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BRYAN HERRON, MD
MD
Orthopaedic Surgery Physician
NPI: 1245252311IndividualAccepts Medicare
Specialties, Licenses & Credentials
Orthopaedic Surgery PhysicianPrimary
Orthopaedic Surgery
Code: 207X00000X
D51875(MD)
CMS Specialties
PrimaryORTHOPEDIC SURGERY
Education
TUFTS UNIVERSITY SCHOOL OF MEDICINE
Class of 1988
Research & Publications (20)
Dissociation of seizure traits in inbred strains of mice using the flurothyl kindling model of epileptogenesis.
PMID 18950623·Exp Neurol·2009
7-preclinical
THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia.
PMID 18327258·Nat Genet·2008
7-preclinical
Unusual late development of dopamine agonist resistance in two women with hyperprolactinaemia associated with transition from micro to macroadenoma.
PMID 17201816·Clin Endocrinol (Oxf)·2007
5-case
Absence of aquaporin-4 expression in lesions of neuromyelitis optica but increased expression in multiple sclerosis lesions and normal-appearing white matter.
PMID 17143632·Acta Neuropathol·2007
4-observational
Localization of two new X-linked quantitative trait loci controlling corpus callosum size in the mouse.
PMID 16899052·Genes Brain Behav·2007
4-observational
Paraganglioma of the cauda equina with subarachnoid haemorrhage.
PMID 17293223·Clin Radiol·2007
5-case
"In the know" with centers for Medicare and Medicaid services changes.
PMID 18172949·Prog Cardiovasc Nurs·2007
8-other
Impact of the implementation of telemanagement on a disease management program in an elderly heart failure cohort.
PMID 18059196·Prog Cardiovasc Nurs·2007
8-other
Benign signet ring cells in the subserosa of the small intestine: a pseudoneoplastic phenomenon.
PMID 16457415·Ulster Med J·2006
5-case
Genomics of the future: identification of quantitative trait loci in the mouse.
PMID 16339372·Genome Res·2005
6-review
A mutation in stratifin is responsible for the repeated epilation (Er) phenotype in mice.
PMID 16200063·Nat Genet·2005
4-observational
Fog2 is required for normal diaphragm and lung development in mice and humans.
PMID 16103912·PLoS Genet·2005
8-other
A mutation in NFkB interacting protein 1 results in cardiomyopathy and abnormal skin development in wa3 mice.
PMID 15661756·Hum Mol Genet·2005
7-preclinical
Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis.
PMID 11818962·Nat Genet·2002
7-preclinical
Anomalous asymmetry of fusiform and parahippocampal gyrus gray matter in schizophrenia: A postmortem study.
PMID 10618011·Am J Psychiatry·2000
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 497 MAIN ST, STE 200
PRINCE FREDERICK, MD 20678 - Phone
- (410) 414-9840
Quick Facts
- NPI
- 1245252311
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 38
- Publications
- 20
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