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MICHELYN PATTON, PHARMD
PHARMD
Pharmacist
NPI: 1932512548Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
E13374(MS)
Research & Publications (20)
Infection with community-onset Staphylococcus aureus and influenza virus in hospitalized children.
PMID 19478685·Pediatr Infect Dis J·2009
8-other
15q overgrowth syndrome: a newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q.
PMID 19133692·Am J Med Genet A·2009
8-other
Elements of morphology: standard terminology for the nose and philtrum.
PMID 19152422·Am J Med Genet A·2009
8-other
"I was never like that": Australian findings on the psychological and psychiatric sequelae of corticosteroids in haematology treatments.
PMID 18478273·Support Care Cancer·2009
8-other
Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasia.
PMID 19250384·Clin Genet·2009
5-case
Homozygous mutation of desmocollin-2 in arrhythmogenic right ventricular cardiomyopathy with mild palmoplantar keratoderma and woolly hair.
PMID 18957847·Cardiology·2009
5-case
A mutation in NFkappaB interacting protein 1 causes cardiomyopathy and woolly haircoat syndrome of Poll Hereford cattle.
PMID 19016676·Anim Genet·2009
7-preclinical
Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration.
PMID 18252231·Am J Hum Genet·2008
4-observational
Levels of systemic metal ions in patients with intramedullary nails.
PMID 19085501·Acta Orthop·2008
8-other
Ruptured cerebral aneurysm in a patient with Floating-Harbor syndrome.
PMID 18978661·Clin Dysmorphol·2008
5-case
DNA microarray analysis of the heat shock transcriptome of the obligate intracytoplasmic pathogen Rickettsia prowazekii.
PMID 18952868·Appl Environ Microbiol·2008
7-preclinical
Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the Amish.
PMID 18467358·Heart·2008
8-other
A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23.
PMID 18463364·Neurology·2008
8-other
Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development.
PMID 17924334·Am J Hum Genet·2007
7-preclinical
Prevalence and clinical significance of cardiovascular abnormalities in patients with the LEOPARD syndrome.
PMID 17697839·Am J Cardiol·2007
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2310 CLAY ST
VICKSBURG, MS 39183 - Phone
- (601) 661-5856
Quick Facts
- NPI
- 1932512548
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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