Pierluigi Gambetti neuropathologist
Gambetti, Pierluigi.
VIAF ID: 311772272 (Personal)
Permalink: http://viaf.org/viaf/311772272
Preferred Forms
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- 100 1 _ ‡a Gambetti, Pierluigi
- 100 1 _ ‡a Gambetti, Pierluigi
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- 100 1 _ ‡a Gambetti, Pierluigi
- 100 1 _ ‡a Gambetti, Pierluigi
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- 100 0 _ ‡a Pierluigi Gambetti ‡c neuropathologist
4xx's: Alternate Name Forms (1)
Works
Title | Sources |
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Monitoring the occurrence of emerging forms of Creutzfeldt-Jakob disease in the United States | |
Morphological and biochemical changes in rat synaptosome fractions during neonatal development | |
Morvan's syndrome: peripheral and central nervous system and cardiac involvement with antibodies to voltage-gated potassium channels | |
Myoclonic epilepsy with lafora bodies. Some ultrastructural, histochemical, and biochemical aspects. | |
Neurochemistry of dementia: establishing the links | |
Neurofibrillary changes in human brain. An immunocytochemical study with a neurofilament antiserum. | |
Neuronal and astrocytic differentiation in human neuroepithelial neoplasms. An immunohistochemical study. | |
Neuronal and microglial involvement in beta-amyloid protein deposition in Alzheimer's disease | |
The neuropathology of chromosome 17-linked dementia | |
Neuropil threads of Alzheimer's disease show a marked alteration of the normal cytoskeleton | |
Normal cellular prion protein is preferentially expressed on subpopulations of murine hemopoietic cells | |
Novel differences between two human prion strains revealed by two-dimensional gel electrophoresis. | |
Opposite roles of apolipoprotein E in normal brains and in Alzheimer's disease. | |
Oxidative impairment in scrapie-infected mice is associated with brain metals perturbations and altered antioxidant activities | |
Paired helical filaments from Alzheimer disease patients contain cytoskeletal components | |
Parkinson disease, dementia, and Alzheimer disease: clinicopathological correlations. | |
The pathophysiology of fatal familial insomnia. | |
The presence of glial fibrillary acidic protein in the human pituitary gland. | |
Prions and diseases. | |
Production of Alzheimer 4kDa beta-amyloid peptide requires the C-terminal cytosolic domain of the amyloid precursor protein | |
Progressive disruption of the circadian rhythm of melatonin in fatal familial insomnia. | |
Protease-resistant human prion protein and ferritin are cotransported across Caco-2 epithelial cells: implications for species barrier in prion uptake from the intestine. | |
Protease-sensitive prions with 144-bp insertion mutations | |
Proteasomal Degradation and N-terminal Protease Resistance of the Codon 145 Mutant Prion Protein | |
Protein synthesis in synaptosomal fractions. Ultrastructural radioautographic study | |
Proteins transported in slow components a and b of axonal transport are distributed differently in the transverse plane of the axon | |
PrPSc typing by N-terminal sequencing and mass spectrometry | |
Publisher Correction: Early preclinical detection of prions in the skin of prion-infected animals | |
Puromycin: action on neuronal mitochondria | |
Quantifying prion disease penetrance using large population control cohorts | |
Quantitative autoradiographic study of labeled RNA in rabbit optic nerve after intraocular injection of (3H)uridine | |
R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia | |
Reorganization of axoplasmic organelles following beta, beta'-iminodipropionitrile administration | |
Ribonucleic acid and axonal transport. Study on optic nerve regeneration in the red fish | |
RNA and axonal flow. Biochemical and autoradiographic study in the rabbit optic system. | |
Role of amyloid precursor protein (APP): study with antisense transfection of human neuroblastoma cells | |
The role of glycophosphatidylinositol anchor in the amplification of the scrapie isoform of prion protein in vitro | |
Role of prion protein glycosylation in replication of human prions by protein misfolding cyclic amplification | |
Selective presence of ubiquitin in intracellular inclusions | |
The significance of cytoplasmic inclusions in late infantile and juvenile amaurotic idiocy. An ultrastructural study. | |
Sleep-wake cycle abnormalities in fatal familial insomnia. Evidence of the role of the thalamus in sleep regulation. | |
Soluble amyloid-beta in the brain: the scarlet pimpernel | |
Soluble amyloid beta-protein is a marker of Alzheimer amyloid in brain but not in cerebrospinal fluid. | |
Soluble amyloid beta-protein is increased in frontotemporal dementia with tau gene mutations. | |
Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy | |
Sporadic and familial CJD: classification and characterisation. | |
Sporadic fatal insomnia: a case study. | |
Status spongiosus of rat central nervous system induced by actinomycin D | |
Structural basis of gamma-diketone neurotoxicity: non-neurotoxicity of 3,3-dimethyl-2,5-hexanedione, a gamma-diketone incapable of pyrrole formation | |
Subcellular localization of amyloid precursor protein in senile plaques of Alzheimer's disease | |
Synapses and malnutrition: Quantitative ultrastructural study of rat cerebral cortex | |
Targeting prion amyloid deposits in vivo. | |
Tau gene mutation in familial progressive subcortical gliosis. | |
Thermodynamic Stabilization of the Folded Domain of Prion Protein Inhibits Prion Infection in Vivo | |
Toxic effects of intracerebral PrP antibody administration during the course of BSE infection in mice | |
Transthyretin amyloidosis: a new mutation associated with dementia | |
Treatable neurological disorders misdiagnosed as Creutzfeldt-Jakob disease | |
Tribute to Robert Terry | |
Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease. | |
Typing prion isoforms. | |
Ubiquitin and heat shock proteins in cultured nervous tissue after different stress conditions | |
Ubiquitin in motor neuron disease: study at the light and electron microscope | |
Ubiquitin is associated with abnormal cytoplasmic filaments characteristic of neurodegenerative diseases | |
Ubiquitin is present on the cytokeratin intermediate filaments and Mallory bodies of hepatocytes | |
Ubiquitinated filamentous inclusions in spinal cord of patients with motor neuron disease | |
Ultrastructural autoradiographic detection of intracellular immunoglobulins with iodinated Fab fragments of antibody. The combined use of ultrastructural autoradiography and peroxidase cytochemistry for the detection of two antigens (double labeling | |
Ultrastructural localization of beta-amyloid, tau, and ubiquitin epitopes in extracellular neurofibrillary tangles | |
Variably protease-sensitive prionopathy: a novel disease of the prion protein | |
Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study | |
Washington statewide pathology surveillance for prion disease | |
The widespread alteration of neurites in Alzheimer's disease may be unrelated to amyloid deposition |