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BURNETTA HERRON M.D.
M.D.
Surgery Physician
NPI: 1841211513IndividualAccepts Medicare
Specialties, Licenses & Credentials
Surgery PhysicianPrimary
Surgery
Code: 208600000X
036-101632(IL)
Education
UNIVERSITY OF TEXAS MEDICAL BRANCH AT GALVESTON
Class of 1997
Research & Publications (20)
THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia.
PMID 18327258·Nat Genet·2008
7-preclinical
Dissociation of seizure traits in inbred strains of mice using the flurothyl kindling model of epileptogenesis.
PMID 18950623·Exp Neurol·2009
7-preclinical
"In the know" with centers for Medicare and Medicaid services changes.
PMID 18172949·Prog Cardiovasc Nurs·2007
8-other
Localization of two new X-linked quantitative trait loci controlling corpus callosum size in the mouse.
PMID 16899052·Genes Brain Behav·2007
4-observational
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
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
Paraganglioma of the cauda equina with subarachnoid haemorrhage.
PMID 17293223·Clin Radiol·2007
5-case
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
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
Genomics of the future: identification of quantitative trait loci in the mouse.
PMID 16339372·Genome Res·2005
6-review
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
Via practice · 4 locations total
- Address
- 1500 S Fairfield Ave Dept Of
Chicago, IL 60608 - Phone
- (312) 257-4752
Quick Facts
- NPI
- 1841211513
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 4
- Years in Practice
- 29
- Publications
- 20
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