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I Zerr

Showing results (41-50 of 88) with videos related to

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Lancet (London, England)|September 28, 1996
Diagnosis of Creutzfeldt-Jakob disease by two-dimensional gel electrophoresis of cerebrospinal fluidI Zerr, M Bodemer, M Otto, et al.
Archives of Neurology|February 1, 1996
Accuracy and reliability of periodic sharp wave complexes in Creutzfeldt-Jakob diseaseB J Steinhoff, S Räcker, G Herrendorf, et al.
AJNR. American Journal of Neuroradiology|July 5, 2008
Isolated cortical signal increase on MR imaging as a frequent lesion pattern in sporadic Creutzfeldt-Jakob diseaseB Meissner, K Kallenberg, P Sanchez-Juan, et al.
Transfusion|April 24, 2001
Immunochemical determination of cellular prion protein in plasma from healthy subjects and patients with sporadic CJD or other neurologic diseasesD Völkel, K Zimmermann, I Zerr, et al.
Neuroscience Letters|March 19, 1999
Increase of neuron-specific enolase in patients with Creutzfeldt-Jakob diseaseS Kropp, I Zerr, W J Schulz-Schaeffer, et al.
AJNR. American Journal of Neuroradiology|August 16, 2006
Creutzfeldt-Jakob disease: comparative analysis of MR imaging sequencesK Kallenberg, W J Schulz-Schaeffer, U Jastrow, et al.
Neuroscience Letters|April 11, 1997
Elevated levels of tau-protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob diseaseM Otto, J Wiltfang, H Tumani, et al.
Human Genetics|November 10, 2001
Polymorphisms within the prion-like protein gene (Prnd) and their implications in human prion diseases, Alzheimer's disease and other neurological disordersB Schröder, B Franz, P Hempfling, et al.
Annals of Neurology|February 5, 1998
Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob diseaseI Zerr, M Bodemer, O Gefeller, et al.
Journal of Medical Genetics|October 19, 2006
Significant association of a M129V independent polymorphism in the 5' UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control studyC Vollmert, O Windl, W Xiang, et al.
Pageof 9

Showing results (41-50 of 88) with videos related to

Sort By:
Pageof 9
Lancet (London, England)|September 28, 1996
Diagnosis of Creutzfeldt-Jakob disease by two-dimensional gel electrophoresis of cerebrospinal fluidI Zerr, M Bodemer, M Otto, et al.
Archives of Neurology|February 1, 1996
Accuracy and reliability of periodic sharp wave complexes in Creutzfeldt-Jakob diseaseB J Steinhoff, S Räcker, G Herrendorf, et al.
AJNR. American Journal of Neuroradiology|July 5, 2008
Isolated cortical signal increase on MR imaging as a frequent lesion pattern in sporadic Creutzfeldt-Jakob diseaseB Meissner, K Kallenberg, P Sanchez-Juan, et al.
Transfusion|April 24, 2001
Immunochemical determination of cellular prion protein in plasma from healthy subjects and patients with sporadic CJD or other neurologic diseasesD Völkel, K Zimmermann, I Zerr, et al.
Neuroscience Letters|March 19, 1999
Increase of neuron-specific enolase in patients with Creutzfeldt-Jakob diseaseS Kropp, I Zerr, W J Schulz-Schaeffer, et al.
AJNR. American Journal of Neuroradiology|August 16, 2006
Creutzfeldt-Jakob disease: comparative analysis of MR imaging sequencesK Kallenberg, W J Schulz-Schaeffer, U Jastrow, et al.
Neuroscience Letters|April 11, 1997
Elevated levels of tau-protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob diseaseM Otto, J Wiltfang, H Tumani, et al.
Human Genetics|November 10, 2001
Polymorphisms within the prion-like protein gene (Prnd) and their implications in human prion diseases, Alzheimer's disease and other neurological disordersB Schröder, B Franz, P Hempfling, et al.
Annals of Neurology|February 5, 1998
Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob diseaseI Zerr, M Bodemer, O Gefeller, et al.
Journal of Medical Genetics|October 19, 2006
Significant association of a M129V independent polymorphism in the 5' UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control studyC Vollmert, O Windl, W Xiang, et al.
Pageof 9