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

I Zerr

Showing results (51-60 of 88) with videos related to

Pageof 9
Sort By:
Neuroscience|June 16, 2010
Cellular prion protein overexpression disturbs cellular homeostasis in SH-SY5Y neuroblastoma cells but does not alter p53 expression: a proteomic studyE Weiss, S Ramljak, A R Asif, et al.
Journal of Neurology|November 14, 1997
S-100 protein concentration in the cerebrospinal fluid of patients with Creutzfeldt-Jakob diseaseM Otto, H Stein, A Szudra, et al.
Neurology|August 28, 2002
Sporadic Creutzfeldt-Jakob disease and surgery: a case-control study using community controlsH J T Ward, D Everington, E A Croes, et al.
Archives of Neurology|January 29, 1999
The Heidenhain variant of Creutzfeldt-Jakob diseaseS Kropp, W J Schulz-Schaeffer, M Finkenstaedt, et al.
Human Genetics|September 15, 2000
Molecular genetics of human prion diseases in GermanyO Windl, A Giese, W Schulz-Schaeffer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 20, 2013
A proposal of new diagnostic pathway for fatal familial insomniaA Krasnianski, P Sanchez Juan, Claudia Ponto, et al.
Neurology|November 18, 1998
Phenotypic variability in fatal familial insomnia (D178N-129M) genotypeI Zerr, A Giese, O Windl, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 20, 2001
Patients with Alzheimer's disease and dementia with Lewy bodies mistaken for Creutzfeldt-Jakob diseaseH J Tschampa, M Neumann, I Zerr, et al.
Neurology|August 19, 2004
Sporadic Creutzfeldt-Jakob disease: magnetic resonance imaging and clinical findingsB Meissner, K Körtner, M Bartl, et al.
Lancet (London, England)|May 21, 1999
Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob diseaseA Alperovitch, I Zerr, M Pocchiari, et al.
Pageof 9

Showing results (51-60 of 88) with videos related to

Sort By:
Pageof 9
Neuroscience|June 16, 2010
Cellular prion protein overexpression disturbs cellular homeostasis in SH-SY5Y neuroblastoma cells but does not alter p53 expression: a proteomic studyE Weiss, S Ramljak, A R Asif, et al.
Journal of Neurology|November 14, 1997
S-100 protein concentration in the cerebrospinal fluid of patients with Creutzfeldt-Jakob diseaseM Otto, H Stein, A Szudra, et al.
Neurology|August 28, 2002
Sporadic Creutzfeldt-Jakob disease and surgery: a case-control study using community controlsH J T Ward, D Everington, E A Croes, et al.
Archives of Neurology|January 29, 1999
The Heidenhain variant of Creutzfeldt-Jakob diseaseS Kropp, W J Schulz-Schaeffer, M Finkenstaedt, et al.
Human Genetics|September 15, 2000
Molecular genetics of human prion diseases in GermanyO Windl, A Giese, W Schulz-Schaeffer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 20, 2013
A proposal of new diagnostic pathway for fatal familial insomniaA Krasnianski, P Sanchez Juan, Claudia Ponto, et al.
Neurology|November 18, 1998
Phenotypic variability in fatal familial insomnia (D178N-129M) genotypeI Zerr, A Giese, O Windl, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 20, 2001
Patients with Alzheimer's disease and dementia with Lewy bodies mistaken for Creutzfeldt-Jakob diseaseH J Tschampa, M Neumann, I Zerr, et al.
Neurology|August 19, 2004
Sporadic Creutzfeldt-Jakob disease: magnetic resonance imaging and clinical findingsB Meissner, K Körtner, M Bartl, et al.
Lancet (London, England)|May 21, 1999
Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob diseaseA Alperovitch, I Zerr, M Pocchiari, et al.
Pageof 9