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DWIGHT BENN, MD
MD
Internal Medicine Physician
NPI: 1487767547IndividualAccepts Medicare
Specialties, Licenses & Credentials
Hospitalist Physician
Hospitalist
Code: 208M00000X
200401616(NC)
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
200401616(NC)
Education
STATE UNIVERSITY OF NY UPSTATE MEDICAL UNIVERSITY
Class of 2002
Research & Publications (20)
Genetic testing in pheochromocytoma- and paraganglioma-associated syndromes.
PMID 17102077·Ann N Y Acad Sci·2006
6-review
Genetic basis of phaeochromocytoma and paraganglioma.
PMID 16980204·Best Pract Res Clin Endocrinol Metab·2006
6-review
Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.
PMID 16317055·J Clin Endocrinol Metab·2006
8-other
Professional monopoly, social covenant, and access to oral health care in the United States.
PMID 14587672·J Dent Educ·2003
8-other
Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas.
PMID 12618761·Oncogene·2003
8-other
Applying evidence-based dentistry to caries management in dental practice: a computerized approach.
PMID 12462699·J Am Dent Assoc·2002
8-other
Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1p.
PMID 11156410·Cancer Res·2000
8-other
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
Microarray gene expression and immunohistochemistry analyses of adrenocortical tumors identify IGF2 and Ki-67 as useful in differentiating carcinomas from adenomas.
PMID 19218281·Endocr Relat Cancer·2009
4-observational
Denaturing high performance liquid chromatography detection of SDHB, SDHD, and VHL germline mutations in pheochromocytoma.
PMID 19215943·J Surg Res·2009
8-other
Paediatric bilateral adrenal phaeochromocytomas in association with a novel mutation in the von Hippel Lindau gene.
PMID 18928468·J Paediatr Child Health·2008
5-case
Characterization of differentiated quiescent and nonquiescent cells in yeast stationary-phase cultures.
PMID 18199684·Mol Biol Cell·2008
8-other
Loss of heterozygosity of 17p13, with possible involvement of ACADVL and ALOX15B, in the pathogenesis of adrenocortical tumors.
PMID 18156936·Ann Surg·2008
8-other
Gastrointestinal stromal tumour in succinate dehydrogenase subunit B mutation-associated familial phaeochromocytoma/paraganglioma.
PMID 16916404·ANZ J Surg·2006
5-case
Isolation of quiescent and nonquiescent cells from yeast stationary-phase cultures.
PMID 16818721·J Cell Biol·2006
4-observational
Comorbid oppositional defiant disorder and the risk of relapse during 9 months of atomoxetine treatment for attention-deficit/hyperactivity disorder.
PMID 16523251·Eur Child Adolesc Psychiatry·2006
2-rct
An apparently sporadic paraganglioma with an SDHB gene germline mutation presenting at age 68 years.
PMID 16472267·Intern Med J·2006
5-case
A HIF1alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas.
PMID 16103922·PLoS Genet·2005
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 5 locations total
- Address
- 2001 VAIL AVE
CHARLOTTE, NC 28207 - Phone
- (704) 304-6070
Locations (5)
Practice Location
2001 VAIL AVE, CHARLOTTE, NC
(704) 304-6070
Practice Location
1000 BLYTHE BLVD, CHARLOTTE, NC
(704) 355-0720
Practice Location
10628 PARK RD, CHARLOTTE, NC
(704) 667-7070
Practice Location
8800 N TRYON ST, CHARLOTTE, NC
(704) 863-6241
Practice Location
433 MCALISTER RD, LINCOLNTON, NC
(704) 574-4746
Quick Facts
- NPI
- 1487767547
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 5
- Years in Practice
- 24
- Publications
- 20
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