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DANA BEESON, DO
DO
Internal Medicine Physician
NPI: 1689069809IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
C2-0013116(DE)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
PHILADELPHIA COLLEGE OF OSTEOPATHIC MEDICINE
Class of 2015
Research & Publications (20)
Egg harvesting for stem cell research: medical risks and ethical problems.
PMID 17007682·Reprod Biomed Online·2006
6-review
Social and ethical challenges of prenatal diagnosis.
PMID 15782442·Med Ethics (Burlingt Mass)·2000
8-other
Germline mutation in DOK7 associated with fetal akinesia deformation sequence.
PMID 19261599·J Med Genet·2009
8-other
Assessing the relationship between laboratory whole effluent toxicity test data and in-stream biological communities.
PMID 19009223·Bull Environ Contam Toxicol·2009
7-preclinical
AChR deficiency due to epsilon-subunit mutations: two common mutations in the Netherlands.
PMID 19544078·J Neurol·2009
8-other
IgG1 antibodies to acetylcholine receptors in 'seronegative' myasthenia gravis.
PMID 18515870·Brain·2008
8-other
Myasthenia gravis seronegative for acetylcholine receptor antibodies.
PMID 18567857·Ann N Y Acad Sci·2008
7-preclinical
Congenital myasthenic syndromes and the formation of the neuromuscular junction.
PMID 18567858·Ann N Y Acad Sci·2008
7-preclinical
Aquaporin-4 antibodies in neuromyelitis optica and longitudinally extensive transverse myelitis.
PMID 18625857·Arch Neurol·2008
4-observational
Preferential expression of AChR epsilon-subunit in thymomas from patients with myasthenia gravis.
PMID 18657869·J Neuroimmunol·2008
8-other
Mutation analysis of CHRNA1, CHRNB1, CHRND, and RAPSN genes in multiple pterygium syndrome/fetal akinesia patients.
PMID 18179903·Am J Hum Genet·2008
8-other
Mutations causing DOK7 congenital myasthenia ablate functional motifs in Dok-7.
PMID 18165682·J Biol Chem·2008
7-preclinical
Congenital myasthenic syndromes in childhood: diagnostic and management challenges.
PMID 18707767·J Neuroimmunol·2008
8-other
Phenotypical spectrum of DOK7 mutations in congenital myasthenic syndromes.
PMID 17439981·Brain·2007
8-other
Hairpin DNAzymes: a new tool for efficient cellular gene silencing.
PMID 17582227·J Gene Med·2007
8-other
An IRF8-binding promoter variant and AIRE control CHRNA1 promiscuous expression in thymus.
PMID 17687331·Nature·2007
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
- 4755 OGLETOWN STANTON RD
NEWARK, DE 19718 - Phone
- (302) 733-1042
Quick Facts
- NPI
- 1689069809
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 11
- Publications
- 20
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