168297·Int J Radiat Oncol Biol Phys·2009
8-other
Dominant-negative GCMB mutations cause an autosomal dominant form of hypoparathyroidism.
PMID 18583467·J Clin Endocrinol Metab·2008
5-case
Bone metastases from differentiated thyroid carcinoma.
PMID 18310274·Endocr Relat Cancer·2008
6-review
Anti-inflammatory effect of antidiabetic thiazolidinediones prevents bone resorption rather than cartilage changes in experimental polyarthritis.
PMID 18199331·Arthritis Res Ther·2008
4-observational
Identification of potential gene markers and insights into the pathophysiology of pheochromocytoma malignancy.
PMID 17878247·J Clin Endocrinol Metab·2007
8-other
Development of novel tools for the diagnosis and prognosis of pheochromocytoma using peptide marker immunoassay and gene expression profiling approaches.
PMID 17102122·Ann N Y Acad Sci·2006
8-other
Expression and processing of the neuroendocrine protein secretogranin II in benign and malignant pheochromocytomas.
PMID 17102121·Ann N Y Acad Sci·2006
8-other
Recombinant human thyrotropin stimulates thyroid angiogenesis in vivo.
PMID 16839254·Thyroid·2006
7-preclinical
Lack of association between microsatellite instability and benign adrenal tumors.
PMID 16715450·World J Surg·2006
8-other
Circulating EM66 is a highly sensitive marker for the diagnosis and follow-up of pheochromocytoma.
PMID 16287097·Int J Cancer·2006
8-other
Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene.
PMID 16249420·JAMA·2005
4-observational
[Endocrine tumors of the gastro-intestinal tract (Carcinoid tumors)].
PMID 15581816·Ann Chir·2004
6-review
Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations.
PMID 15328326·JAMA·2004
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
- 5510 NIKE DR
HILLIARD, OH 43026 - Phone
- (614) 529-4260
Quick Facts
- NPI
- 1356326268
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 15
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