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O Bugiani

Showing results (101-110 of 138) with videos related to

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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1991
Desferrioxamine infusion can modify EEG tracing in haemodialysed patientsD Brancaccio, G Avanzini, P Padovese, et al.
Neurology|August 10, 2000
Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP geneG Rossi, G Giaccone, L Giampaolo, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|May 19, 2000
Intracellular mechanisms mediating the neuronal death and astrogliosis induced by the prion protein fragment 106-126S Thellung, T Florio, A Corsaro, et al.
The New England Journal of Medicine|January 1, 1976
Letter: T and B lymphocytes in normal cerebrospinal fluidP E Manconi, D Zaccheo, O Bugiani, et al.
The EMBO Journal|March 1, 1991
Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58F Tagliavini, F Prelli, J Ghiso, et al.
Neurology|May 5, 1999
Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteriaN Nardocci, G Zorzi, L Farina, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1992
Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindredG Giaccone, L Verga, O Bugiani, et al.
Cancer Genetics and Cytogenetics|July 15, 1994
Increasing complexity of the karyotype in 50 human gliomas. Progressive evolution and de novo occurrence of cytogenetic alterationsI Magnani, S Guerneri, B Pollo, et al.
Biochemical and Biophysical Research Communications|August 16, 1993
Molecular characteristics of a protease-resistant, amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion proteinC Selvaggini, L De Gioia, L Cantù, et al.
Brain Pathology (Zurich, Switzerland)|April 1, 1996
Prion protein amyloidosisB Ghetti, P Piccardo, B Frangione, et al.
Pageof 14

Showing results (101-110 of 138) with videos related to

Sort By:
Pageof 14
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1991
Desferrioxamine infusion can modify EEG tracing in haemodialysed patientsD Brancaccio, G Avanzini, P Padovese, et al.
Neurology|August 10, 2000
Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP geneG Rossi, G Giaccone, L Giampaolo, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|May 19, 2000
Intracellular mechanisms mediating the neuronal death and astrogliosis induced by the prion protein fragment 106-126S Thellung, T Florio, A Corsaro, et al.
The New England Journal of Medicine|January 1, 1976
Letter: T and B lymphocytes in normal cerebrospinal fluidP E Manconi, D Zaccheo, O Bugiani, et al.
The EMBO Journal|March 1, 1991
Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58F Tagliavini, F Prelli, J Ghiso, et al.
Neurology|May 5, 1999
Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteriaN Nardocci, G Zorzi, L Farina, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1992
Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindredG Giaccone, L Verga, O Bugiani, et al.
Cancer Genetics and Cytogenetics|July 15, 1994
Increasing complexity of the karyotype in 50 human gliomas. Progressive evolution and de novo occurrence of cytogenetic alterationsI Magnani, S Guerneri, B Pollo, et al.
Biochemical and Biophysical Research Communications|August 16, 1993
Molecular characteristics of a protease-resistant, amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion proteinC Selvaggini, L De Gioia, L Cantù, et al.
Brain Pathology (Zurich, Switzerland)|April 1, 1996
Prion protein amyloidosisB Ghetti, P Piccardo, B Frangione, et al.
Pageof 14