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M Pocchiari

Showing results (41-50 of 63) with videos related to

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Neurology|September 1, 1996
Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation)P Barbanti, G Fabbrini, M Salvatore, et al.
Journal of Neuropathology and Experimental Neurology|November 18, 2000
Increased brain synthesis of prostaglandin E2 and F2-isoprostane in human and experimental transmissible spongiform encephalopathiesL Minghetti, A Greco, F Cardone, et al.
Brain Research Bulletin|September 14, 1999
Prion protein glycotype analysis in familial and sporadic Creutzfeldt-Jakob disease patientsF Cardone, Q G Liu, R Petraroli, et al.
Annals of Neurology|December 1, 1993
A new point mutation of the prion protein gene in Creutzfeldt-Jakob diseaseM Pocchiari, M Salvatore, F Cutruzzolá, et al.
Neurology|November 18, 1998
Fatal familial insomnia in a new Italian kindredA Padovani, M D'Alessandro, P Parchi, et al.
Hormone Research|January 11, 1991
Combination ultrafiltration and 6 M urea treatment of human growth hormone effectively minimizes risk from potential Creutzfeldt-Jakob disease virus contaminationM Pocchiari, S Peano, A Conz, et al.
Lancet (London, England)|April 6, 1996
A new variant of Creutzfeldt-Jakob disease in the UKR G Will, J W Ironside, M Zeidler, et al.
Neurology|February 1, 1994
Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicineP Brown, L Cervenáková, L G Goldfarb, et al.
Annals of Neurology|June 18, 1998
Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993-1995. EU Collaborative Study Group for CJDR G Will, A Alperovitch, S Poser, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|September 30, 2006
Quantitative profiling of the pathological prion protein allotypes in bank voles by liquid chromatography-mass spectrometryC Cartoni, M E Schininà, B Maras, et al.
Pageof 7

Showing results (41-50 of 63) with videos related to

Sort By:
Pageof 7
Neurology|September 1, 1996
Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation)P Barbanti, G Fabbrini, M Salvatore, et al.
Journal of Neuropathology and Experimental Neurology|November 18, 2000
Increased brain synthesis of prostaglandin E2 and F2-isoprostane in human and experimental transmissible spongiform encephalopathiesL Minghetti, A Greco, F Cardone, et al.
Brain Research Bulletin|September 14, 1999
Prion protein glycotype analysis in familial and sporadic Creutzfeldt-Jakob disease patientsF Cardone, Q G Liu, R Petraroli, et al.
Annals of Neurology|December 1, 1993
A new point mutation of the prion protein gene in Creutzfeldt-Jakob diseaseM Pocchiari, M Salvatore, F Cutruzzolá, et al.
Neurology|November 18, 1998
Fatal familial insomnia in a new Italian kindredA Padovani, M D'Alessandro, P Parchi, et al.
Hormone Research|January 11, 1991
Combination ultrafiltration and 6 M urea treatment of human growth hormone effectively minimizes risk from potential Creutzfeldt-Jakob disease virus contaminationM Pocchiari, S Peano, A Conz, et al.
Lancet (London, England)|April 6, 1996
A new variant of Creutzfeldt-Jakob disease in the UKR G Will, J W Ironside, M Zeidler, et al.
Neurology|February 1, 1994
Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicineP Brown, L Cervenáková, L G Goldfarb, et al.
Annals of Neurology|June 18, 1998
Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993-1995. EU Collaborative Study Group for CJDR G Will, A Alperovitch, S Poser, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|September 30, 2006
Quantitative profiling of the pathological prion protein allotypes in bank voles by liquid chromatography-mass spectrometryC Cartoni, M E Schininà, B Maras, et al.
Pageof 7