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Orphanet Journal of Rare Diseases|March 29, 2024
The pathology of X-linked adrenoleukodystrophy: tissue specific changes as a clue to pathophysiologyHemmo A F Yska, Marc Engelen, Marianna Bugiani
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 29, 2011
Scurvy hidden behind neuropsychiatric symptomsMargherita Estienne, Marianna Bugiani, Alberto Bizzi, et al.
Neuromodulation : Journal of the International Neuromodulation Society|December 14, 2011
Hamilton rating scale for depression-21 modifications in patients with vagal nerve stimulation for treatment of treatment-resistant depression: series reportAngelo Franzini, Giuseppe Messina, Carlo Marras, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 28, 2022
The cognitive phenotypes of Creutzfeldt-Jakob disease: comparison with secondary metabolic encephalopathyAnna Rita Giovagnoli, Giuseppe Di Fede, Giacomina Rossi, et al.
Journal of Alzheimer'S Disease : JAD|July 16, 2014
A mutation in the 5'-UTR of GRN gene associated with frontotemporal lobar degeneration: phenotypic variability and possible pathogenetic mechanismsGianfranco Puoti, Maria Cristina Lerza, Maria Giulia Ferretti, et al.
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.
Annals of Neurology|January 27, 2006
Periodic electroencephalogram complexes in a patient with variant Creutzfeldt-Jakob diseaseSimona Binelli, Pamela Agazzi, Giorgio Giaccone, et al.
Handbook of Clinical Neurology|September 25, 2024
Vanishing white matterMarjo S van der Knaap, Marianna Bugiani, Truus E M Abbink
Brain Pathology (Zurich, Switzerland)|May 10, 2018
Vanishing white matter: a leukodystrophy due to astrocytic dysfunctionMarianna Bugiani, Caroline Vuong, Marjolein Breur, 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.
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