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Elio Scarpini

Showing results (231-240 of 329) with videos related to

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Journal of Neurology|May 6, 2009
CCL8/MCP-2 association analysis in patients with Alzheimer's disease and frontotemporal lobar degenerationChiara Villa, Eliana Venturelli, Chiara Fenoglio, et al.
Bjpsych Open|February 2, 2021
Diogenes syndrome in dementia: a case reportLuca Sacchi, Emanuela Rotondo, Sara Pozzoli, et al.
Neuroscience Letters|April 30, 2011
GSK3β genetic variability in patients with Multiple SclerosisDaniela Galimberti, James Macmurray, Diego Scalabrini, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|November 11, 2017
The loss of macular ganglion cells begins from the early stages of disease and correlates with brain atrophy in multiple sclerosis patientsAnna M Pietroboni, Laura Dell'Arti, Michela Caprioli, et al.
Journal of Neuroimmunology|May 6, 2014
No association of IFI16 (interferon-inducible protein 16) variants with susceptibility to multiple sclerosisFranca R Guerini, Mario Clerici, Rachele Cagliani, et al.
Neuroscience Letters|November 24, 2011
MicroRNA and mRNA expression profile screening in multiple sclerosis patients to unravel novel pathogenic steps and identify potential biomarkersFilippo Martinelli-Boneschi, Chiara Fenoglio, Paola Brambilla, et al.
Journal of Neuroimmunology|May 8, 2007
ICOS gene haplotypes correlate with IL10 secretion and multiple sclerosis evolutionLuca Castelli, Cristoforo Comi, Annalisa Chiocchetti, et al.
Journal of Alzheimer'S Disease : JAD|February 26, 2013
Expression of the transcription factor Sp1 and its regulatory hsa-miR-29b in peripheral blood mononuclear cells from patients with Alzheimer's diseaseChiara Villa, Elisa Ridolfi, Chiara Fenoglio, et al.
Human Genetics|July 8, 2011
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysisRachele Cagliani, Matteo Fumagalli, Franca R Guerini, et al.
Neurology|November 17, 2017
Evidence of CNS β-amyloid deposition in Nasu-Hakola disease due to the <i>TREM2</i> Q33X mutationLaura Ghezzi, Tiziana Carandini, Andrea Arighi, et al.
Pageof 33

Showing results (231-240 of 329) with videos related to

Sort By:
Pageof 33
Journal of Neurology|May 6, 2009
CCL8/MCP-2 association analysis in patients with Alzheimer's disease and frontotemporal lobar degenerationChiara Villa, Eliana Venturelli, Chiara Fenoglio, et al.
Bjpsych Open|February 2, 2021
Diogenes syndrome in dementia: a case reportLuca Sacchi, Emanuela Rotondo, Sara Pozzoli, et al.
Neuroscience Letters|April 30, 2011
GSK3β genetic variability in patients with Multiple SclerosisDaniela Galimberti, James Macmurray, Diego Scalabrini, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|November 11, 2017
The loss of macular ganglion cells begins from the early stages of disease and correlates with brain atrophy in multiple sclerosis patientsAnna M Pietroboni, Laura Dell'Arti, Michela Caprioli, et al.
Journal of Neuroimmunology|May 6, 2014
No association of IFI16 (interferon-inducible protein 16) variants with susceptibility to multiple sclerosisFranca R Guerini, Mario Clerici, Rachele Cagliani, et al.
Neuroscience Letters|November 24, 2011
MicroRNA and mRNA expression profile screening in multiple sclerosis patients to unravel novel pathogenic steps and identify potential biomarkersFilippo Martinelli-Boneschi, Chiara Fenoglio, Paola Brambilla, et al.
Journal of Neuroimmunology|May 8, 2007
ICOS gene haplotypes correlate with IL10 secretion and multiple sclerosis evolutionLuca Castelli, Cristoforo Comi, Annalisa Chiocchetti, et al.
Journal of Alzheimer'S Disease : JAD|February 26, 2013
Expression of the transcription factor Sp1 and its regulatory hsa-miR-29b in peripheral blood mononuclear cells from patients with Alzheimer's diseaseChiara Villa, Elisa Ridolfi, Chiara Fenoglio, et al.
Human Genetics|July 8, 2011
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysisRachele Cagliani, Matteo Fumagalli, Franca R Guerini, et al.
Neurology|November 17, 2017
Evidence of CNS β-amyloid deposition in Nasu-Hakola disease due to the <i>TREM2</i> Q33X mutationLaura Ghezzi, Tiziana Carandini, Andrea Arighi, et al.
Pageof 33