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KATHERINE BEYER, DO
DO
Student in an Organized Health Care Education/Training Program
NPI: 1891444261Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Hypertension and intra-operative incidents: a multicentre study of 125,000 surgical procedures in Swiss hospitals.
PMID 19413818·Anaesthesia·2009
4-observational
Phase diagrams and water activities of aqueous dicarboxylic acid systems of atmospheric importance.
PMID 18959391·J Phys Chem A·2008
8-other
Mediator subunit MED28 (Magicin) is a repressor of smooth muscle cell differentiation.
PMID 17848560·J Biol Chem·2007
7-preclinical
Hypoallergenicity: a principle for the treatment of food allergy.
PMID 17245089·Nestle Nutr Workshop Ser Pediatr Program·2007
6-review
Mechanistic aspects of Parkinson's disease: alpha-synuclein and the biomembrane.
PMID 17652776·Cell Biochem Biophys·2007
6-review
Experimental determination of the H2SO4/(NH4)2SO4/H2O phase diagram.
PMID 17228897·J Phys Chem A·2007
8-other
Age at onset: an essential variable for the definition of genetic risk factors for sporadic Alzheimer's disease.
PMID 16399900·Ann N Y Acad Sci·2005
8-other
Upregulation of amyloid precursor protein isoforms containing Kunitz protease inhibitor in dementia with Lewy bodies.
PMID 15530662·Brain Res Mol Brain Res·2004
8-other
Cystathionine beta synthase as a risk factor for Alzheimer disease.
PMID 15975077·Curr Alzheimer Res·2004
8-other
Methionine synthase polymorphism is a risk factor for Alzheimer disease.
PMID 12876480·Neuroreport·2003
4-observational
The Th1/E47cs-G apolipoprotein E (APOE) promoter allele is a risk factor for Alzheimer disease of very later onset.
PMID 12095653·Neurosci Lett·2002
4-observational
Mutation analysis of the coding sequence of the MECP2 gene in infantile autism.
PMID 12384770·Hum Genet·2002
8-other
Association studies of the HOPA dodecamer duplication variant in different subtypes of autism.
PMID 11840515·Am J Med Genet·2002
8-other
Construction of a physical map of an autism susceptibility region in 7q32.3-q33.
PMID 11470513·Gene·2001
8-other
Alzheimer's disease and the cystatin C gene polymorphism: an association study.
PMID 11711204·Neurosci Lett·2001
8-other
Linear IgE-epitope mapping and comparative structural homology modeling of hazelnut and English walnut 11S globulins.
PMID 19631385·Mol Immunol·2009
4-observational
Segawa syndrome due to mutation Q89X in the GCH1 gene: a possible founder effect in Córdoba (southern Spain).
PMID 19533203·J Neurol·2009
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
- 478 S JOHNSON ST FL 7
NEW ORLEANS, LA 70112 - Phone
- (504) 412-1580
Quick Facts
- NPI
- 1891444261
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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