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Giuseppe Di Fede

Showing results (71-80 of 84) with videos related to

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Archives of Neurology|August 11, 2010
Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APPOrso Bugiani, Giorgio Giaccone, Giacomina Rossi, et al.
Acta Neuropathologica Communications|January 5, 2019
Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein geneGiuseppe Di Fede, Marcella Catania, Cristiana Atzori, et al.
Plos Pathogens|March 14, 2007
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?Raffaella Capobianco, Cristina Casalone, Silvia Suardi, et al.
Neurology|September 16, 2024
CSF and Plasma Biomarkers in Patients With Iatrogenic Cerebral Amyloid AngiopathyGiuliana Pollaci, Antonella Potenza, Gemma Gorla, et al.
Science (New York, N.Y.)|March 17, 2009
A recessive mutation in the APP gene with dominant-negative effect on amyloidogenesisGiuseppe Di Fede, Marcella Catania, Michela Morbin, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 16, 2025
Detection of TDP-43 seeds in CSF of presymptomatic and symptomatic genetic FTD/ALSIlaria Linda Dellarole, Vittoria Aprea, Marcella Catania, et al.
Journal of Alzheimer'S Disease : JAD|February 23, 2016
Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus ProtocolMartina Bocchetta, Anna Mega, Livia Bernardi, et al.
Frontiers in Aging Neuroscience|April 11, 2022
PMCA-Based Detection of Prions in the Olfactory Mucosa of Patients With Sporadic Creutzfeldt-Jakob DiseaseFederico Angelo Cazzaniga, Edoardo Bistaffa, Chiara Maria Giulia De Luca, et al.
Frontiers in Aging Neuroscience|March 16, 2023
Corrigendum: PMCA-based detection of prions in the olfactory mucosa of patients with sporadic Creutzfeldt-Jakob diseaseFederico Angelo Cazzaniga, Edoardo Bistaffa, Chiara Maria Giulia De Luca, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 14, 2020
Discovering the Italian phenotype of cerebral amyloid angiopathy (CAA): the SENECA projectAnna Bersano, Emma Scelzo, Leonardo Pantoni, et al.
Pageof 9

Showing results (71-80 of 84) with videos related to

Sort By:
Pageof 9
Archives of Neurology|August 11, 2010
Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APPOrso Bugiani, Giorgio Giaccone, Giacomina Rossi, et al.
Acta Neuropathologica Communications|January 5, 2019
Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein geneGiuseppe Di Fede, Marcella Catania, Cristiana Atzori, et al.
Plos Pathogens|March 14, 2007
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?Raffaella Capobianco, Cristina Casalone, Silvia Suardi, et al.
Neurology|September 16, 2024
CSF and Plasma Biomarkers in Patients With Iatrogenic Cerebral Amyloid AngiopathyGiuliana Pollaci, Antonella Potenza, Gemma Gorla, et al.
Science (New York, N.Y.)|March 17, 2009
A recessive mutation in the APP gene with dominant-negative effect on amyloidogenesisGiuseppe Di Fede, Marcella Catania, Michela Morbin, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 16, 2025
Detection of TDP-43 seeds in CSF of presymptomatic and symptomatic genetic FTD/ALSIlaria Linda Dellarole, Vittoria Aprea, Marcella Catania, et al.
Journal of Alzheimer'S Disease : JAD|February 23, 2016
Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus ProtocolMartina Bocchetta, Anna Mega, Livia Bernardi, et al.
Frontiers in Aging Neuroscience|April 11, 2022
PMCA-Based Detection of Prions in the Olfactory Mucosa of Patients With Sporadic Creutzfeldt-Jakob DiseaseFederico Angelo Cazzaniga, Edoardo Bistaffa, Chiara Maria Giulia De Luca, et al.
Frontiers in Aging Neuroscience|March 16, 2023
Corrigendum: PMCA-based detection of prions in the olfactory mucosa of patients with sporadic Creutzfeldt-Jakob diseaseFederico Angelo Cazzaniga, Edoardo Bistaffa, Chiara Maria Giulia De Luca, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 14, 2020
Discovering the Italian phenotype of cerebral amyloid angiopathy (CAA): the SENECA projectAnna Bersano, Emma Scelzo, Leonardo Pantoni, et al.
Pageof 9