Physician
Pathology
Dr. Bernardino Ghetti, MD
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Bernardino Ghetti works in the field of Pathology. He went to Albert Einstein College of Medicine at Jacobi Medical Center. Bernardino Ghetti is also published. He has 30 publications published. The lastest publication: "Quantitative Amyloid Imaging in Autosomal Dominant Alzheimer's Disease: Results from the DIAN Study Group.'
Publications
- Fulminant corticobasal degeneration: Agrypnia excitata in corticobasal syndrome.
- Early behavioural changes in familial Alzheimer's disease in the Dominantly Inherited Alzheimer Network.
- Protective variant for hippocampal atrophy identified by whole exome sequencing.
- Neuronal NLRP1 inflammasome activation of Caspase-1 coordinately regulates inflammatory interleukin-1-beta production and axonal degeneration-associated Caspase-6 acti...
- Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging.
- The Tau Tubulin Kinases TTBK1/2 Promote Accumulation of Pathological TDP-43.
- Rarity of the Alzheimer Disease-Protective APP A673T Variant in the United States.
- Effects of Multiple Genetic Loci on Age at Onset in Late-Onset Alzheimer Disease: A Genome-Wide Association Study.
- Genetic heterogeneity in Alzheimer disease and implications for treatment strategies.
- Functional connectivity in autosomal dominant and late-onset Alzheimer disease.
- Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias.
- Visuoperception test predicts pathologic diagnosis of Alzheimer disease in corticobasal syndrome.
- Symptom onset in autosomal dominant Alzheimer disease: A systematic review and meta-analysis.
- Rapid-onset dystonia-parkinsonism associated with the I758S mutation of the ATP1A3 gene: a neuropathologic and neuroanatomical study of four siblings.
- Longitudinal Change in CSF Biomarkers in Autosomal-Dominant Alzheimer's Disease.
- TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions.
- Regional variability of imaging biomarkers in autosomal dominant Alzheimer's disease.
- Preclinical trials in autosomal dominant AD: Implementation of the DIAN-TU trial.
- The pattern of atrophy in familial Alzheimer disease: Volumetric MRI results from the DIAN study.
- Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics.
- Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairment.
- Increased Tau Phosphorylation and Tau Truncation, and Decreased Synaptophysin Levels in Mutant BRI(2)/Tau Transgenic Mice.
- Phenotypic variability in three families with valosin-containing protein mutation.
- Generation of a novel murine model of Aβ deposition based on the expression of human wild-type amyloid precursor protein gene.
- The Psen1-L166P-knock-in mutation leads to amyloid deposition in human wild-type amyloid precursor protein YAC transgenic mice.
- Cerebral hypometabolism and grey matter density in MAPT intron 10 +3 mutation carriers.
- Systemic and cerebral iron homeostasis in ferritin knock-out mice.
- Influence of genetic variation on plasma protein levels in older adults using a multi-analyte panel.
- Quantitative Amyloid Imaging in Autosomal Dominant Alzheimer's Disease: Results from the DIAN Study Group.
Schools
Universita Di Pisa Facolta Di Medicina E Chirurgia
Santa Chiara Hospital
Einstein College Med
Doctors Specialties
- Neuropathology
- Pathology
Accepted Insurances
Education
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Albert Einstein College of Medicine at Jacobi Medical Center -
University of Pisa Faculty of Medicine
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