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MARYLOU HEAD, D.M.D.
D.M.D.
General Practice Dentistry
NPI: 1780799908Individual
Specialties, Licenses & Credentials
General Practice DentistryPrimary
Dentist — General Practice
Code: 1223G0001X
4853(KY)
Dentist
Dentist
Code: 122300000X
4853(KY)
Research & Publications (20)
Variant Creutzfeldt-Jakob disease in France and the United Kingdom: Evidence for the same agent strain.
PMID 19334063·Ann Neurol·2009
4-observational
An antibody to the aggregated synthetic prion protein peptide (PrP106-126) selectively recognizes disease-associated prion protein (PrP) from human brain specimens.
PMID 18507665·Brain Pathol·2009
7-preclinical
Inter-laboratory assessment of PrPSc typing in creutzfeldt-jakob disease: a Western blot study within the NeuroPrion Consortium.
PMID 18624793·Brain Pathol·2009
4-observational
Organ procurement and transplantation network/united network for organ sharing histocompatibility committee collaborative study to evaluate prediction of crossmatch results in highly sensitized patients.
PMID 19307794·Transplantation·2009
8-other
Variation in bone mineral density by anatomical site in patients with proximal humeral fractures.
PMID 19483231·J Bone Joint Surg Br·2009
8-other
A case of protease sensitive prionopathy in a patient in the UK.
PMID 19671081·Neuropathol Appl Neurobiol·2009
5-case
Transmissions of variant Creutzfeldt-Jakob disease from brain and lymphoreticular tissue show uniform and conserved bovine spongiform encephalopathy-related phenotypic properties on primary and secondary passage in wild-type mice.
PMID 19656962·J Gen Virol·2009
7-preclinical
Pathological investigation of the first blood donor and recipient pair linked by transfusion-associated variant Creutzfeldt-Jakob disease transmission.
PMID 19490428·Neuropathol Appl Neurobiol·2009
8-other
Further characterisation of the prion protein molecular types detectable in the NIBSC Creutzfeldt-Jakob disease brain reference materials.
PMID 19264507·Biologicals·2009
8-other
Familial prion disease with a novel serine to isoleucine mutation at codon 132 of prion protein gene (PRNP).
PMID 19187063·Neuropathol Appl Neurobiol·2009
5-case
Production and characterization of a panel of monoclonal antibodies against native human cellular prion protein.
PMID 19132894·Hybridoma (Larchmt)·2009
7-preclinical
Human platelets as a substrate source for the in vitro amplification of the abnormal prion protein (PrP) associated with variant Creutzfeldt-Jakob disease.
PMID 18980616·Transfusion·2009
8-other
Body size differences do not arise from divergent mate preferences in a species pair of threespine stickleback.
PMID 19474072·Biol Lett·2009
7-preclinical
Blind docking of pharmaceutically relevant compounds using RosettaLigand.
PMID 19554568·Protein Sci·2009
8-other
Panencephalopathic Creutzfeldt-Jakob disease in the Netherlands and the UK: clinical and pathological characteristics of nine patients.
PMID 19473294·Neuropathol Appl Neurobiol·2009
8-other
Design and synthesis of orally bioavailable serum and glucocorticoid-regulated kinase 1 (SGK1) inhibitors.
PMID 19497745·Bioorg Med Chem Lett·2009
7-preclinical
No major change in vCJD agent strain after secondary transmission via blood transfusion.
PMID 18682737·PLoS One·2008
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3225 SUMMIT SQUARE PL, SUITE 150
LEXINGTON, KY 40509 - Phone
- (859) 269-5386
Quick Facts
- NPI
- 1780799908
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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