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VERONICA PRATT, MD
MD
Family Medicine Physician
NPI: 1528028008Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
MD063162L(PA)
Research & Publications (18)
Alterations in lymphocyte function and relation to phospholipid composition after burn injury in humans.
PMID 12163788·Crit Care Med·2002
4-observational
Plasma and neutrophil fatty acid composition in advanced cancer patients and response to fish oil supplementation.
PMID 12454764·Br J Cancer·2002
3-trial
Fatty acid content of plasma lipids and erythrocyte phospholipids are altered following burn injury.
PMID 11521965·Lipids·2001
8-other
Identification of cystic fibrosis variants by polymerase chain reaction/oligonucleotide ligation assay.
PMID 19324992·J Mol Diagn·2009
8-other
The interface of Medicare coverage decision-making and emerging molecular-based laboratory testing.
PMID 19282775·Genet Med·2009
8-other
Clinician perspectives about molecular genetic testing for heritable conditions and development of a clinician-friendly laboratory report.
PMID 19197001·J Mol Diagn·2009
8-other
CpG methylation analysis--current status of clinical assays and potential applications in molecular diagnostics: a report of the Association for Molecular Pathology.
PMID 19541921·J Mol Diagn·2009
8-other
Development of genomic reference materials for cystic fibrosis genetic testing.
PMID 19359498·J Mol Diagn·2009
8-other
Consensus characterization of 16 FMR1 reference materials: a consortium study.
PMID 18165276·J Mol Diagn·2008
8-other
Development of a web-based query tool for quality assurance of clinical molecular genetic test results.
PMID 17251341·J Mol Diagn·2007
8-other
Developing a sustainable process to provide quality control materials for genetic testing.
PMID 16247292·Genet Med·2005
6-review
Genetically characterized positive control cell lines derived from residual clinical blood samples.
PMID 16166172·Clin Chem·2005
4-observational
Detection of 677CT/1298AC "double variant" chromosomes: implications for interpretation of MTHFR genotyping results.
PMID 15834246·Genet Med·2005
4-observational
Bioelectronic sensor technology for detection of cystic fibrosis and hereditary hemochromatosis mutations.
PMID 14632577·Arch Pathol Lab Med·2003
8-other
Fluorescent, multiplexed, automated, primer-extension assay for 3120+1G-->A and I148T mutations in cystic fibrosis.
PMID 11673382·Clin Chem·2001
8-other
Biophysical characteristics of anti-Gal(alpha)1-3Gal IgM binding to cell surfaces: implications for xenotransplantation.
PMID 11233908·Transplantation·2001
7-preclinical
Additional copies of the proteolipid protein gene causing Pelizaeus-Merzbacher disease arise by separate integration into the X chromosome.
PMID 10827108·Am J Hum Genet·2000
5-case
Glutamine and arginine: immunonutrients for improved health.
PMID 10910294·Med Sci Sports Exerc·2000
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 400 OXFORD DR, SUITE 202
MONROEVILLE, PA 15146 - Phone
- (412) 380-5040
Quick Facts
- NPI
- 1528028008
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 18
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