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D Galimberti

Showing results (41-50 of 64) with videos related to

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European Journal of Neurology|November 29, 2007
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degenerationE Venturelli, C Villa, E Scarpini, et al.
European Journal of Neurology|August 30, 2008
Novel exon 1 progranulin gene variant in Alzheimer's diseaseF Cortini, C Fenoglio, I Guidi, et al.
Epidemiology and Infection|September 27, 2005
Rubella and measles seroprevalence among women of childbearing age, Argentina, 2002G H Dayan, M S Panero, A Urquiza, et al.
Neuro-Degenerative Diseases|January 21, 2012
Pin1 contribution to Alzheimer's disease: transcriptional and epigenetic mechanisms in patients with late-onset Alzheimer's diseaseB Arosio, A Bulbarelli, S Bastias Candia, et al.
Geroscience|February 1, 2023
Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effectC Visconte, M T Golia, C Fenoglio, et al.
AJNR. American Journal of Neuroradiology|February 27, 2016
Hemodynamic and Anatomic Variations Require an Adaptable Approach during Intra-Arterial Chemotherapy for Intraocular Retinoblastoma: Alternative Routes, Strategies, and Follow-UpE Bertelli, S Leonini, D Galimberti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 15, 2016
The Italian dementia with Lewy bodies study group (DLB-SINdem): toward a standardization of clinical procedures and multicenter cohort studies designL Bonanni, A Cagnin, F Agosta, et al.
European Journal of Neurology|March 27, 2015
EFNS-ENS/EAN Guideline on concomitant use of cholinesterase inhibitors and memantine in moderate to severe Alzheimer's diseaseR Schmidt, E Hofer, F H Bouwman, et al.
European Journal of Neurology|January 14, 2010
Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohortF Martinelli-Boneschi, F Esposito, D Scalabrini, et al.
European Journal of Neurology|December 18, 2008
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degenerationE Venturelli, C Villa, C Fenoglio, et al.
Pageof 7

Showing results (41-50 of 64) with videos related to

Sort By:
Pageof 7
European Journal of Neurology|November 29, 2007
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degenerationE Venturelli, C Villa, E Scarpini, et al.
European Journal of Neurology|August 30, 2008
Novel exon 1 progranulin gene variant in Alzheimer's diseaseF Cortini, C Fenoglio, I Guidi, et al.
Epidemiology and Infection|September 27, 2005
Rubella and measles seroprevalence among women of childbearing age, Argentina, 2002G H Dayan, M S Panero, A Urquiza, et al.
Neuro-Degenerative Diseases|January 21, 2012
Pin1 contribution to Alzheimer's disease: transcriptional and epigenetic mechanisms in patients with late-onset Alzheimer's diseaseB Arosio, A Bulbarelli, S Bastias Candia, et al.
Geroscience|February 1, 2023
Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effectC Visconte, M T Golia, C Fenoglio, et al.
AJNR. American Journal of Neuroradiology|February 27, 2016
Hemodynamic and Anatomic Variations Require an Adaptable Approach during Intra-Arterial Chemotherapy for Intraocular Retinoblastoma: Alternative Routes, Strategies, and Follow-UpE Bertelli, S Leonini, D Galimberti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 15, 2016
The Italian dementia with Lewy bodies study group (DLB-SINdem): toward a standardization of clinical procedures and multicenter cohort studies designL Bonanni, A Cagnin, F Agosta, et al.
European Journal of Neurology|March 27, 2015
EFNS-ENS/EAN Guideline on concomitant use of cholinesterase inhibitors and memantine in moderate to severe Alzheimer's diseaseR Schmidt, E Hofer, F H Bouwman, et al.
European Journal of Neurology|January 14, 2010
Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohortF Martinelli-Boneschi, F Esposito, D Scalabrini, et al.
European Journal of Neurology|December 18, 2008
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degenerationE Venturelli, C Villa, C Fenoglio, et al.
Pageof 7