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Nereo Bresolin

Showing results (321-330 of 346) with videos related to

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Journal of Alzheimer'S Disease : JAD|May 12, 2011
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasiaChiara Villa, Laura Ghezzi, Anna M Pietroboni, et al.
Journal of Cellular and Molecular Medicine|February 8, 2020
Nusinersen treatment and cerebrospinal fluid neurofilaments: An explorative study on Spinal Muscular Atrophy type 3 patientsIrene Faravelli, Megi Meneri, Domenica Saccomanno, et al.
Plos One|April 17, 2012
Progranulin gene variability and plasma levels in bipolar disorder and schizophreniaDaniela Galimberti, Bernardo Dell'Osso, Chiara Fenoglio, et al.
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|December 16, 2010
BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's diseaseEliana Venturelli, Chiara Villa, Chiara Fenoglio, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|February 23, 2012
Selective DNA methylation of BDNF promoter in bipolar disorder: differences among patients with BDI and BDIIClaudio D'Addario, Bernardo Dell'Osso, Maria Carlotta Palazzo, 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.
Plos One|April 15, 2016
Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot StudyAndrea Martinuzzi, Domenico Montanaro, Marinela Vavla, et al.
Journal of Molecular Neuroscience : MN|April 24, 2016
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian PatientsDaniela Piga, Francesca Magri, Dario Ronchi, et al.
Cellular and Molecular Life Sciences : CMLS|November 25, 2023
Combined RNA interference and gene replacement therapy targeting MFN2 as proof of principle for the treatment of Charcot-Marie-Tooth type 2AFederica Rizzo, Silvia Bono, Marc David Ruepp, et al.
Pageof 35

Showing results (321-330 of 346) with videos related to

Sort By:
Pageof 35
Journal of Alzheimer'S Disease : JAD|May 12, 2011
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasiaChiara Villa, Laura Ghezzi, Anna M Pietroboni, et al.
Journal of Cellular and Molecular Medicine|February 8, 2020
Nusinersen treatment and cerebrospinal fluid neurofilaments: An explorative study on Spinal Muscular Atrophy type 3 patientsIrene Faravelli, Megi Meneri, Domenica Saccomanno, et al.
Plos One|April 17, 2012
Progranulin gene variability and plasma levels in bipolar disorder and schizophreniaDaniela Galimberti, Bernardo Dell'Osso, Chiara Fenoglio, et al.
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|December 16, 2010
BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's diseaseEliana Venturelli, Chiara Villa, Chiara Fenoglio, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|February 23, 2012
Selective DNA methylation of BDNF promoter in bipolar disorder: differences among patients with BDI and BDIIClaudio D'Addario, Bernardo Dell'Osso, Maria Carlotta Palazzo, 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.
Plos One|April 15, 2016
Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot StudyAndrea Martinuzzi, Domenico Montanaro, Marinela Vavla, et al.
Journal of Molecular Neuroscience : MN|April 24, 2016
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian PatientsDaniela Piga, Francesca Magri, Dario Ronchi, et al.
Cellular and Molecular Life Sciences : CMLS|November 25, 2023
Combined RNA interference and gene replacement therapy targeting MFN2 as proof of principle for the treatment of Charcot-Marie-Tooth type 2AFederica Rizzo, Silvia Bono, Marc David Ruepp, et al.
Pageof 35