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MARY MANGIERI, MD
Student in an Organized Health Care Education/Training Program
NPI: 1740985142Individual
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 (15)
Mutant prion protein expression causes motor and memory deficits and abnormal sleep patterns in a transgenic mouse model.
PMID 19038218·Neuron·2008
7-preclinical
Tauopathy in human and experimental variant Creutzfeldt-Jakob disease.
PMID 17560687·Neurobiol Aging·2008
7-preclinical
The efficacy of tetracyclines in peripheral and intracerebral prion infection.
PMID 18365024·PLoS One·2008
7-preclinical
Atypical tauopathy with massive involvement of the white matter.
PMID 18208485·Neuropathol Appl Neurobiol·2008
8-other
A new function of microtubule-associated protein tau: involvement in chromosome stability.
PMID 18583940·Cell Cycle·2008
8-other
A novel phenotype of sporadic Creutzfeldt-Jakob disease.
PMID 18024694·J Neurol Neurosurg Psychiatry·2007
5-case
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
PMID 17352534·PLoS Pathog·2007
7-preclinical
The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease.
PMID 17278997·J Neuropathol Exp Neurol·2007
8-other
Pathologic prion protein is specifically recognized in situ by a novel PrP conformational antibody.
PMID 16876426·Neurobiol Dis·2006
8-other
Defective tumor necrosis factor-alpha-dependent control of astrocyte glutamate release in a transgenic mouse model of Alzheimer disease.
PMID 16253995·J Biol Chem·2005
7-preclinical
Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPSc.
PMID 16215462·J Neuropathol Exp Neurol·2005
8-other
A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene.
PMID 15365148·Neurology·2004
8-other
Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene.
PMID 14610142·Neurology·2003
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 975 E 3RD ST # 112
CHATTANOOGA, TN 37403 - Phone
- (423) 778-7817
Quick Facts
- NPI
- 1740985142
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 15
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