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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
February 15, 2022
Correction to: The cognitive phenotypes of Creutzfeldt‑Jakob disease: comparison with secondary metabolic encephalopathy
Anna Rita Giovagnoli, Giuseppe Di Fede, Giacomina Rossi, et al.
Molecular Neurobiology
|
February 3, 2019
Prions Strongly Reduce NMDA Receptor S-Nitrosylation Levels at Pre-symptomatic and Terminal Stages of Prion Diseases
Elisa Meneghetti, Lisa Gasperini, Tommaso Virgilio, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
January 28, 2022
The cognitive phenotypes of Creutzfeldt-Jakob disease: comparison with secondary metabolic encephalopathy
Anna Rita Giovagnoli, Giuseppe Di Fede, Giacomina Rossi, et al.
Cell Reports
|
May 19, 2015
Grass plants bind, retain, uptake, and transport infectious prions
Sandra Pritzkow, Rodrigo Morales, Fabio Moda, et al.
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.
Science Translational Medicine
|
December 23, 2016
Detection of prions in blood from patients with variant Creutzfeldt-Jakob disease
Luis Concha-Marambio, Sandra Pritzkow, Fabio Moda, et al.
Journal of Neurochemistry
|
May 13, 2020
The uptake of tau amyloid fibrils is facilitated by the cellular prion protein and hampers prion propagation in cultured cells
Elena De Cecco, Luigi Celauro, Silvia Vanni, et al.
Sub-Cellular Biochemistry
|
September 26, 2025
Seed Amplification Assays as Powerful Tools for Detecting Peripheral Biomarkers in Prion-Like Diseases
Ilaria Linda Dellarole, Annalisa Lombardo, Arianna Ciullini, 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.
Frontiers in Neurology
|
September 21, 2018
Sporadic MM-1 Type Creutzfeldt-Jakob Disease With Hemiballic Presentation and No Cognitive Impairment Until Death: How New NCJDRSU Diagnostic Criteria May Allow Early Diagnosis
Lorenzo Saraceno, Vito A G Ricigliano, Michele Cavalli, et al.
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Showing results (11-20 of 101) with videos related to
Sort By:
Page
of 11
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
February 15, 2022
Correction to: The cognitive phenotypes of Creutzfeldt‑Jakob disease: comparison with secondary metabolic encephalopathy
Anna Rita Giovagnoli, Giuseppe Di Fede, Giacomina Rossi, et al.
Molecular Neurobiology
|
February 3, 2019
Prions Strongly Reduce NMDA Receptor S-Nitrosylation Levels at Pre-symptomatic and Terminal Stages of Prion Diseases
Elisa Meneghetti, Lisa Gasperini, Tommaso Virgilio, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
January 28, 2022
The cognitive phenotypes of Creutzfeldt-Jakob disease: comparison with secondary metabolic encephalopathy
Anna Rita Giovagnoli, Giuseppe Di Fede, Giacomina Rossi, et al.
Cell Reports
|
May 19, 2015
Grass plants bind, retain, uptake, and transport infectious prions
Sandra Pritzkow, Rodrigo Morales, Fabio Moda, et al.
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.
Science Translational Medicine
|
December 23, 2016
Detection of prions in blood from patients with variant Creutzfeldt-Jakob disease
Luis Concha-Marambio, Sandra Pritzkow, Fabio Moda, et al.
Journal of Neurochemistry
|
May 13, 2020
The uptake of tau amyloid fibrils is facilitated by the cellular prion protein and hampers prion propagation in cultured cells
Elena De Cecco, Luigi Celauro, Silvia Vanni, et al.
Sub-Cellular Biochemistry
|
September 26, 2025
Seed Amplification Assays as Powerful Tools for Detecting Peripheral Biomarkers in Prion-Like Diseases
Ilaria Linda Dellarole, Annalisa Lombardo, Arianna Ciullini, 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.
Frontiers in Neurology
|
September 21, 2018
Sporadic MM-1 Type Creutzfeldt-Jakob Disease With Hemiballic Presentation and No Cognitive Impairment Until Death: How New NCJDRSU Diagnostic Criteria May Allow Early Diagnosis
Lorenzo Saraceno, Vito A G Ricigliano, Michele Cavalli, et al.
Page
of 11