Related references
Note: Only part of the references are listed.Characteristic CSF Prion Seeding Efficiency in Humans with Prion Diseases
Maria Cramm et al.
MOLECULAR NEUROBIOLOGY (2015)
Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases
Matthias Schmitz et al.
NEUROBIOLOGY OF AGING (2014)
Early Detection of Abnormal Prion Protein in Genetic Human Prion Diseases Now Possible Using Real-Time QUIC Assay
Kazunori Sano et al.
PLOS ONE (2013)
Real time quaking-induced conversion analysis of cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease
Lynne I. McGuire et al.
ANNALS OF NEUROLOGY (2012)
Cerebrospinal fluid biomarker supported diagnosis of Creutzfeldt-Jakob disease and rapid dementias: a longitudinal multicentre study over 10 years
Katharina Stoeck et al.
BRAIN (2012)
Sporadic human prion diseases: molecular insights and diagnosis
Gianfranco Puoti et al.
LANCET NEUROLOGY (2012)
A comparison of tau and 14-3-3 protein in the diagnosis of Creutzfeldt-Jakob disease
Clive Hamlin et al.
NEUROLOGY (2012)
Diagnostic accuracy of cerebrospinal fluid protein markers for sporadic Creutzfeldt-Jakob disease in Canada: a 6-year prospective study
Michael B. Coulthart et al.
BMC NEUROLOGY (2011)
Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion
Ryuichiro Atarashi et al.
NATURE MEDICINE (2011)
Creutzfeldt-Jakob Disease Surveillance in Argentina, 1997-2008
Christian Begue et al.
NEUROEPIDEMIOLOGY (2011)
Codon 129 polymorphism and the E200K mutation do not affect the cellular prion protein isoform composition in the cerebrospinal fluid from patients with Creutzfeldt-Jakob disease
Matthias Schmitz et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2010)
The role of cerebrospinal fluid 14-3-3 and other proteins in the diagnosis of sporadic Creutzfeldt-Jakob disease in the UK: a 10-year review
G. Chohan et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2010)
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease
I. Zerr et al.
BRAIN (2009)
Diagnostic value of CSF protein profile in a Portuguese population of sCJD patients
Ines Esteves Baldeiras et al.
JOURNAL OF NEUROLOGY (2009)
Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease
S. J. Collins et al.
BRAIN (2006)
CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease
P. Sanchez-Juan et al.
NEUROLOGY (2006)
Impact of the clinical context on the 14-3-3 test for the diagnosis of sporadic CJD
Natividad Cuadrado-Corrales et al.
BMC NEUROLOGY (2006)
Effects of hemolysis and storage condition on neuron-specific enolase (NSE) in cerebrospinal fluid and serum: implications in clinical practice
L Ramont et al.
CLINICAL CHEMISTRY AND LABORATORY MEDICINE (2005)
Effects of processing and storage conditions on amyloid beta (1-42) and tau concentrations in cerebrospinal fluid: Implications for use in clinical practice
NSM Schoonenboom et al.
CLINICAL CHEMISTRY (2005)
Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease
RJ Castellani et al.
NEUROLOGY (2004)
A prospective study of CSF markers in 250 patients with possible Creutzfeldt-Jakob disease
B Van Everbroeck et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2003)
Challenging the clinical utility of the 14-3-3 protein for the diagnosis of sporadic Creutzfeldt-Jakob disease
MD Geschwind et al.
ARCHIVES OF NEUROLOGY (2003)
Use of 14-3-3 in the diagnosis of Creutzfeldt-Jakob disease
AJE Green
BIOCHEMICAL SOCIETY TRANSACTIONS (2002)
14-3-3 proteins: key regulators of cell division, signalling and apoptosis
MJ van Hemert et al.
BIOESSAYS (2001)
Use of 14-3-3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob disease
AJE Green et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2001)
Standardization of measurement of β-amyloid(1-42) in cerebrospinal fluid and plasma
H Vanderstichele et al.
AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS (2000)
Analysis of EEG and CSF 14-3-3 protein as aids to the diagnosis of Creutzfeldt-Jakob disease
I Zerr et al.
NEUROLOGY (2000)
14-3-3 testing in diagnosing Creutzfeldt-Jakob disease - A prospective study in 112 patients
AW Lemstra et al.
NEUROLOGY (2000)
Creutzfeldt-Jakob disease: diagnostic utility of 14-3-3 protein immunodetection in cerebrospinal fluid
S Collins et al.
JOURNAL OF CLINICAL NEUROSCIENCE (2000)
Share Paper
