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Neurology
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August 1, 2022
α-Synuclein Seed Amplification Assays for Diagnosing Synucleinopathies: The Way Forward
Giovanni Bellomo, Chiara Maria Giulia De Luca, Federico Paolini Paoletti, et al.
European Journal of Histochemistry : EJH
|
October 18, 2021
Sporadic Creutzfeldt-Jakob disease: Real-Time Quaking Induced Conversion (RT-QuIC) assay represents a major diagnostic advance
Federico Angelo Cazzaniga, Edoardo Bistaffa, Chiara Maria Giulia De Luca, et al.
Progress in Molecular Biology and Translational Science
|
September 22, 2020
Cell-free amplification of prions: Where do we stand?
Federico Angelo Cazzaniga, Chiara Maria Giulia De Luca, Edoardo Bistaffa, et al.
International Journal of Molecular Sciences
|
January 24, 2019
Investigating the Molecular Basis of the Aggregation Propensity of the Pathological D76N Mutant of Beta-2 Microglobulin: Role of the Denatured State
Lorenzo Visconti, Francesca Malagrinò, Luca Broggini, et al.
Biomedicines
|
August 6, 2021
Animal Models of Autosomal Recessive Parkinsonism
Guendalina Bastioli, Maria Regoni, Federico Cazzaniga, et al.
Molecular Neurobiology
|
August 4, 2018
Synthetic Prion Selection and Adaptation
Edoardo Bistaffa, Fabio Moda, Tommaso Virgilio, et al.
Molecular Neurobiology
|
May 2, 2019
Prion Efficiently Replicates in α-Synuclein Knockout Mice
Edoardo Bistaffa, Martina Rossi, Chiara Maria Giulia De Luca, et al.
Prion
|
April 21, 2018
Effects of peptidyl-prolyl isomerase 1 depletion in animal models of prion diseases
Giuseppe Legname, Tommaso Virgilio, Edoardo Bistaffa, et al.
Plos Pathogens
|
October 16, 2025
Substitution of histidine 95 by tyrosine in the prion protein causes spontaneous neurodegeneration in transgenic mice
Juan-María Torres, Alba Marín-Moreno, Juan-Carlos Espinosa, et al.
Brain Sciences
|
November 24, 2022
Approaching the Gut and Nasal Microbiota in Parkinson's Disease in the Era of the Seed Amplification Assays
Alessandra Consonni, Martina Miglietti, Chiara Maria Giulia De Luca, et al.
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Search research articles
Search
Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 3
Neurology
|
August 1, 2022
α-Synuclein Seed Amplification Assays for Diagnosing Synucleinopathies: The Way Forward
Giovanni Bellomo, Chiara Maria Giulia De Luca, Federico Paolini Paoletti, et al.
European Journal of Histochemistry : EJH
|
October 18, 2021
Sporadic Creutzfeldt-Jakob disease: Real-Time Quaking Induced Conversion (RT-QuIC) assay represents a major diagnostic advance
Federico Angelo Cazzaniga, Edoardo Bistaffa, Chiara Maria Giulia De Luca, et al.
Progress in Molecular Biology and Translational Science
|
September 22, 2020
Cell-free amplification of prions: Where do we stand?
Federico Angelo Cazzaniga, Chiara Maria Giulia De Luca, Edoardo Bistaffa, et al.
International Journal of Molecular Sciences
|
January 24, 2019
Investigating the Molecular Basis of the Aggregation Propensity of the Pathological D76N Mutant of Beta-2 Microglobulin: Role of the Denatured State
Lorenzo Visconti, Francesca Malagrinò, Luca Broggini, et al.
Biomedicines
|
August 6, 2021
Animal Models of Autosomal Recessive Parkinsonism
Guendalina Bastioli, Maria Regoni, Federico Cazzaniga, et al.
Molecular Neurobiology
|
August 4, 2018
Synthetic Prion Selection and Adaptation
Edoardo Bistaffa, Fabio Moda, Tommaso Virgilio, et al.
Molecular Neurobiology
|
May 2, 2019
Prion Efficiently Replicates in α-Synuclein Knockout Mice
Edoardo Bistaffa, Martina Rossi, Chiara Maria Giulia De Luca, et al.
Prion
|
April 21, 2018
Effects of peptidyl-prolyl isomerase 1 depletion in animal models of prion diseases
Giuseppe Legname, Tommaso Virgilio, Edoardo Bistaffa, et al.
Plos Pathogens
|
October 16, 2025
Substitution of histidine 95 by tyrosine in the prion protein causes spontaneous neurodegeneration in transgenic mice
Juan-María Torres, Alba Marín-Moreno, Juan-Carlos Espinosa, et al.
Brain Sciences
|
November 24, 2022
Approaching the Gut and Nasal Microbiota in Parkinson's Disease in the Era of the Seed Amplification Assays
Alessandra Consonni, Martina Miglietti, Chiara Maria Giulia De Luca, et al.
Page
of 3