Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Pocchiari

Showing results (51-60 of 63) with videos related to

Pageof 7
Sort By:
Neurology|April 23, 2008
A novel PSEN2 mutation associated with a peculiar phenotypeP Piscopo, G Marcon, M R Piras, et al.
Journal of Chromatography. A|July 15, 2005
Identification of the pathological prion protein allotypes in scrapie-infected heterozygous bank voles (Clethrionomys glareolus) by high-performance liquid chromatography-mass spectrometryC Cartoni, M E Schininà, B Maras, et al.
Neurology|November 9, 2000
Iatrogenic Creutzfeldt-Jakob disease at the millenniumP Brown, M Preece, J P Brandel, et al.
European Journal of Neurology|January 26, 2008
Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's diseaseA Poleggi, A Bizzarro, A Acciarri, et al.
American Journal of Human Genetics|March 26, 1999
Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob diseaseH S Lee, N Sambuughin, L Cervenakova, et al.
Der Pathologe|March 1, 1996
[Consensus report: tissue handling in suspected Creutzfeldt-Jakob disease and other spongiform encephalopathies (prion diseases) in the human. European Union Biomed-1 Concerted Action]H Budka, A Aguzzi, P Brown, et al.
Neurology|September 20, 2000
Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob diseaseI Zerr, M Pocchiari, S Collins, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|April 21, 2012
Health professions and risk of sporadic Creutzfeldt-Jakob disease, 1965 to 2010E Alcalde-Cabero, J Almazan-Isla, J P Brandel, et al.
Journal of Neuropathology and Experimental Neurology|October 24, 1998
Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneityP Piccardo, S R Dlouhy, P M Lievens, et al.
Brain : a Journal of Neurology|September 14, 2004
Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathiesM Pocchiari, M Puopolo, E A Croes, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
Neurology|April 23, 2008
A novel PSEN2 mutation associated with a peculiar phenotypeP Piscopo, G Marcon, M R Piras, et al.
Journal of Chromatography. A|July 15, 2005
Identification of the pathological prion protein allotypes in scrapie-infected heterozygous bank voles (Clethrionomys glareolus) by high-performance liquid chromatography-mass spectrometryC Cartoni, M E Schininà, B Maras, et al.
Neurology|November 9, 2000
Iatrogenic Creutzfeldt-Jakob disease at the millenniumP Brown, M Preece, J P Brandel, et al.
European Journal of Neurology|January 26, 2008
Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's diseaseA Poleggi, A Bizzarro, A Acciarri, et al.
American Journal of Human Genetics|March 26, 1999
Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob diseaseH S Lee, N Sambuughin, L Cervenakova, et al.
Der Pathologe|March 1, 1996
[Consensus report: tissue handling in suspected Creutzfeldt-Jakob disease and other spongiform encephalopathies (prion diseases) in the human. European Union Biomed-1 Concerted Action]H Budka, A Aguzzi, P Brown, et al.
Neurology|September 20, 2000
Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob diseaseI Zerr, M Pocchiari, S Collins, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|April 21, 2012
Health professions and risk of sporadic Creutzfeldt-Jakob disease, 1965 to 2010E Alcalde-Cabero, J Almazan-Isla, J P Brandel, et al.
Journal of Neuropathology and Experimental Neurology|October 24, 1998
Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneityP Piccardo, S R Dlouhy, P M Lievens, et al.
Brain : a Journal of Neurology|September 14, 2004
Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathiesM Pocchiari, M Puopolo, E A Croes, et al.
Pageof 7