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Showing results (21-30 of 46) with videos related to

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Journal of Neurosurgery|May 6, 2005
Long-term high-frequency bilateral pallidal stimulation for neuroleptic-induced tardive dystonia. Report of two casesAngelo Franzini, Carlo Marras, Paolo Ferroli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 15, 2022
Correction to: The cognitive phenotypes of Creutzfeldt‑Jakob disease: comparison with secondary metabolic encephalopathyAnna Rita Giovagnoli, Giuseppe Di Fede, Giacomina Rossi, et al.
Journal of the History of the Neurosciences|October 23, 2025
Camillo Golgi and the pathology of Huntington's disease: An unresolved controversySergio Rebora, Mauro Colombo, Marjolein Breur, et al.
Annals of Neurology|January 27, 2006
Periodic electroencephalogram complexes in a patient with variant Creutzfeldt-Jakob diseaseSimona Binelli, Pamela Agazzi, Giorgio Giaccone, et al.
Archives of Neurology|October 22, 2003
A case of dementia parkinsonism resembling progressive supranuclear palsy due to mutation in the tau protein genePaola Soliveri, Giacomina Rossi, Daniela Monza, et al.
Journal of Alzheimer'S Disease : JAD|January 12, 2010
Neocortical variation of Abeta load in fully expressed, pure Alzheimer's diseaseChiara Cupidi, Raffaella Capobianco, Donato Goffredo, et al.
Molecular Neurobiology|April 30, 2017
An In Vivo <sup>11</sup>C-(R)-PK11195 PET and In Vitro Pathology Study of Microglia Activation in Creutzfeldt-Jakob DiseaseLeonardo Iaccarino, Rosa Maria Moresco, Luca Presotto, et al.
Journal of Neuropathology and Experimental Neurology|April 2, 2004
Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 geneGabriella Marcon, Giorgio Giaccone, Chiara Cupidi, et al.
Journal of Neurology|June 9, 2005
Familial frontotemporal dementia associated with the novel MAPT mutation T427MGiorgio Giaccone, Giacomina Rossi, Laura Farina, et al.
BMJ Case Reports|June 21, 2011
A novel phenotype of sporadic Creutzfeldt-Jakob diseaseG Giaccone, Giuseppe Di Fede, Michela Mangieri, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
Journal of Neurosurgery|May 6, 2005
Long-term high-frequency bilateral pallidal stimulation for neuroleptic-induced tardive dystonia. Report of two casesAngelo Franzini, Carlo Marras, Paolo Ferroli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 15, 2022
Correction to: The cognitive phenotypes of Creutzfeldt‑Jakob disease: comparison with secondary metabolic encephalopathyAnna Rita Giovagnoli, Giuseppe Di Fede, Giacomina Rossi, et al.
Journal of the History of the Neurosciences|October 23, 2025
Camillo Golgi and the pathology of Huntington's disease: An unresolved controversySergio Rebora, Mauro Colombo, Marjolein Breur, et al.
Annals of Neurology|January 27, 2006
Periodic electroencephalogram complexes in a patient with variant Creutzfeldt-Jakob diseaseSimona Binelli, Pamela Agazzi, Giorgio Giaccone, et al.
Archives of Neurology|October 22, 2003
A case of dementia parkinsonism resembling progressive supranuclear palsy due to mutation in the tau protein genePaola Soliveri, Giacomina Rossi, Daniela Monza, et al.
Journal of Alzheimer'S Disease : JAD|January 12, 2010
Neocortical variation of Abeta load in fully expressed, pure Alzheimer's diseaseChiara Cupidi, Raffaella Capobianco, Donato Goffredo, et al.
Molecular Neurobiology|April 30, 2017
An In Vivo <sup>11</sup>C-(R)-PK11195 PET and In Vitro Pathology Study of Microglia Activation in Creutzfeldt-Jakob DiseaseLeonardo Iaccarino, Rosa Maria Moresco, Luca Presotto, et al.
Journal of Neuropathology and Experimental Neurology|April 2, 2004
Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 geneGabriella Marcon, Giorgio Giaccone, Chiara Cupidi, et al.
Journal of Neurology|June 9, 2005
Familial frontotemporal dementia associated with the novel MAPT mutation T427MGiorgio Giaccone, Giacomina Rossi, Laura Farina, et al.
BMJ Case Reports|June 21, 2011
A novel phenotype of sporadic Creutzfeldt-Jakob diseaseG Giaccone, Giuseppe Di Fede, Michela Mangieri, et al.
Pageof 5