4.7 Review

Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease

Related references

Note: Only part of the references are listed.
Article Biochemistry & Molecular Biology

High Diagnostic Accuracy of RT-QuIC Assay in a Prospective Study of Patients with Suspected sCJD

Michele Fiorini et al.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2020)

Article Clinical Neurology

Detection of prions in skin punch biopsies of Creutzfeldt-Jakob disease patients

Angela Mammana et al.

ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY (2020)

Review Clinical Neurology

Towards a treatment for genetic prion disease: trials and biomarkers

Sonia M. Vallabh et al.

LANCET NEUROLOGY (2020)

Article Clinical Neurology

A prognostic model for overall survival in sporadic Creutzfeldt-Jakob disease

Franc Llorens et al.

ALZHEIMERS & DEMENTIA (2020)

Article Medicine, General & Internal

Cerebrospinal fluid and plasma biomarkers in individuals at risk for genetic prion disease

Sonia M. Vallabh et al.

BMC MEDICINE (2020)

Article Clinical Neurology

Transmission of CJD from nasal brushings but not spinal fluid or RT-QuIC product

Gregory J. Raymond et al.

ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY (2020)

Article Clinical Neurology

Diagnosis of prion diseases by RT-QuIC results in improved surveillance

Daniel D. Rhoads et al.

NEUROLOGY (2020)

Article Clinical Neurology

Comparison between plasma and cerebrospinal fluid biomarkers for the early diagnosis and association with survival in prion disease

Samir Abu-Rumeileh et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2020)

Article Neurosciences

Cerebrospinal Fluid Total Prion Protein in the Spectrum of Prion Diseases

Anna Villar-Pique et al.

MOLECULAR NEUROBIOLOGY (2019)

Article Clinical Neurology

Cerebrospinal fluid neurofilament light in suspected sporadic Creutzfeldt-Jakob disease

Eirini Kanata et al.

JOURNAL OF CLINICAL NEUROSCIENCE (2019)

Article Multidisciplinary Sciences

Prion protein quantification in human cerebrospinal fluid as a tool for prion disease drug development

Sonia M. Vallabh et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2019)

Article Medical Laboratory Technology

Diagnosis associated with Tau higher than 1200 pg/mL: Insights from the clinical and laboratory practice

S. Lehmann et al.

CLINICA CHIMICA ACTA (2019)

Article Biochemical Research Methods

Domain-specific Quantification of Prion Protein in Cerebrospinal Fluid by Targeted Mass Spectrometry

Eric Vallabh Minikel et al.

MOLECULAR & CELLULAR PROTEOMICS (2019)

Article Clinical Neurology

Diagnostic value of surrogate CSF biomarkers for Creutzfeldt-Jakob disease in the era of RT-QuIC

Samir Abu-Rumeileh et al.

JOURNAL OF NEUROLOGY (2019)

Article Clinical Neurology

Imaging and CSF analyses effectively distinguish CJD from its mimics

Peter Rudge et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2018)

Article Neurosciences

Validation of α-Synuclein as a CSF Biomarker for Sporadic Creutzfeldt-Jakob Disease

Franc Llorens et al.

MOLECULAR NEUROBIOLOGY (2018)

Article Clinical Neurology

The CSF neurofilament light signature in rapidly progressive neurodegenerative dementias

Samir Abu-Rumeileh et al.

ALZHEIMERS RESEARCH & THERAPY (2018)

Article Clinical Neurology

Sporadic Fatal Insomnia in Europe: Phenotypic Features and Diagnostic Challenges

Samir Abu-Rumeileh et al.

ANNALS OF NEUROLOGY (2018)

Article Pathology

Rapid amplification of prions from variant Creutzfeldt-Jakob disease cerebrospinal fluid

Marcelo A. Barria et al.

JOURNAL OF PATHOLOGY CLINICAL RESEARCH (2018)

Article Clinical Neurology

Extended and direct evaluation of RT-QuIC assays for Creutzfeldt-Jakob disease diagnosis

Bradley R. Groveman et al.

ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY (2017)

Article Biochemistry & Molecular Biology

FDG-PET in Creutzfeldt-Jakob disease: Analysis of clinical-PET correlation

Dimitri Renard et al.

PRION (2017)

Article Cell Biology

Prion seeding activity and infectivity in skin samples from patients with sporadic Creutzfeldt-Jakob disease

Christina D. Orru et al.

SCIENCE TRANSLATIONAL MEDICINE (2017)

Review Clinical Neurology

Neuroimaging in Dementia

Adam M. Staffaroni et al.

SEMINARS IN NEUROLOGY (2017)

Article Multidisciplinary Sciences

High diagnostic value of second generation CSF RT-QuIC across the wide spectrum of CJD prions

Alessia Franceschini et al.

SCIENTIFIC REPORTS (2017)

Article Geriatrics & Gerontology

Cerebrospinal Fluid Biomarker-Based Diagnosis of Sporadic Creutzfeldt-Jakob Disease: A Validation Study for Previously Established Cutoffs

Franc Llorens et al.

DEMENTIA AND GERIATRIC COGNITIVE DISORDERS (2017)

Article Clinical Neurology

Diagnostic and prognostic value of human prion detection in cerebrospinal fluid

Aaron Foutz et al.

ANNALS OF NEUROLOGY (2017)

Article Clinical Neurology

CSF tau correlates with CJD disease severity and cognitive decline

O. S. Cohen et al.

ACTA NEUROLOGICA SCANDINAVICA (2016)

Article Neurosciences

Validation of 14-3-3 Protein as a Marker in Sporadic Creutzfeldt-Jakob Disease Diagnostic

Matthias Schmitz et al.

MOLECULAR NEUROBIOLOGY (2016)

Review Neurosciences

Tau in physiology and pathology

Yipeng Wang et al.

NATURE REVIEWS NEUROSCIENCE (2016)

Article Clinical Neurology

Long-Term Preclinical Magnetic Resonance Imaging Alterations in Sporadic Creutzfeldt-Jakob Disease

Gianluigi Zanusso et al.

ANNALS OF NEUROLOGY (2016)

Article Clinical Neurology

Real-Time Quaking-Induced Conversion Analysis for the Diagnosis of Sporadic Creutzfeldt-Jakob Disease in Korea

Jeong-Ho Park et al.

JOURNAL OF CLINICAL NEUROLOGY (2016)

Article Clinical Neurology

Quantitative EEG parameters correlate with the progression of human prion diseases

Edit Franko et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2016)

Review Clinical Neurology

Advanced tests for early and accurate diagnosis of Creutzfeldt-Jakob disease

Gianluigi Zanusso et al.

NATURE REVIEWS NEUROLOGY (2016)

Article Cell Biology

Detection of prions in blood from patients with variant Creutzfeldt-Jakob disease

Luis Concha-Marambio et al.

SCIENCE TRANSLATIONAL MEDICINE (2016)

Article Multidisciplinary Sciences

Neurofilaments in blood and CSF for diagnosis and prediction of onset in Creutzfeldt-Jakob disease

Petra Steinacker et al.

SCIENTIFIC REPORTS (2016)

Article Geriatrics & Gerontology

Cerebrospinal fluid tau levels are a marker for molecular subtype in sporadic Creutzfeldt-Jakob disease

Andre Karch et al.

NEUROBIOLOGY OF AGING (2015)

Article Clinical Neurology

White matter involvement in sporadic Creutzfeldt-Jakob disease

Eduardo Caverzasi et al.

BRAIN (2014)

Article Medicine, General & Internal

A Test for Creutzfeldt-Jakob Disease Using Nasal Brushings

Christina D. Orru et al.

NEW ENGLAND JOURNAL OF MEDICINE (2014)

Article Medicine, General & Internal

Prions in the Urine of Patients with Variant Creutzfeldt- Jakob Disease

Fabio Moda et al.

NEW ENGLAND JOURNAL OF MEDICINE (2014)

Article Clinical Neurology

MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease

Christopher Carswell et al.

BMC NEUROLOGY (2012)

Article Clinical Neurology

Serum tau protein as a marker for the diagnosis of Creutzfeldt-Jakob disease

Moeko Noguchi-Shinohara et al.

JOURNAL OF NEUROLOGY (2011)

Article Biochemistry & Molecular Biology

Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion

Ryuichiro Atarashi et al.

NATURE MEDICINE (2011)

Article Clinical Neurology

Sporadic Creutzfeldt-Jakob disease mimicking nonconvulsive status epilepticus

B. Lapergue et al.

NEUROLOGY (2010)

Article Biochemical Research Methods

Ultrasensitive detection of scrapie prion protein using seeded conversion of recombinant prion protein

Ryuichiro Atarashi et al.

NATURE METHODS (2007)

Article Clinical Neurology

CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease

P. Sanchez-Juan et al.

NEUROLOGY (2006)

Article Clinical Neurology

Neurofilament phosphoforms: Surrogate markers for axonal injury, degeneration and loss

A Petzold

JOURNAL OF THE NEUROLOGICAL SCIENCES (2005)

Article Clinical Neurology

Diagnostic value of periodic complexes in Creutzfeldt-Jakob disease

BJ Steinhoff et al.

ANNALS OF NEUROLOGY (2004)

Review Neurosciences

14-3-3 proteins in the nervous system

D Berg et al.

NATURE REVIEWS NEUROSCIENCE (2003)

Article Biochemistry & Molecular Biology

Phospho-tau/total tau ratio in cerebrospinal fluid discriminates Creutzfeldt-Jakob disease from other dementias

M Riemenschneider et al.

MOLECULAR PSYCHIATRY (2003)