Giuseppe Di Fede
Giuseppe Di Fede
Istituto Neurologico "C. Besta" Milano
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A recessive mutation in the APP gene with dominant-negative effect on amyloidogenesis
G Di Fede, M Catania, M Morbin, G Rossi, S Suardi, G Mazzoleni, ...
Science 323 (5920), 1473-1477, 2009
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
R Capobianco, C Casalone, S Suardi, M Mangieri, C Miccolo, L Limido, ...
PLoS Pathog 3 (3), e31, 2007
Doxycycline in Creutzfeldt-Jakob disease: a phase 2, randomised, double-blind, placebo-controlled trial
S Ha´k, G Marcon, A Mallet, M Tettamanti, A Welaratne, G Giaccone, ...
The Lancet Neurology 13 (2), 150-158, 2014
Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype
MAB Melone, A Tessa, S Petrini, G Lus, S Sampaolo, G Di Fede, ...
Archives of neurology 61 (2), 269-272, 2004
Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP
O Bugiani, G Giaccone, G Rossi, M Mangieri, R Capobianco, M Morbin, ...
Archives of neurology 67 (8), 987-995, 2010
Neuropathology of the recessive A673V APP mutation: Alzheimer disease with distinctive features
G Giaccone, M Morbin, F Moda, M Botta, G Mazzoleni, A Uggetti, ...
Acta neuropathologica 120 (6), 803-812, 2010
The peculiar role of the A2V mutation in amyloid-β (Aβ) 1–42 molecular assembly
M Messa, L Colombo, E Del Favero, L Cant¨, T Stoilova, A Cagnotto, ...
Journal of Biological Chemistry 289 (35), 24143-24152, 2014
MM2‐Thalamic Creutzfeldt–Jakob Disease: Neuropathological, Biochemical and Transmission Studies Identify a Distinctive Prion Strain
F Moda, S Suardi, G Di Fede, A Indaco, L Limido, C Vimercati, ...
Brain Pathology 22 (5), 662-669, 2012
Specific recognition of biologically active amyloid-β oligomers by a new surface plasmon resonance-based immunoassay and an in vivo assay in Caenorhabditis elegans
M Stravalaci, A Bastone, M Beeg, A Cagnotto, L Colombo, G Di Fede, ...
Journal of Biological Chemistry 287 (33), 27796-27805, 2012
A novel Italian presenilin 2 gene mutation with prevalent behavioral phenotype
G Marcon, G Di Fede, G Giaccone, G Rossi, AR Giovagnoli, ...
Journal of Alzheimer's Disease 16 (3), 509-511, 2009
Progressive supranuclear palsy and Parkinson's disease in a family with a new mutation in the tau gene
G Rossi, E Gasparoli, C Pasquali, G Di Fede, D Testa, A Albanese, ...
Annals of neurology 55 (3), 448, 2004
Sporadic Creutzfeldt-Jakob Disease: The Extent of Microglia Activation Is Dependent on the Biochemical Type of PrPSc
G Puoti, G Giaccone, M Mangieri, L Limido, P Fociani, P Zerbi, S Suardi, ...
Journal of Neuropathology & Experimental Neurology 64 (10), 902-909, 2005
APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38
ML Moro, G Giaccone, R Lombardi, A Indaco, A Uggetti, M Morbin, ...
Acta neuropathologica 124 (6), 809-821, 2012
Good gene, bad gene: new APP variant may be both
G Di Fede, M Catania, M Morbin, G Giaccone, ML Moro, R Ghidoni, ...
Progress in neurobiology 99 (3), 281-292, 2012
Psychoneuroendocrine modulation of regulatory T lymphocyte system: in vivo and in vitro effects of the pineal immunomodulating hormone melatonin
L Vigore, G Messina, F Brivio, L Fumagalli, F Rovelli, G Di Fede, P Lissoni
in vivo 24 (5), 787-789, 2010
Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene
V Pietrini, G Puoti, L Limido, G Rossi, G Di Fede, G Giaccone, M Mangieri, ...
Neurology 61 (9), 1288-1291, 2003
The ε isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Strńussler-Scheinker disease
G Di Fede, G Giaccone, L Limido, M Mangieri, S Suardi, G Puoti, ...
Journal of Neuropathology & Experimental Neurology 66 (2), 124-130, 2007
Expression of A2V-mutated Aβ in Caenorhabditis elegans results in oligomer formation and toxicity
L Diomede, G Di Fede, M Romeo, R Bagnati, R Ghidoni, F Fiordaliso, ...
Neurobiology of disease 62, 521-532, 2014
Cancer chemotherapy-induced lymphocytosis: a revolutionary discovery in the medical oncology.
P Lissoni, L Fumagalli, F Brivio, F Rovelli, G Messina, G Di Fede, ...
Journal of biological regulators and homeostatic agents 20 (1-2), 29-35, 2006
Molecular subtypes of Alzheimer’s disease
G Di Fede, M Catania, E Maderna, R Ghidoni, L Benussi, E Tonoli, ...
Scientific reports 8 (1), 1-14, 2018
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