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KELLY POIRIER, D.O.
D.O.
Surgery Physician
NPI: 1952835589IndividualAccepts Medicare
Specialties, Licenses & Credentials
Surgery PhysicianPrimary
Surgery
Code: 208600000X
OT017711(PA)25MB11979500(NJ)
CMS Specialties
PrimaryGENERAL SURGERY
Education
OTHER
Class of 2017
Research & Publications (20)
Combination of infantile spasms, non-epileptic seizures and complex movement disorder: a new case of ARX-related epilepsy.
PMID 18468866·Epilepsy Res·2008
5-case
Escherichia coli O157:H7 survives within human macrophages: global gene expression profile and involvement of the Shiga toxins.
PMID 18725421·Infect Immun·2008
8-other
Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A).
PMID 17584854·Hum Mutat·2007
8-other
Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosis.
PMID 16235064·Neurogenetics·2006
7-preclinical
Maternal mosaicism for mutations in the ARX gene in a family with X linked mental retardation.
PMID 16078051·Hum Genet·2005
8-other
Neuroanatomical distribution of ARX in brain and its localisation in GABAergic neurons.
PMID 14992814·Brain Res Mol Brain Res·2004
4-observational
Loss of parental-specific methylation at the IGF2 locus in human hepatocellular carcinoma.
PMID 14595760·J Pathol·2003
8-other
Epileptic encephalopathy in a girl with an interstitial deletion of Xp22 comprising promoter and exon 1 of the CDKL5 gene.
PMID 19455595·Am J Med Genet B Neuropsychiatr Genet·2010
5-case
Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria.
PMID 19465910·Nat Genet·2009
8-other
Are all models created equal? A content analysis of women in advertisements of fitness versus fashion magazines.
PMID 19237328·Body Image·2009
8-other
Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females.
PMID 19214208·PLoS Genet·2009
8-other
[Epileptogenic brain malformations: radiological and clinical presentation and indications for genetic testing].
PMID 18808783·Rev Neurol (Paris)·2008
6-review
Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations.
PMID 18728072·J Med Genet·2008
8-other
Detection of exonic copy-number changes using a highly efficient oligonucleotide-based comparative genomic hybridization-array method.
PMID 18683213·Hum Mutat·2008
8-other
Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A.
PMID 18669490·Brain·2008
5-case
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans.
PMID 17218254·Cell·2007
7-preclinical
Contribution of the stg fimbrial operon of Salmonella enterica serovar Typhi during interaction with human cells.
PMID 17709421·Infect Immun·2007
8-other
Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia.
PMID 17617514·J Med Genet·2007
5-case
Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium.
PMID 17221867·Hum Mutat·2007
8-other
The ARX mutations: a frequent cause of X-linked mental retardation.
PMID 16523516·Am J Med Genet A·2006
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
- 4301 W MARKHAM ST
LITTLE ROCK, AR 72205 - Phone
- (501) 686-6627
Quick Facts
- NPI
- 1952835589
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 9
- Publications
- 20
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