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Boneschi

Showing results (251-260 of 310) with videos related to

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Journal of Alzheimer'S Disease : JAD|June 29, 2011
Role of OLR1 and its regulating hsa-miR369-3p in Alzheimer's disease: genetics and expression analysisMaria Serpente, Chiara Fenoglio, Chiara Villa, et al.
Journal of Alzheimer'S Disease : JAD|June 18, 2010
Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patientsFrancesco Lescai, Chiara Pirazzini, Giuseppe D'Agostino, et al.
Journal of Neurology|October 13, 2001
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluationM Sciacco, A Prelle, G P Comi, et al.
Journal of Alzheimer'S Disease : JAD|January 12, 2010
GRN variability contributes to sporadic frontotemporal lobar degenerationDaniela Galimberti, Chiara Fenoglio, Francesca Cortini, et al.
Brain Connectivity|January 31, 2023
European Working Group on SARS-CoV-2: Current Understanding, Unknowns, and Recommendations on the Neurological Complications of COVID-19Harry Crook, Alfredo Ramirez, Akram Hosseini, et al.
Rejuvenation Research|May 10, 2011
Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with Alzheimer disease and frontotemporal lobar degenerationChiara Villa, Chiara Fenoglio, Milena De Riz, et al.
Journal of the Neurological Sciences|May 18, 2021
Impact of SARS-CoV-2 infection on acute intracerebral haemorrhage in northern ItalyDavide Sangalli, Filippo Martinelli-Boneschi, Maurizio Versino, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|November 27, 2013
Genetic burden of common variants in progressive and bout-onset multiple sclerosisMelissa Sorosina, Paola Brambilla, Ferdinando Clarelli, et al.
Frontiers in Genetics|January 20, 2022
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental PopulationFerdinando Clarelli, Nadia Barizzone, Eleonora Mangano, et al.
Journal of Neuroimmunology|December 18, 2021
Burden of rare coding variants in an Italian cohort of familial multiple sclerosisE Mascia, F Clarelli, A Zauli, et al.
Pageof 31

Showing results (251-260 of 310) with videos related to

Sort By:
Pageof 31
Journal of Alzheimer'S Disease : JAD|June 29, 2011
Role of OLR1 and its regulating hsa-miR369-3p in Alzheimer's disease: genetics and expression analysisMaria Serpente, Chiara Fenoglio, Chiara Villa, et al.
Journal of Alzheimer'S Disease : JAD|June 18, 2010
Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patientsFrancesco Lescai, Chiara Pirazzini, Giuseppe D'Agostino, et al.
Journal of Neurology|October 13, 2001
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluationM Sciacco, A Prelle, G P Comi, et al.
Journal of Alzheimer'S Disease : JAD|January 12, 2010
GRN variability contributes to sporadic frontotemporal lobar degenerationDaniela Galimberti, Chiara Fenoglio, Francesca Cortini, et al.
Brain Connectivity|January 31, 2023
European Working Group on SARS-CoV-2: Current Understanding, Unknowns, and Recommendations on the Neurological Complications of COVID-19Harry Crook, Alfredo Ramirez, Akram Hosseini, et al.
Rejuvenation Research|May 10, 2011
Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with Alzheimer disease and frontotemporal lobar degenerationChiara Villa, Chiara Fenoglio, Milena De Riz, et al.
Journal of the Neurological Sciences|May 18, 2021
Impact of SARS-CoV-2 infection on acute intracerebral haemorrhage in northern ItalyDavide Sangalli, Filippo Martinelli-Boneschi, Maurizio Versino, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|November 27, 2013
Genetic burden of common variants in progressive and bout-onset multiple sclerosisMelissa Sorosina, Paola Brambilla, Ferdinando Clarelli, et al.
Frontiers in Genetics|January 20, 2022
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental PopulationFerdinando Clarelli, Nadia Barizzone, Eleonora Mangano, et al.
Journal of Neuroimmunology|December 18, 2021
Burden of rare coding variants in an Italian cohort of familial multiple sclerosisE Mascia, F Clarelli, A Zauli, et al.
Pageof 31