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BERNARDINO GHETTI, M.D.
M.D.
Clinical Pathology/Laboratory Medicine Physician
NPI: 1821040452Individual
Specialties, Licenses & Credentials
Clinical Pathology/Laboratory Medicine PhysicianPrimary
Pathology — Clinical Pathology/Laboratory Medicine
Code: 207ZP0105X
01027412A(IN)
Research & Publications (20)
In vivo and postmortem clinicoanatomical correlations in frontotemporal dementia and parkinsonism linked to chromosome 17.
PMID 18322394·Neurodegener Dis·2008
4-observational
Neurodegeneration and hereditary dementias: 40 years of learning.
PMID 17004363·J Alzheimers Dis·2006
6-review
Progress in hereditary tauopathies: a mutation in the Tau gene (G389R) causes a Pick disease-like syndrome.
PMID 11193177·Ann N Y Acad Sci·2000
8-other
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.
PMID 19609911·Mov Disord·2009
8-other
Failure to detect the presence of prions in the uterine and gestational tissues from a Gravida with Creutzfeldt-Jakob disease.
PMID 19349373·Am J Pathol·2009
5-case
Regional differences in the vulnerability of substantia nigra dopaminergic neurons in weaver mice.
PMID 19593334·Acta Neurobiol Exp (Wars)·2009
7-preclinical
Cerebral amyloid angiopathy and parenchymal amyloid deposition in transgenic mice expressing the Danish mutant form of human BRI2.
PMID 18410407·Brain Pathol·2009
7-preclinical
Abnormal iron metabolism and oxidative stress in mice expressing a mutant form of the ferritin light polypeptide gene.
PMID 19519778·J Neurochem·2009
7-preclinical
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations.
PMID 19015862·Acta Neuropathol·2009
8-other
Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498-499InsTC).
PMID 19514068·Mov Disord·2009
5-case
Mutant presenilin 1 increases the expression and activity of BACE1.
PMID 19196715·J Biol Chem·2009
7-preclinical
Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease.
PMID 18753138·J Biol Chem·2008
8-other
Detection of filamentous tau inclusions by the fluorescent Congo red derivative FSB [(trans,trans)-1-fluoro-2,5-bis(3-hydroxycarbonyl-4-hydroxy)styrylbenzene].
PMID 18291106·FEBS Lett·2008
7-preclinical
Expression of a mutant form of the ferritin light chain gene induces neurodegeneration and iron overload in transgenic mice.
PMID 18171923·J Neurosci·2008
7-preclinical
Analysis of tau phosphorylation and truncation in a mouse model of human tauopathy.
PMID 18079436·Am J Pathol·2008
7-preclinical
Histopathological and molecular heterogeneity among individuals with dementia associated with Presenilin mutations.
PMID 19021905·Mol Neurodegener·2008
8-other
Aggregated, wild-type prion protein causes neurological dysfunction and synaptic abnormalities.
PMID 19052217·J Neurosci·2008
7-preclinical
White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration.
PMID 18800011·J Neuropathol Exp Neurol·2008
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
- 635 BARNHILL DR, A128
INDIANAPOLIS, IN 46202 - Phone
- (317) 274-4806
Quick Facts
- NPI
- 1821040452
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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