相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。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
Andre Karch et al.
JOURNAL OF NEUROLOGY (2014)
First symptom and initial diagnosis in sporadic CJD patients in Germany
Anna Krasnianski et al.
JOURNAL OF NEUROLOGY (2014)
Tau and 14-3-3 of genetic and sporadic Creutzfeldt-Jakob disease patients in Israel
Zeev Meiner et al.
JOURNAL OF NEUROLOGY (2011)
The Epidemiological, Clinical, and Laboratory Features of Sporadic Creutzfeldt-Jakob Disease Patients in China: Surveillance Data from 2006 to 2010
Chen Gao et al.
PLOS ONE (2011)
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease
I. Zerr et al.
BRAIN (2009)
Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies
Anna Ladogana et al.
JOURNAL OF NEUROLOGY (2009)
MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
R. K. Fulbright et al.
AMERICAN JOURNAL OF NEURORADIOLOGY (2008)
Fatal familial insomnia: Clinical features and early identification
Anna Krasnianski et al.
ANNALS OF NEUROLOGY (2008)
Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series
T. E. F. Webb et al.
BRAIN (2008)
Creutzfeldt-Jakob disease in Germany: a prospective 12-year surveillance
U. Heinemann et al.
BRAIN (2007)
Inherited prion disease with six octapeptide repeat insertional mutation - molecular analysis of phenotypic heterogeneity
Simon Mead et al.
BRAIN (2006)
CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease
P. Sanchez-Juan et al.
NEUROLOGY (2006)
Phenotypic variability in familial prion diseases due to the D178N mutation
JJ Zarranz et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2005)
Genetic prion disease:: the EUROCJD experience
GG Kovács et al.
HUMAN GENETICS (2005)
Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada
A Ladogana et al.
NEUROLOGY (2005)
Sporadic Creutzfeldt-Jakob disease -: Magnetic resonance imaging and clinical findings
B Meissner et al.
NEUROLOGY (2004)
Sporadic and familial CJD: classification and characterisation
P Gambetti et al.
BRITISH MEDICAL BULLETIN (2003)
Mutations of the prion protein gene -: Phenotypic spectrum
GG Kovács et al.
JOURNAL OF NEUROLOGY (2002)
Analysis of EEG and CSF 14-3-3 protein as aids to the diagnosis of Creutzfeldt-Jakob disease
I Zerr et al.
NEUROLOGY (2000)