Researcher
Giuseppe di Fede
Fondazione IRCCS Istituto Neurologico Carlo Besta
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111 papers found
Papers authored by Giuseppe di Fede
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Marcella Catania ,
Dominic M. Walsh,
Andrea Demarchi,
Annemieke Rozemuller,
Nenad Bogdanovic,
Orso Bugiani,
Bernardino Ghetti
and 1 other authors
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Marcella Catania ,
Dominic M. Walsh,
Andrea Demarchi,
Annemieke Rozemuller,
Nenad Bogdanovic,
Orso Bugiani,
Bernardino Ghetti
and 1 other authors
APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38
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Fabrizio Tagliavini,
Laura Cantù,
Elena Del Favero,
Michele Mazzanti ,
Roberto Chiesa,
Mario Salmona,
Luisa Diomede,
Marco Gobbi
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Marcella Catania ,
Michela Morbin,
Giorgio Giaccone,
Maria Luisa Moro,
Roberta Ghidoni ,
Laura Colombo,
Massimo Messa,
Alfredo Cagnotto,
Margherita Romeo ,
Matteo Stravalaci,
Luisa Diomede,
Marco Gobbi,
Mario Salmona,
Fabrizio Tagliavini
Good gene, bad gene: New APP variant may be both
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Silvia Suardi,
Giuseppe Di Fede ,
Antonio Indaco,
Lucia Limido,
Chiara Vimercati,
Margherita Ruggerone,
Ilaria Campagnani,
Jan Langeveld,
Alessandro Terruzzi,
Antonio Brambilla,
Pietro Zerbi,
Paolo Fociani,
Matthew T. Bishop,
Robert G. Will
and 3 other authors
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Carolina Foglia,
Elena Piccoli,
Giuseppe Piscosquito,
Dario Saracino,
Fabrizio Tagliavini,
Roberto Cotrufo
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Vidmer Scaioli,
Ferruccio Panzica,
Elisa Visani,
Giuseppe Di Fede ,
Giorgio Giaccone,
Alberto Bizzi,
Orso Bugiani,
Guiliano Avanzini,
Fabrizio Tagliavini,
Silvana Franceschetti
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Mario Botta,
Giulia Mazzoleni,
Andrea Uggetti,
Marcella Catania ,
Maria Luisa Moro,
Veronica Redaelli,
Alberto Spagnoli,
Roberta Simona Rossi,
Mario Salmona,
Giuseppe Di Fede ,
Fabrizio Tagliavini
Neuropathology of the recessive A673V APP mutation: Alzheimer disease with distinctive features
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Gianfranco Puoti,
Francesco Carella,
Andrea Salmaggi
and 5 other authors
Hereditary Cerebral Hemorrhage With Amyloidosis Associated With the E693K Mutation of APP
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Silvia Suardi,
Rosaria Strammiello,
Piero Parchi,
Fabrizio Tagliavini,
Luigi Murri
Creutzfeldt–Jakob disease with E200K PRNP mutation: a case report and revision of the literature
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Marcella Catania ,
Michela Morbin,
Giacomina Rossi,
Silvia Suardi,
Giulia Mazzoleni,
Marco Merlin,
Anna Rita Giovagnoli,
Sara Prioni,
Alessandra Erbetta,
Chiara Falcone,
Marco Gobbi,
Laura Colombo,
Antonio Bastone,
Marten Beeg
and 8 other authors
A Recessive Mutation in the APP Gene with Dominant-Negative Effect on Amyloidogenesis
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A. Leonardi,
C. Coppola,
S. Formisano,
F. Tagliavini,
R. Cotrufo,
G. Puoti
A novel insertional mutation in the prion protein gene: Clinical and bio-molecular findings
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Anna Aresi,
Fabiola Reati,
Giacomina Rossi,
Fabrizio Tagliavini
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Marcella Catania ,
Giuseppe Di Fede ,
Michela Mangieri,
Giorgio Giaccone,
Danilo Croci,
Fabrizio Tagliavini
A new function of microtubule-associated protein tau: Involvement in chromosome stability
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