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Annals of Neurology|February 9, 2000
Creutzfeldt-Jakob disease profile in patients homozygous for the PRNP E200K mutationE S Simon, E Kahana, J Chapman, et al.
AJNR. American Journal of Neuroradiology|May 12, 2012
Cerebral white matter disruption in Creutzfeldt-Jakob diseaseH Lee, O S Cohen, H Rosenmann, et al.
European Journal of Neurology|February 2, 2010
Rapidly progressive Creutzfeldt-Jakob disease in patients with Familial Mediterranean FeverS A Appel, J Chapman, E Kahana, et al.
European Journal of Neurology|December 10, 2019
Pseudo-anticipation in Creutzfeldt-Jakob disease is due to a rhomboid-shaped artifactO S Cohen, E Kahana, A D Korczyn, et al.
Acta Neurologica Scandinavica|May 28, 2015
CSF tau correlates with CJD disease severity and cognitive declineO S Cohen, J Chapman, A D Korczyn, et al.
European Journal of Neurology|January 26, 2016
Unusual presentations in patients with E200K familial Creutzfeldt-Jakob diseaseO S Cohen, I Kimiagar, A D Korczyn, et al.
Molecular Medicine (Cambridge, Mass.)|September 1, 1995
Complete penetrance of Creutzfeldt-Jakob disease in Libyan Jews carrying the E200K mutation in the prion protein geneS Spudich, J A Mastrianni, M Wrensch, et al.
American Journal of Medical Genetics|April 15, 2000
Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammationE M McNally, C T Ly, H Rosenmann, et al.
Acta Neurologica Scandinavica|February 10, 2011
The Creutzfeldt-Jakob disease (CJD) neurological status scale: a new tool for evaluation of disease severity and progressionO S Cohen, I Prohovnik, A D Korczyn, et al.
Brain : a Journal of Neurology|May 29, 2000
Muscular dystrophy due to dysferlin deficiency in Libyan Jews. Clinical and genetic featuresZ Argov, M Sadeh, K Mazor, et al.
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