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 (61-70 of 88) with videos related to

Pageof 9
Sort By:
Annals of Neurology|September 2, 2000
Familial Creutzfeldt-Jakob disease with a novel 120-bp insertion in the prion protein geneK H Skworc, O Windl, W J Schulz-Schaeffer, et al.
Brain : a Journal of Neurology|December 3, 1999
How to improve the clinical diagnosis of Creutzfeldt-Jakob diseaseS Poser, B Mollenhauer, A Kraubeta, et al.
BMJ (Clinical Research Ed.)|March 31, 1998
Diagnosis of Creutzfeldt-Jakob disease by measurement of S100 protein in serum: prospective case-control studyM Otto, J Wiltfang, E Schütz, 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.
Acta Neurologica Scandinavica|September 15, 2000
Creutzfeldt-Jakob disease and oxidative stressS Bleich, S Kropp, D Degner, et al.
Neurology|October 14, 2005
Sporadic Creutzfeldt-Jakob disease: clinical and diagnostic characteristics of the rare VV1 typeB Meissner, I M Westner, K Kallenberg, et al.
Journal of Neurochemistry|December 3, 1999
Isoform pattern of 14-3-3 proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob diseaseJ Wiltfang, M Otto, H C Baxter, et al.
Brain : a Journal of Neurology|May 3, 2007
Creutzfeldt-Jakob disease in Germany: a prospective 12-year surveillanceU Heinemann, A Krasnianski, B Meissner, et al.
Journal of Clinical Epidemiology|August 15, 2000
European surveillance on Creutzfeldt-Jakob disease: a case-control study for medical risk factorsI Zerr, J P Brandel, C Masullo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 10, 1999
Hashimoto's encephalitis as a differential diagnosis of Creutzfeldt-Jakob diseaseM Seipelt, I Zerr, R Nau, et al.
Pageof 9

Showing results (61-70 of 88) with videos related to

Sort By:
Pageof 9
Annals of Neurology|September 2, 2000
Familial Creutzfeldt-Jakob disease with a novel 120-bp insertion in the prion protein geneK H Skworc, O Windl, W J Schulz-Schaeffer, et al.
Brain : a Journal of Neurology|December 3, 1999
How to improve the clinical diagnosis of Creutzfeldt-Jakob diseaseS Poser, B Mollenhauer, A Kraubeta, et al.
BMJ (Clinical Research Ed.)|March 31, 1998
Diagnosis of Creutzfeldt-Jakob disease by measurement of S100 protein in serum: prospective case-control studyM Otto, J Wiltfang, E Schütz, 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.
Acta Neurologica Scandinavica|September 15, 2000
Creutzfeldt-Jakob disease and oxidative stressS Bleich, S Kropp, D Degner, et al.
Neurology|October 14, 2005
Sporadic Creutzfeldt-Jakob disease: clinical and diagnostic characteristics of the rare VV1 typeB Meissner, I M Westner, K Kallenberg, et al.
Journal of Neurochemistry|December 3, 1999
Isoform pattern of 14-3-3 proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob diseaseJ Wiltfang, M Otto, H C Baxter, et al.
Brain : a Journal of Neurology|May 3, 2007
Creutzfeldt-Jakob disease in Germany: a prospective 12-year surveillanceU Heinemann, A Krasnianski, B Meissner, et al.
Journal of Clinical Epidemiology|August 15, 2000
European surveillance on Creutzfeldt-Jakob disease: a case-control study for medical risk factorsI Zerr, J P Brandel, C Masullo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 10, 1999
Hashimoto's encephalitis as a differential diagnosis of Creutzfeldt-Jakob diseaseM Seipelt, I Zerr, R Nau, et al.
Pageof 9