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I Zerr

Showing results (71-80 of 88) with videos related to

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European Journal of Neurology|August 8, 2008
MRI in the classical MM1 and the atypical MV2 subtypes of sporadic CJD: an inter-observer agreement studyA Krasnianski, K Kallenberg, D A Collie, et al.
Neurology|March 17, 2000
Decreased beta-amyloid1-42 in cerebrospinal fluid of patients with Creutzfeldt-Jakob diseaseM Otto, H Esselmann, W Schulz-Shaeffer, et al.
Journal of Neurology|January 23, 2009
MRI and clinical syndrome in dura mater-related Creutzfeldt-Jakob diseaseB Meissner, K Kallenberg, P Sanchez-Juan, et al.
Annals of Neurology|September 8, 2000
Current clinical diagnosis in Creutzfeldt-Jakob disease: identification of uncommon variantsI Zerr, W J Schulz-Schaeffer, A Giese, et al.
Neuropathology and Applied Neurobiology|June 20, 2019
Plasma total prion protein as a potential biomarker for neurodegenerative dementia: diagnostic accuracy in the spectrum of prion diseasesF Llorens, A Villar-Piqué, M Schmitz, et al.
Neurology|November 9, 2000
Iatrogenic Creutzfeldt-Jakob disease at the millenniumP Brown, M Preece, J P Brandel, et al.
Annals of Neurology|August 12, 1999
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjectsP Parchi, A Giese, S Capellari, et al.
Lancet (London, England)|July 11, 1998
Case-control study of risk factors of Creutzfeldt-Jakob disease in Europe during 1993-95. European Union (EU) Collaborative Study Group of Creutzfeldt-Jakob disease (CJD)C M van Duijn, N Delasnerie-Lauprêtre, C Masullo, et al.
European Journal of Neurology|January 26, 2007
CSF analysis in patients with sporadic CJD and other transmissible spongiform encephalopathiesA Green, P Sanchez-Juan, A Ladogana, et al.
Neurology|June 10, 2009
MRI lesion profiles in sporadic Creutzfeldt-Jakob diseaseB Meissner, K Kallenberg, P Sanchez-Juan, et al.
Pageof 9

Showing results (71-80 of 88) with videos related to

Sort By:
Pageof 9
European Journal of Neurology|August 8, 2008
MRI in the classical MM1 and the atypical MV2 subtypes of sporadic CJD: an inter-observer agreement studyA Krasnianski, K Kallenberg, D A Collie, et al.
Neurology|March 17, 2000
Decreased beta-amyloid1-42 in cerebrospinal fluid of patients with Creutzfeldt-Jakob diseaseM Otto, H Esselmann, W Schulz-Shaeffer, et al.
Journal of Neurology|January 23, 2009
MRI and clinical syndrome in dura mater-related Creutzfeldt-Jakob diseaseB Meissner, K Kallenberg, P Sanchez-Juan, et al.
Annals of Neurology|September 8, 2000
Current clinical diagnosis in Creutzfeldt-Jakob disease: identification of uncommon variantsI Zerr, W J Schulz-Schaeffer, A Giese, et al.
Neuropathology and Applied Neurobiology|June 20, 2019
Plasma total prion protein as a potential biomarker for neurodegenerative dementia: diagnostic accuracy in the spectrum of prion diseasesF Llorens, A Villar-Piqué, M Schmitz, et al.
Neurology|November 9, 2000
Iatrogenic Creutzfeldt-Jakob disease at the millenniumP Brown, M Preece, J P Brandel, et al.
Annals of Neurology|August 12, 1999
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjectsP Parchi, A Giese, S Capellari, et al.
Lancet (London, England)|July 11, 1998
Case-control study of risk factors of Creutzfeldt-Jakob disease in Europe during 1993-95. European Union (EU) Collaborative Study Group of Creutzfeldt-Jakob disease (CJD)C M van Duijn, N Delasnerie-Lauprêtre, C Masullo, et al.
European Journal of Neurology|January 26, 2007
CSF analysis in patients with sporadic CJD and other transmissible spongiform encephalopathiesA Green, P Sanchez-Juan, A Ladogana, et al.
Neurology|June 10, 2009
MRI lesion profiles in sporadic Creutzfeldt-Jakob diseaseB Meissner, K Kallenberg, P Sanchez-Juan, et al.
Pageof 9