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Daniela Galimberti

Showing results (111-120 of 526) with videos related to

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International Journal of Molecular Sciences|January 13, 2015
Profiling of ubiquitination pathway genes in peripheral cells from patients with frontotemporal dementia due to C9ORF72 and GRN mutationsMaria Serpente, Chiara Fenoglio, Sara M G Cioffi, et al.
Journal of Visualized Experiments : Jove|November 3, 2016
A High Throughput, Multiplexed and Targeted Proteomic CSF Assay to Quantify Neurodegenerative Biomarkers and Apolipoprotein E Isoforms StatusWendy E Heywood, Anna Baud, Emily Bliss, et al.
European Neurology|June 13, 2009
Serotonin transporter gene polymorphic element 5-HTTLPR increases the risk of sporadic Parkinson's disease in ItalyDiego Albani, Angelica Vittori, Sara Batelli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 6, 2024
CSF sphingolipids are correlated with neuroinflammatory cytokines and differentiate neuromyelitis optica spectrum disorder from multiple sclerosisLisa Shi, Laura Ghezzi, Chiara Fenoglio, et al.
International Journal of Molecular Sciences|May 27, 2023
TREM2 Expression and Amyloid-Beta Phagocytosis in Alzheimer's DiseaseFrancesca La Rosa, Simone Agostini, Federica Piancone, et al.
Neurobiology of Aging|October 7, 2018
CSF pro-orexin and amyloid-β38 expression in Alzheimer's disease and frontotemporal dementiaWendy E Heywood, Jenny Hallqvist, Amanda J Heslegrave, et al.
Archives of Neurology|April 12, 2006
Intrathecal chemokine synthesis in mild cognitive impairment and Alzheimer diseaseDaniela Galimberti, Niki Schoonenboom, Philip Scheltens, et al.
Journal of Child Neurology|December 21, 2004
Epilepsy and electroencephalographic findings in pericentric inversion of chromosome 12Salvatore Grosso, Lucia Pucci, MariAngela Farnetani, et al.
Archives of Neurology|August 8, 2002
Hereditary neuronal intranuclear inclusion disease with autonomic failure and cerebellar degenerationRaffaella Zannolli, Sid Gilman, Simone Rossi, et al.
Journal of Neuroinflammation|June 8, 2011
Loss of function mutations in the progranulin gene are related to pro-inflammatory cytokine dysregulation in frontotemporal lobar degeneration patientsPaola Bossù, Francesca Salani, Antonella Alberici, et al.
Pageof 53

Showing results (111-120 of 526) with videos related to

Sort By:
Pageof 53
International Journal of Molecular Sciences|January 13, 2015
Profiling of ubiquitination pathway genes in peripheral cells from patients with frontotemporal dementia due to C9ORF72 and GRN mutationsMaria Serpente, Chiara Fenoglio, Sara M G Cioffi, et al.
Journal of Visualized Experiments : Jove|November 3, 2016
A High Throughput, Multiplexed and Targeted Proteomic CSF Assay to Quantify Neurodegenerative Biomarkers and Apolipoprotein E Isoforms StatusWendy E Heywood, Anna Baud, Emily Bliss, et al.
European Neurology|June 13, 2009
Serotonin transporter gene polymorphic element 5-HTTLPR increases the risk of sporadic Parkinson's disease in ItalyDiego Albani, Angelica Vittori, Sara Batelli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 6, 2024
CSF sphingolipids are correlated with neuroinflammatory cytokines and differentiate neuromyelitis optica spectrum disorder from multiple sclerosisLisa Shi, Laura Ghezzi, Chiara Fenoglio, et al.
International Journal of Molecular Sciences|May 27, 2023
TREM2 Expression and Amyloid-Beta Phagocytosis in Alzheimer's DiseaseFrancesca La Rosa, Simone Agostini, Federica Piancone, et al.
Neurobiology of Aging|October 7, 2018
CSF pro-orexin and amyloid-β38 expression in Alzheimer's disease and frontotemporal dementiaWendy E Heywood, Jenny Hallqvist, Amanda J Heslegrave, et al.
Archives of Neurology|April 12, 2006
Intrathecal chemokine synthesis in mild cognitive impairment and Alzheimer diseaseDaniela Galimberti, Niki Schoonenboom, Philip Scheltens, et al.
Journal of Child Neurology|December 21, 2004
Epilepsy and electroencephalographic findings in pericentric inversion of chromosome 12Salvatore Grosso, Lucia Pucci, MariAngela Farnetani, et al.
Archives of Neurology|August 8, 2002
Hereditary neuronal intranuclear inclusion disease with autonomic failure and cerebellar degenerationRaffaella Zannolli, Sid Gilman, Simone Rossi, et al.
Journal of Neuroinflammation|June 8, 2011
Loss of function mutations in the progranulin gene are related to pro-inflammatory cytokine dysregulation in frontotemporal lobar degeneration patientsPaola Bossù, Francesca Salani, Antonella Alberici, et al.
Pageof 53