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。Palliative care in Creutzfeldt-Jakob disease: looking back, thinking ahead
Kay De Vries et al.
BMJ SUPPORTIVE & PALLIATIVE CARE (2021)
Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease
Peter Hermann et al.
LANCET NEUROLOGY (2021)
The importance of ongoing international surveillance for Creutzfeldt-Jakob disease
Neil Watson et al.
NATURE REVIEWS NEUROLOGY (2021)
Evaluation of a New Criterion for Detecting Prion Disease With Diffusion Magnetic Resonance Imaging
Alberto Bizzi et al.
JAMA NEUROLOGY (2020)
Diagnosis of prion diseases by RT-QuIC results in improved surveillance
Daniel D. Rhoads et al.
NEUROLOGY (2020)
MM2-type sporadic Creutzfeldt-Jakob disease: new diagnostic criteria for MM2-cortical type
Tsuyoshi Hamaguchi et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2020)
Creutzfeldt-Jakob disease: a systematic review of global incidence, prevalence, infectivity, and incubation
Lesley Uttley et al.
LANCET INFECTIOUS DISEASES (2019)
RT-QuIC: a new test for sporadic CJD
Alison J. E. Green
PRACTICAL NEUROLOGY (2019)
Imaging and CSF analyses effectively distinguish CJD from its mimics
Peter Rudge et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2018)
Technological advances and changing indications for lumbar puncture in neurological disorders
Joost M. Costerus et al.
LANCET NEUROLOGY (2018)
Validation and utilization of amended diagnostic criteria in Creutzfeldt-Jakob disease surveillance
Peter Hermann et al.
NEUROLOGY (2018)
Acute DWI Reductions In Patients After Single Epileptic Seizures - More Common Than Assumed
Annemarie Huebers et al.
FRONTIERS IN NEUROLOGY (2018)
Doxycycline in early CJD: a double-blinded randomised phase II and observational study
Daniela Varges et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2017)
Insights from Therapeutic Studies for PrP Prion Disease
Kenta Teruya et al.
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE (2017)
Towards an early clinical diagnosis of sporadic CJD VV2 (ataxic type)
Simone Baiardi et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2017)
An autopsy-verified case of steroid-responsive encephalopathy with convulsion and a false-positive result from the real-time quaking-induced conversion assay
Yuichi Hayashi et al.
PRION (2017)
Imaging of Creutzfeldt-Jakob Disease: Imaging Patterns and Their Differential Diagnosis
Diego Cardoso Fragoso et al.
RADIOGRAPHICS (2017)
Characteristics of seizure-induced signal changes on MRI in patients with first seizures
Si Eun Kim et al.
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY (2017)
High diagnostic value of second generation CSF RT-QuIC across the wide spectrum of CJD prions
Alessia Franceschini et al.
SCIENTIFIC REPORTS (2017)
Diagnosis of Human Prion Disease Using Real-Time Quaking-Induced Conversion Testing of Olfactory Mucosa and Cerebrospinal Fluid Samples
Matilde Bongianni et al.
JAMA NEUROLOGY (2017)
Diagnostic and prognostic value of human prion detection in cerebrospinal fluid
Aaron Foutz et al.
ANNALS OF NEUROLOGY (2017)
Cerebrospinal Fluid Real-Time Quaking-Induced Conversion Is a Robust and Reliable Test for Sporadic Creutzfeldt-Jakob Disease: An International Study
Lynne I. McGuire et al.
ANNALS OF NEUROLOGY (2016)
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)
An autopsy-verified case of FTLD-TDP type A with upper motor neuron-predominant motor neuron disease mimicking MM2-thalamic-type sporadic Creutzfeldt-Jakob disease
Yuichi Hayashi et al.
PRION (2016)
Evolution of Diffusion-Weighted Magnetic Resonance Imaging Signal Abnormality in Sporadic Creutzfeldt-Jakob Disease, With Histopathological Correlation
Laura Eisenmenger et al.
JAMA NEUROLOGY (2016)
Characteristic CSF Prion Seeding Efficiency in Humans with Prion Diseases
Maria Cramm et al.
MOLECULAR NEUROBIOLOGY (2015)
Differential Diagnosis of Jakob-Creutzfeldt Disease
Ross W. Paterson et al.
ARCHIVES OF NEUROLOGY (2012)
MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease
Christopher Carswell et al.
BMC NEUROLOGY (2012)
Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future
Piero Parchi et al.
ACTA NEUROPATHOLOGICA (2011)
Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion
Ryuichiro Atarashi et al.
NATURE MEDICINE (2011)
Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias
P. Vitali et al.
NEUROLOGY (2011)
Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification
Piero Parchi et al.
ACTA NEUROPATHOLOGICA (2009)
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease
I. Zerr et al.
BRAIN (2009)
Pathologic correlates of diffusion MRI changes in Creutzfeldt-Jakob disease
D. N. Manners et al.
NEUROLOGY (2009)
MRI lesion profiles in sporadic Creutzfeldt-Jakob disease
B. Meissner et al.
NEUROLOGY (2009)
Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease
S. J. Collins et al.
BRAIN (2006)
Clinical findings and diagnostic tests in the MV2 subtype of sporadic CJD
Anna Krasnianski et al.
BRAIN (2006)
CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease
P. Sanchez-Juan et al.
NEUROLOGY (2006)
Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease
T Hamaguchi et al.
NEUROLOGY (2005)
Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies
M Pocchiari et al.
BRAIN (2004)
分享论文
