Bernardino F. Ghetti neuropathologist
Ghetti, Bernardino
VIAF ID: 54044905 (Personal)
Permalink: http://viaf.org/viaf/54044905
Preferred Forms
- 100 0 _ ‡a Bernardino F. Ghetti ‡c neuropathologist
- 100 1 0 ‡a Ghetti, Bernardino
-
4xx's: Alternate Name Forms (1)
Works
Title | Sources |
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[(11)C]PiB PET in Gerstmann-Sträussler-Scheinker disease | |
Increase in the relative expression of tau with four microtubule binding repeat regions in frontotemporal lobar degeneration and progressive supranuclear palsy brains | |
Influence of genetic variation on plasma protein levels in older adults using a multi-analyte panel | |
LATE to the PART-y | |
Living Neurons with Tau Filaments Aberrantly Expose Phosphatidylserine and Are Phagocytosed by Microglia | |
Longitudinal characterization of two siblings with frontotemporal dementia and parkinsonism linked to chromosome 17 associated with the S305N tau mutation. | |
Million-fold sensitivity enhancement in proteopathic seed amplification assays for biospecimens by Hofmeister ion comparisons | |
Modeling familial British and Danish dementia | |
MRI characteristics and scoring in HDLS due to CSF1R gene mutations | |
Mutant presenilin 1 increases the expression and activity of BACE1 | |
Mutations in the tau gene (MAPT) in FTDP-17: the family with Multiple System Tauopathy with Presenile Dementia (MSTD). | |
Neocortical variation of Abeta load in fully expressed, pure Alzheimer's disease. | |
Neurodegeneration-Associated Proteins in Human Olfactory Neurons Collected by Nasal Brushing | |
Neurodegeneration caused by proteins with an aberrant carboxyl-terminus | |
Neuropathologic assessment of participants in two multi-center longitudinal observational studies: the Alzheimer Disease Neuroimaging Initiative (ADNI) and the Dominantly Inherited Alzheimer Network (DIAN). | |
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations | |
Novel late-onset Alzheimer disease loci variants associate with brain gene expression | |
A novel mutation (G217D) in the Presenilin 1 gene ( PSEN1) in a Japanese family: presenile dementia and parkinsonism are associated with cotton wool plaques in the cortex and striatum | |
Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type | |
Novel tau filament fold in chronic traumatic encephalopathy encloses hydrophobic molecules | |
Novel tau filament fold in corticobasal degeneration | |
The novel Tau mutation G335S: clinical, neuropathological and molecular characterization. | |
P301L tauopathy: confocal immunofluorescence study of perinuclear aggregation of the mutated protein. | |
P4-242 Oxidative damage in ferritin-induced neurodegeneration | |
PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease | |
Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations | |
Pathologic prion protein is specifically recognized in situ by a novel PrP conformational antibody. | |
Pathological changes in dopaminergic nerve cells of the substantia nigra and olfactory bulb in mice transgenic for truncated human alpha-synuclein(1-120): implications for Lewy body disorders. | |
The pattern of atrophy in familial Alzheimer disease: volumetric MRI results from the DIAN study | |
Performance on MMSE sub-items and education level in presenilin-1 mutation carriers without dementia | |
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative. | |
The phosphatase calcineurin regulates pathological TDP-43 phosphorylation. | |
Preferential degradation of cognitive networks differentiates Alzheimer's disease from ageing. | |
Presence of reactive microglia and neuroinflammatory mediators in a case of frontotemporal dementia with P301S mutation | |
Presenilin-1 280Glu-->Ala mutation alters C-terminal APP processing yielding longer abeta peptides: implications for Alzheimer's disease | |
Presenilin-1 mutations of leucine 166 equally affect the generation of the Notch and APP intracellular domains independent of their effect on Abeta 42 production | |
Protective variant for hippocampal atrophy identified by whole exome sequencing | |
The Psen1-L166P-knock-in mutation leads to amyloid deposition in human wild-type amyloid precursor protein YAC transgenic mice. | |
Quantitative Amyloid Imaging in Autosomal Dominant Alzheimer's Disease: Results from the DIAN Study Group | |
Rapid-onset dystonia-parkinsonism associated with the I758S mutation of the ATP1A3 gene: a neuropathologic and neuroanatomical study of four siblings | |
Rapidly progressive primary progressive aphasia and parkinsonism with novel GRN mutation. | |
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease | |
Rarity of the Alzheimer disease-protective APP A673T variant in the United States | |
Redox metals and oxidative abnormalities in human prion diseases | |
Relationships between big-five personality factors and Alzheimer's disease pathology in autosomal dominant Alzheimer's disease | |
Ricerche storiche, 1906: | |
Screening for C9ORF72 repeat expansion in FTLD. | |
Sequence of Alzheimer disease biomarker changes in cognitively normal adults: A cross-sectional study | |
Serum neurofilament dynamics predicts neurodegeneration and clinical progression in presymptomatic Alzheimer’s disease | |
Serum neurofilament light chain levels are associated with white matter integrity in autosomal dominant Alzheimer's disease | |
Silver staining (Campbell-Switzer) of neuronal α-synuclein assemblies induced by multiple system atrophy and Parkinson's disease brain extracts in transgenic mice | |
Single-subject grey matter network trajectories over the disease course of autosomal dominant Alzheimer's disease | |
A single ultrasensitive assay for detection and discrimination of tau aggregates of Alzheimer and Pick diseases | |
SNARE protein redistribution and synaptic failure in a transgenic mouse model of Parkinson's disease | |
Soluble amyloid beta-protein is increased in frontotemporal dementia with tau gene mutations. | |
Structure-based classification of tauopathies | |
Structure-based inhibitors halt prion-like seeding by Alzheimer's disease-and tauopathy-derived brain tissue samples | |
Structures of filaments from Pick's disease reveal a novel tau protein fold | |
Structures of α-synuclein filaments from multiple system atrophy | |
Subjects harboring presenilin familial Alzheimer's disease mutations exhibit diverse white matter biochemistry alterations | |
Symptom onset in autosomal dominant Alzheimer disease: a systematic review and meta-analysis | |
Systemic and cerebral iron homeostasis in ferritin knock-out mice | |
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea. | |
Tau filaments from multiple cases of sporadic and inherited Alzheimer's disease adopt a common fold | |
The tau tubulin kinases TTBK1/2 promote accumulation of pathological TDP-43 | |
The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family | |
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions | |
Ubiquitination of alpha-synuclein in Lewy bodies is a pathological event not associated with impairment of proteasome function | |
Ultrasensitive and selective detection of 3-repeat tau seeding activity in Pick disease brain and cerebrospinal fluid. | |
Visuoperception test predicts pathologic diagnosis of Alzheimer disease in corticobasal syndrome | |
White matter hyperintensities are a core feature of Alzheimer's disease: Evidence from the dominantly inherited Alzheimer network | |
White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration | |
α-Synuclein filaments from transgenic mouse and human synucleinopathy-containing brains are major seed-competent species | |
α-Synuclein RT-QuIC assay in cerebrospinal fluid of patients with dementia with Lewy bodies |