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Brain Pathology (Zurich, Switzerland)|April 17, 2001
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophyG Zanusso, G Vattemi, S Ferrari, et al.Journal of Neurology, Neurosurgery, and Psychiatry|September 19, 2009
The oldest old Creutzfeldt-Jakob disease caseM Buganza, S Ferrari, M E Cecchini, et al.Journal of Neuropathology and Experimental Neurology|September 1, 1992
Inherited neuroaxonal dystrophy in C6 deficient rabbitsC Giannini, S Monaco, M Kirschfink, et al.Neurology|May 11, 2005
Phosphorylated 14-3-3zeta protein in the CSF of neuroleptic-treated patientsG Zanusso, M Fiorini, A Farinazzo, et al.The Journal of Biological Chemistry|October 30, 2001
pH-dependent prion protein conformation in classical Creutzfeldt-Jakob diseaseG Zanusso, A Farinazzo, M Fiorini, et al.Journal of Neuroimmunology|March 1, 1997
T-cell-mediated epineurial vasculitis and humoral-mediated microangiopathy in cryoglobulinemic neuropathyB Bonetti, F Invernizzi, N Rizzuto, et al.Neurology|March 1, 1988
Polyneuropathy in hypereosinophilic syndromeS Monaco, B Lucci, N Laperchia, et al.Acta Neuropathologica|December 9, 1998
Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelinS Ferrari, M Morbin, E Nobile-Orazio, et al.Neuropathology and Applied Neurobiology|December 1, 1993
IDPN impairs post-traumatic regeneration of rat sciatic nerveM Morbin, S Monaco, G Zanette, et al.Rivista Di Patologia Nervosa E Mentale|May 1, 1982
[Hypertrophic neuropathies beginning in infancy: a study of 3 cases (author's transl)]S Monaco, G Moretto, L Pinelli, et al.Pageof 103