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BARBARA BURTON, MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1699743088Individual
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
Research & Publications (20)
Home infusion therapy is safe and enhances compliance in patients with mucopolysaccharidoses.
PMID 19427803·Mol Genet Metab·2009
3-trial
The response of patients with phenylketonuria and elevated serum phenylalanine to treatment with oral sapropterin dihydrochloride (6R-tetrahydrobiopterin): a phase II, multicentre, open-label, screening study.
PMID 17846916·J Inherit Metab Dis·2007
3-trial
Lesion of the ventral and intermediate hippocampus abolishes anticipatory activity in the medial prefrontal cortex of the rat.
PMID 19103227·Behav Brain Res·2009
7-preclinical
Efficacy of sapropterin dihydrochloride in increasing phenylalanine tolerance in children with phenylketonuria: a phase III, randomized, double-blind, placebo-controlled study.
PMID 19261295·J Pediatr·2009
3-trial
Acute central retinal artery occlusion presenting as CREST syndrome: a case report.
PMID 19123948·Cases J·2009
8-other
Mutation in BAG3 causes severe dominant childhood muscular dystrophy.
PMID 19085932·Ann Neurol·2009
7-preclinical
A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency.
PMID 19157942·Mol Genet Metab·2009
6-review
5-Aminopyrimidin-2-ylnitriles as cathepsin K inhibitors.
PMID 19231183·Bioorg Med Chem Lett·2009
8-other
Development of theta rhythmicity in entorhinal stellate cells of the juvenile rat.
PMID 18829850·J Neurophysiol·2008
7-preclinical
Iatrogenic retinal detachment due to cannula slippage despite use of luer-lock syringe system.
PMID 18721732·J Cataract Refract Surg·2008
8-other
SpoIIIE strips proteins off the DNA during chromosome translocation.
PMID 18593879·Genes Dev·2008
8-other
Safety and efficacy of 22 weeks of treatment with sapropterin dihydrochloride in patients with phenylketonuria.
PMID 18932221·Am J Med Genet A·2008
4-observational
Molecular and clinical genetics of mitochondrial diseases due to POLG mutations.
PMID 18546365·Hum Mutat·2008
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
- 2300 CHILDREN'S PLAZA, CHILDREN'S MEMORIAL HOSPITAL, GENETICS #59
CHICAGO, IL 60614 - Phone
- (773) 880-4462
Quick Facts
- NPI
- 1699743088
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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