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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 cases
Angelo 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 encephalopathy
Anna 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 controversy
Sergio Rebora, Mauro Colombo, Marjolein Breur, et al.
Annals of Neurology
|
January 27, 2006
Periodic electroencephalogram complexes in a patient with variant Creutzfeldt-Jakob disease
Simona 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 gene
Paola 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 disease
Chiara 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 Disease
Leonardo 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 gene
Gabriella Marcon, Giorgio Giaccone, Chiara Cupidi, et al.
Journal of Neurology
|
June 9, 2005
Familial frontotemporal dementia associated with the novel MAPT mutation T427M
Giorgio Giaccone, Giacomina Rossi, Laura Farina, et al.
BMJ Case Reports
|
June 21, 2011
A novel phenotype of sporadic Creutzfeldt-Jakob disease
G Giaccone, Giuseppe Di Fede, Michela Mangieri, et al.
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Search research articles
Search
Showing results (21-30 of 46) with videos related to
Sort By:
Page
of 5
Journal of Neurosurgery
|
May 6, 2005
Long-term high-frequency bilateral pallidal stimulation for neuroleptic-induced tardive dystonia. Report of two cases
Angelo 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 encephalopathy
Anna 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 controversy
Sergio Rebora, Mauro Colombo, Marjolein Breur, et al.
Annals of Neurology
|
January 27, 2006
Periodic electroencephalogram complexes in a patient with variant Creutzfeldt-Jakob disease
Simona 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 gene
Paola 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 disease
Chiara 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 Disease
Leonardo 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 gene
Gabriella Marcon, Giorgio Giaccone, Chiara Cupidi, et al.
Journal of Neurology
|
June 9, 2005
Familial frontotemporal dementia associated with the novel MAPT mutation T427M
Giorgio Giaccone, Giacomina Rossi, Laura Farina, et al.
BMJ Case Reports
|
June 21, 2011
A novel phenotype of sporadic Creutzfeldt-Jakob disease
G Giaccone, Giuseppe Di Fede, Michela Mangieri, et al.
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of 5