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MEREDITH BAUMGARTNER, MD
MD
Family Medicine Physician
NPI: 1407417264IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
036165264(IL)
Education
UNIVERSITY OF ILLINOIS COLLEGE OF MED (CHI/PEOR/ROCK/CHM-URB)
Class of 2019
Research & Publications (20)
Prediction of outcome in isolated methylmalonic acidurias: combined use of clinical and biochemical parameters.
PMID 19642010·J Inherit Metab Dis·2009
4-observational
Molecular mechanism of dominant expression in 3-methylcrotonyl-CoA carboxylase deficiency.
PMID 15868465·J Inherit Metab Dis·2005
6-review
Delta1-pyrroline-5-carboxylate synthase deficiency: neurodegeneration, cataracts and connective tissue manifestations combined with hyperammonaemia and reduced ornithine, citrulline, arginine and proline.
PMID 15517380·Eur J Pediatr·2005
5-case
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
Spatial and temporal distribution of "curvina" larvae (Plagioscion squamosissimus Heckel, 1840) and its relationship to some environmental variables in the Upper Paraná River floodplain, Brazil.
PMID 14758697·Braz J Biol·2003
7-preclinical
Robotic-assisted laparoscopic extended pelvic lymph node dissection for prostate cancer: surgical technique and experience with the first 99 cases.
PMID 19101076·Eur Urol·2009
8-other
Identification of novel mutations in the SLC25A15 gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: a clinical, molecular, and functional study.
PMID 19242930·Hum Mutat·2009
8-other
Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlations.
PMID 19370762·Hum Mutat·2009
4-observational
Cerebral edema and intracranial hypertension in an adult with maple syrup urine disease.
PMID 19364339·Eur J Neurol·2009
5-case
Management and outcome in 75 individuals with long-chain fatty acid oxidation defects: results from a workshop.
PMID 19399638·J Inherit Metab Dis·2009
4-observational
The PDZ protein MPP2 interacts with c-Src in epithelial cells.
PMID 19665017·Exp Cell Res·2009
7-preclinical
Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism.
PMID 19136951·Nat Genet·2009
8-other
Laser fibre deterioration and loss of power output during photo-selective 80-w potassium-titanyl-phosphate laser vaporisation of the prostate.
PMID 18387731·Eur Urol·2009
8-other
Dietary β-hydroxy-β-methylbutyrate supplementation influences performance differently after immunization in broiler chickens.
PMID 18522686·J Anim Physiol Anim Nutr (Berl)·2009
2-rct
3-Methylcrotonyl-CoA carboxylase deficiency: phenotypic variability in a family.
PMID 19339287·J Child Neurol·2009
5-case
Treatment recommendations in long-chain fatty acid oxidation defects: consensus from a workshop.
PMID 19452263·J Inherit Metab Dis·2009
4-observational
Marinamoeba thermophila, a new marine heterolobosean amoeba growing at 50 degrees C.
PMID 19339165·Eur J Protistol·2009
7-preclinical
Recurrent attacks of status epilepticus as predominant symptom in 3-methylcrotonyl-CoA carboxylase deficiency.
PMID 17869468·Brain Dev·2008
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
- 2750 W NORTH AVE
CHICAGO, IL 60647 - Phone
- (312) 666-3494
Quick Facts
- NPI
- 1407417264
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 7
- Publications
- 20
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