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MICHAEL BUTLER, MD
MD
Neurology Physician
NPI: 1477113546IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
2019021199(MO)
CMS Specialties
PrimaryNEUROLOGY
Education
UNIVERSITY OF OKLAHOMA COLLEGE OF MEDICINE
Class of 2019
Research & Publications (20)
Variability in small airway epithelial gene expression among normal smokers.
PMID 18339782·Chest·2008
3-trial
Close relationship of RNase P RNA in Gemmata and anammox planctomycete bacteria.
PMID 17328750·FEMS Microbiol Lett·2007
8-other
Plasma obestatin and ghrelin levels in subjects with Prader-Willi syndrome.
PMID 17304548·Am J Med Genet A·2007
4-observational
Energy expenditure and physical activity in Prader-Willi syndrome: comparison with obese subjects.
PMID 17103434·Am J Med Genet A·2007
4-observational
X-chromosome inactivation patterns in females with Prader-Willi syndrome.
PMID 17036338·Am J Med Genet A·2007
4-observational
C-reactive protein levels in subjects with Prader-Willi syndrome and obesity.
PMID 16617245·Genet Med·2006
8-other
Elafin prevents lipopolysaccharide-induced AP-1 and NF-kappaB activation via an effect on the ubiquitin-proteasome pathway.
PMID 16980310·J Biol Chem·2006
8-other
X chromosome gene expression in human tissues: male and female comparisons.
PMID 16949791·Genomics·2006
4-observational
Management of obesity in Prader-Willi syndrome.
PMID 17082801·Nat Clin Pract Endocrinol Metab·2006
8-other
Pellino3 is a novel upstream regulator of p38 MAPK and activates CREB in a p38-dependent manner.
PMID 15917247·J Biol Chem·2005
7-preclinical
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.
PMID 15805158·J Med Genet·2005
5-case
Plasma peptide YY and ghrelin levels in infants and children with Prader-Willi syndrome.
PMID 15506676·J Pediatr Endocrinol Metab·2004
4-observational
Comparative analysis of ribonuclease P RNA of the planctomycetes.
PMID 15280311·Int J Syst Evol Microbiol·2004
8-other
Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy.
PMID 14993551·Pediatrics·2004
8-other
Dissection of tumor-necrosis factor-alpha inhibition of long-term potentiation (LTP) reveals a p38 mitogen-activated protein kinase-dependent mechanism which maps to early-but not late-phase LTP.
PMID 14980382·Neuroscience·2004
4-observational
Deletion of scbA enhances antibiotic production in Streptomyces lividans.
PMID 12764566·Appl Microbiol Biotechnol·2003
8-other
Imprinting disorders: non-Mendelian mechanisms affecting growth.
PMID 12510981·J Pediatr Endocrinol Metab·2002
6-review
Molecular and ultrastructural confirmation of classification of ATCC 35122 as a strain of Pirellula staleyi.
PMID 12361271·Int J Syst Evol Microbiol·2002
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 · 2 locations total
- Address
- 1 Barnes Jewish Hospital Plz # 90-29928
Saint Louis, MO 63110 - Phone
- (314) 362-1935
Quick Facts
- NPI
- 1477113546
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 2
- Years in Practice
- 7
- Publications
- 20
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