Back to Search
ERIN TREACY, M.D.
M.D.
Anesthesiology Physician
NPI: 1972821981IndividualAccepts Medicare
Specialties, Licenses & Credentials
Anesthesiology PhysicianPrimary
Anesthesiology
Code: 207L00000X
D88260(MD)
CMS Specialties
PrimaryANESTHESIOLOGY
Education
UNIVERSITY OF MARYLAND SCHOOL OF MEDICINE
Class of 2010
Research & Publications (20)
Negative screening tests in classical galactosaemia caused by S135L homozygosity.
PMID 19418241·J Inherit Metab Dis·2009
5-case
Incidence and prevalence of mucopolysaccharidosis type 1 in the Irish republic.
PMID 18463126·Arch Dis Child·2009
4-observational
Further pitfalls in the diagnosis of mtDNA mutations: homoplasmic mt-tRNA mutations.
PMID 18178636·J Med Genet·2008
8-other
Sensory-motor polyneuropathy occurring in variant maple syrup urine disease.
PMID 18855118·J Inherit Metab Dis·2008
5-case
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
Reversible multiorgan system involvement in a neonate with complex IV deficiency.
PMID 18940565·Pediatr Neurol·2008
5-case
Long chain fatty acid oxidation defects in children: importance of detection and treatment options.
PMID 17431731·Ir J Med Sci·2007
5-case
Mitochondrial cytopathies, phenotypic heterogeneity and a high incidence.
PMID 17144232·Ir Med J·2006
8-other
Polymorphisms of the Flavin containing monooxygenase 3 (FMO3) gene do not predispose to essential hypertension in Caucasians.
PMID 16324215·BMC Med Genet·2005
8-other
Fatal presentation of ornithine transcarbamylase deficiency in a 62-year-old man and family studies.
PMID 15243986·J Inherit Metab Dis·2004
5-case
Neonatal seizures and limb malformations associated with liver-specific complex IV respiratory chain deficiency.
PMID 15023375·Eur J Paediatr Neurol·2004
5-case
Coats' plus: a progressive familial syndrome of bilateral Coats' disease, characteristic cerebral calcification, leukoencephalopathy, slow pre- and post-natal linear growth and defects of bone marrow and integument.
PMID 15002047·Neuropediatrics·2004
5-case
Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype.
PMID 12872844·J Inherit Metab Dis·2003
5-case
Genetic diversity within the R408W phenylketonuria mutation lineages in Europe.
PMID 12655548·Hum Mutat·2003
4-observational
In vivo variability of TMA oxidation is partially mediated by polymorphisms of the FMO3 gene.
PMID 11461189·Mol Genet Metab·2001
8-other
A novel deletion in the flavin-containing monooxygenase gene (FMO3) in a Greek patient with trimethylaminuria.
PMID 11266081·Pharmacogenetics·2001
5-case
Fenofibrate raises plasma homocysteine levels in the fasted and fed states.
PMID 11254917·Atherosclerosis·2001
3-trial
Variable onset of metachromatic leukodystrophy in a Vietnamese family.
PMID 11020646·Pediatr Neurol·2000
5-case
Short-chain hydroxyacyl-coenzyme A dehydrogenase deficiency presenting as unexpected infant death: A family study.
PMID 10931422·J Pediatr·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 22 S GREENE ST
BALTIMORE, MD 21201 - Phone
- (667) 214-1616
Quick Facts
- NPI
- 1972821981
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 16
- Publications
- 20
Are you this provider?
Claim Your Profile