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Daniela Galimberti

Showing results (191-200 of 526) with videos related to

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Alzheimer'S Research & Therapy|September 17, 2022
Aquaporin-4 cerebrospinal fluid levels are higher in neurodegenerative dementia: looking at glymphatic system dysregulationAndrea Arighi, Marina Arcaro, Giorgio Giulio Fumagalli, et al.
International Journal of Molecular Epidemiology and Genetics|May 4, 2011
APOE ε2 and ε4 influence the susceptibility for Alzheimer's disease but not other dementiasCarlo Lovati, Daniela Galimberti, Diego Albani, et al.
Cells|July 27, 2022
Modulation of MAPK- and PI3/AKT-Dependent Autophagy Signaling by Stavudine (D4T) in PBMC of Alzheimer's Disease PatientsFrancesca La Rosa, Chiara Paola Zoia, Chiara Bazzini, et al.
Frontiers in Neurology|February 15, 2021
Case Report: Efficacy of Rituximab in a Patient With Familial Mediterranean Fever and Multiple SclerosisMattia Pozzato, Emanuele Micaglio, Chiara Starvaggi Cucuzza, et al.
Journal of Alzheimer'S Disease : JAD|February 18, 2014
Phenotypic variability associated with the C9ORF72 hexanucleotide repeat expansion: a sporadic case of frontotemporal lobar degeneration with prodromal hyposmia and predominant semantic deficitsCarlo Abbate, Beatrice Arosio, Daniela Galimberti, et al.
Investigative Ophthalmology & Visual Science|February 4, 2021
Retinoblastoma Is Characterized by a Cold, CD8+ Cell Poor, PD-L1- Microenvironment, Which Turns Into Hot, CD8+ Cell Rich, PD-L1+ After ChemotherapyClelia Miracco, Paolo Toti, Maria Chiara Gelmi, et al.
Multiple Sclerosis and Related Disorders|August 30, 2021
In vivo evidence of functional disconnection between brainstem monoaminergic nuclei and brain networks in multiple sclerosisTiziana Carandini, Matteo Mancini, Iulia Bogdan, et al.
Antioxidants & Redox Signaling|February 6, 2013
A low-molecular-weight ferroxidase is increased in the CSF of sCJD cases: CSF ferroxidase and transferrin as diagnostic biomarkers for sCJDSwati Haldar, 'alim J Beveridge, Joseph Wong, et al.
Journal of Alzheimer'S Disease : JAD|December 16, 2020
Detection of the SQSTM1 Mutation in a Patient with Early-Onset Hippocampal Amnestic SyndromeTiziana Carandini, Luca Sacchi, Laura Ghezzi, et al.
Neurology|November 2, 2012
A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutationLaura Ghezzi, Elio Scarpini, Mario Rango, et al.
Pageof 53

Showing results (191-200 of 526) with videos related to

Sort By:
Pageof 53
Alzheimer'S Research & Therapy|September 17, 2022
Aquaporin-4 cerebrospinal fluid levels are higher in neurodegenerative dementia: looking at glymphatic system dysregulationAndrea Arighi, Marina Arcaro, Giorgio Giulio Fumagalli, et al.
International Journal of Molecular Epidemiology and Genetics|May 4, 2011
APOE ε2 and ε4 influence the susceptibility for Alzheimer's disease but not other dementiasCarlo Lovati, Daniela Galimberti, Diego Albani, et al.
Cells|July 27, 2022
Modulation of MAPK- and PI3/AKT-Dependent Autophagy Signaling by Stavudine (D4T) in PBMC of Alzheimer's Disease PatientsFrancesca La Rosa, Chiara Paola Zoia, Chiara Bazzini, et al.
Frontiers in Neurology|February 15, 2021
Case Report: Efficacy of Rituximab in a Patient With Familial Mediterranean Fever and Multiple SclerosisMattia Pozzato, Emanuele Micaglio, Chiara Starvaggi Cucuzza, et al.
Journal of Alzheimer'S Disease : JAD|February 18, 2014
Phenotypic variability associated with the C9ORF72 hexanucleotide repeat expansion: a sporadic case of frontotemporal lobar degeneration with prodromal hyposmia and predominant semantic deficitsCarlo Abbate, Beatrice Arosio, Daniela Galimberti, et al.
Investigative Ophthalmology & Visual Science|February 4, 2021
Retinoblastoma Is Characterized by a Cold, CD8+ Cell Poor, PD-L1- Microenvironment, Which Turns Into Hot, CD8+ Cell Rich, PD-L1+ After ChemotherapyClelia Miracco, Paolo Toti, Maria Chiara Gelmi, et al.
Multiple Sclerosis and Related Disorders|August 30, 2021
In vivo evidence of functional disconnection between brainstem monoaminergic nuclei and brain networks in multiple sclerosisTiziana Carandini, Matteo Mancini, Iulia Bogdan, et al.
Antioxidants & Redox Signaling|February 6, 2013
A low-molecular-weight ferroxidase is increased in the CSF of sCJD cases: CSF ferroxidase and transferrin as diagnostic biomarkers for sCJDSwati Haldar, 'alim J Beveridge, Joseph Wong, et al.
Journal of Alzheimer'S Disease : JAD|December 16, 2020
Detection of the SQSTM1 Mutation in a Patient with Early-Onset Hippocampal Amnestic SyndromeTiziana Carandini, Luca Sacchi, Laura Ghezzi, et al.
Neurology|November 2, 2012
A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutationLaura Ghezzi, Elio Scarpini, Mario Rango, et al.
Pageof 53