Back to Search
ERIN BAUMGARTNER, M.D.
M.D.
Anatomic Pathology & Clinical Pathology Physician
NPI: 1215381611IndividualAccepts Medicare
Specialties, Licenses & Credentials
Anatomic Pathology & Clinical Pathology PhysicianPrimary
Pathology — Anatomic Pathology & Clinical Pathology
Code: 207ZP0102X
D91126(MD)DR.0068693(CO)
CMS Specialties
PrimaryPATHOLOGY
Education
UNIVERSITY OF LOUISVILLE SCHOOL OF MEDICINE
Class of 2016
Research & Publications (20)
Hypothermia and other cold-related morbidity emergency department visits: United States, 1995-2004.
PMID 19099327·Wilderness Environ Med·2008
8-other
Coenzyme Q(10) is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduria.
PMID 19504350·J Inherit Metab Dis·2009
8-other
Long-term outcome in methylmalonic acidurias is influenced by the underlying defect (mut0, mut-, cblA, cblB).
PMID 17597648·Pediatr Res·2007
4-observational
Mutation and biochemical analysis of 19 probands with mut0 and 13 with mut- methylmalonic aciduria: identification of seven novel mutations.
PMID 17113806·Mol Genet Metab·2007
8-other
The first case of 3-methylcrotonyl-CoA carboxylase (MCC) deficiency responsive to biotin.
PMID 16773504·Neuropediatrics·2006
5-case
Severe holocarboxylase synthetase deficiency with incomplete biotin responsiveness resulting in antenatal insult in samoan neonates.
PMID 16027709·J Pediatr·2005
5-case
Pyruvate dehydrogenase phosphatase deficiency: identification of the first mutation in two brothers and restoration of activity by protein complementation.
PMID 15855260·J Clin Endocrinol Metab·2005
8-other
Isolated 3-methylcrotonyl-CoA carboxylase deficiency: evidence for an allele-specific dominant negative effect and responsiveness to biotin therapy.
PMID 15359379·Am J Hum Genet·2004
5-case
Outcome in patients with profound biotinidase deficiency: relevance of newborn screening.
PMID 15230462·Dev Med Child Neurol·2004
8-other
Fibromyalgia: a randomised, controlled trial of a treatment programme based on self management.
PMID 14962965·Ann Rheum Dis·2004
3-trial
Partial response to biotin therapy in a patient with holocarboxylase synthetase deficiency: clinical, biochemical, and molecular genetic aspects.
PMID 12855220·Mol Genet Metab·2003
5-case
Neurophysiologic evidence for a central sensitization in patients with fibromyalgia.
PMID 12746916·Arthritis Rheum·2003
3-trial
Biotin-dependent carboxylase activities in different CNS and skin-derived cells, and their sensitivity to biotin-depletion.
PMID 12214565·Int J Vitam Nutr Res·2002
7-preclinical
Cobalamin disorder Cbl-C presenting with late-onset thrombotic microangiopathy.
PMID 12210350·Am J Med Genet·2002
5-case
A six year prospective study of a cohort of patients with fibromyalgia.
PMID 12079910·Ann Rheum Dis·2002
8-other
Leukodystrophy and CSF purine abnormalities associated with isolated 3-methylcrotonyl-CoA carboxylase deficiency.
PMID 11893004·Metab Brain Dis·2002
5-case
Perioperative management of a child with very-long-chain acyl-coenzyme A dehydrogenase deficiency.
PMID 11882234·Paediatr Anaesth·2002
5-case
Biocytin and biotin uptake into NB2a neuroblastoma and C6 astrocytoma cells.
PMID 11792359·Brain Res·2002
7-preclinical
Biotinidase determination in serum and dried blood spots--high sensitivity fluorimetric ultramicro-assay.
PMID 11718693·Clin Chim Acta·2001
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 3 locations total
- Address
- 4940 Eastern Ave
Baltimore, MD 21224 - Phone
- (410) 955-1180
Quick Facts
- NPI
- 1215381611
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 3
- Years in Practice
- 10
- Publications
- 20
Are you this provider?
Claim Your Profile