Sporadic Creutzfeldt–Jakob disease without dementia at onset: clinical features, laboratory tests and sequential diffusion MRI (in an autopsy–proven case)

Author： Pauri F.   Amabile G.   Fattapposta F.   Pierallini A.   Bianco F.  

Publisher： Springer Publishing Company

ISSN： 1590-1874

Source： Neurological Sciences, Vol.25, Iss.4, 2004-10, pp. : 234-237

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Related content

Autopsy-proven Creutzfeldt-Jakob disease in a patient with a negative 14-3-3 assay and nonspecific EEG and MRI

By Donahue J.   Hanna P.   Hariharan S.  

Neurological Sciences, Vol. 24, Iss. 6, 2004-02 ,pp. : 411-413

Springer Publishing Company

Access to resources Recommend Favorite

MRI in the diagnosis of sporadic Creutzfeldt–Jakob disease: a study on inter-observer agreement

By Tschampa Henriette J.  

Brain, Vol. 128, Iss. 9, 2005-09 ,pp. : 2026-2033

Oxford University Press

Access to resources Recommend Favorite

Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease

By Zerr I.  

Brain, Vol. 132, Iss. 10, 2009-10 ,pp. : 2659-2668

Oxford University Press

Access to resources Recommend Favorite

Clinical findings in sporadic Creutzfeldt–Jakob disease correlate with thalamic pathology

By Kretzschmar H.A.  

Brain, Vol. 125, Iss. 11, 2002-11 ,pp. : 2558-2566

Oxford University Press

Access to resources Recommend Favorite

Classification of sporadic Creutzfeldt–Jakob disease revisited

By Cali Ignazio   Castellani Rudolph   Yuan Jue   Al-Shekhlee Amer   Cohen Mark L.   Xiao Xiangzhu   Moleres Francisco J.   Parchi Piero   Zou Wen-Quan   Gambetti Pierluigi  

Brain, Vol. 129, Iss. 9, 2006-09 ,pp. : 2266-2277

Oxford University Press

Access to resources Recommend Favorite