Clinical findings and diagnosis in genetic prion diseases in Germany

Diagnostic profiles of patients with late-onset Creutzfeldt–Jakob disease differ from those of younger Creutzfeldt–Jakob patients: a historical cohort study using data from the German National Reference Center

(2014) André Karch et al.   JOURNAL OF NEUROLOGY

First symptom and initial diagnosis in sporadic CJD patients in Germany

(2014) Anna Krasnianski et al.   JOURNAL OF NEUROLOGY

The Epidemiological, Clinical, and Laboratory Features of Sporadic Creutzfeldt-Jakob Disease Patients in China: Surveillance Data from 2006 to 2010

(2011) Chen Gao et al.   PLoS One

Tau and 14-3-3 of genetic and sporadic Creutzfeldt–Jakob disease patients in Israel

(2010) Zeev Meiner et al.   JOURNAL OF NEUROLOGY

Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease

(2009) I. Zerr et al.   BRAIN

Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies

(2009) Anna Ladogana et al.   JOURNAL OF NEUROLOGY

MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study

(2008) R.K. Fulbright et al.   AMERICAN JOURNAL OF NEURORADIOLOGY

Fatal familial insomnia: Clinical features and early identification

(2008) Anna Krasnianski et al.   ANNALS OF NEUROLOGY

Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series

(2008) T. E. F. Webb et al.   BRAIN