4.5 Review

Variant CJD: Reflections a Quarter of a Century on

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。
Article Clinical Neurology

Wide distribution of prion infectivity in the peripheral tissues of vCJD and sCJD patients

Jean-Yves Douet et al.

Summary: Sporadic Creutzfeldt-Jakob disease (sCJD) typically occurs in the central nervous system, but recent research has shown prion infectivity detected in peripheral tissues of patients as well. Although infectivity levels varied unpredictably among different patients and tissues, these findings may alter our perception of transmission risks associated with sCJD.

ACTA NEUROPATHOLOGICA (2021)

Review Clinical Neurology

The importance of ongoing international surveillance for Creutzfeldt-Jakob disease

Neil Watson et al.

Summary: Despite the decreasing incidence of variant Creutzfeldt-Jakob disease, evidence suggests that patients with different forms of human prion diseases still carry a theoretical risk of transmission, highlighting the continued importance of monitoring for Creutzfeldt-Jakob disease.

NATURE REVIEWS NEUROLOGY (2021)

Letter Medicine, General & Internal

Variant Creutzfeldt-Jakob Disease Diagnosed 7.5 Years after Occupational Exposure

Jean-Philippe Brandel et al.

NEW ENGLAND JOURNAL OF MEDICINE (2020)

Article Immunology

No Adaptation of the Prion Strain in a Heterozygous Case of Variant Creutzfeldt-Jakob Disease

Aileen Boyle et al.

EMERGING INFECTIOUS DISEASES (2020)

Article Multidisciplinary Sciences

The emergence of classical BSE from atypical/Nor98 scrapie

Alvina Huor et al.

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

Article Clinical Neurology

RT-QuIC: a new test for sporadic CJD

Alison J. E. Green

PRACTICAL NEUROLOGY (2019)

Article Pathology

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

Marcelo A. Barria et al.

JOURNAL OF PATHOLOGY CLINICAL RESEARCH (2018)

Letter Medicine, General & Internal

Variant Creutzfeldt-Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129

Tzehow Mok et al.

NEW ENGLAND JOURNAL OF MEDICINE (2017)

Article Neurosciences

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

Matthias Schmitz et al.

MOLECULAR NEUROBIOLOGY (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 Pathology

Hospital autopsy: Endangered or extinct?

Angus Turnbull et al.

JOURNAL OF CLINICAL PATHOLOGY (2015)

Letter Clinical Neurology

Variant Creutzfeldt-Jakob disease in older patients

Salwa el Tawil et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2015)

Article Immunology

Recent US Case of Variant Creutzfeldt-Jakob Disease-Global Implications

Atul Maheshwari et al.

EMERGING INFECTIOUS DISEASES (2015)

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 Microbiology

Preclinical Detection of Variant CJD and BSE Prions in Blood

Caroline Lacroux et al.

PLOS PATHOGENS (2014)

Editorial Material Hematology

The French surveillance network of Creutzfeldt-Jakob disease. Epidemiological data in France and worldwide

J-P Brandel et al.

TRANSFUSION CLINIQUE ET BIOLOGIQUE (2013)

Article Biotechnology & Applied Microbiology

Sensitive and specific detection of sporadic Creutzfeldt-Jakob disease brain prion protein using real-time quaking-induced conversion

Alexander H. Peden et al.

JOURNAL OF GENERAL VIROLOGY (2012)

Letter Clinical Neurology

Variant Creutzfeldt-Jakob disease occurring in mother and son

Mario Riverol et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2012)

Article Immunology

Constant Transmission Properties of Variant Creutzfeldt-Jakob Disease in 5 Countries

Abigail B. Diack et al.

EMERGING INFECTIOUS DISEASES (2012)

Article Immunology

latrogenic Creutzfeldt-Jakob Disease, Final Assessment

Paul Brown et al.

EMERGING INFECTIOUS DISEASES (2012)

Article Medicine, General & Internal

Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay

Julie Ann Edgeworth et al.

LANCET (2011)

Article Biochemistry & Molecular Biology

Real-time quaking-induced conversion A highly sensitive assay for prion detection

Ryuichiro Atarashi et al.

Article Clinical Neurology

Variant Creutzfeldt-Jakob disease: the first confirmed case from Portugal shows early onset, long duration and unusual pathology

C. Barbot et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2010)

Article Multidisciplinary Sciences

Human Prion Diseases in the United States

Robert C. Holman et al.

PLOS ONE (2010)

Article Multidisciplinary Sciences

Uncertainty in the Tail of the Variant Creutzfeldt-Jakob Disease Epidemic in the UK

Tini Garske et al.

PLOS ONE (2010)

Article Clinical Neurology

Probable variant Creutzfeldt-Jakob disease in Asia: A case report from Taiwan and review of two prior cases

Chih-Wen Yang et al.

PSYCHIATRY AND CLINICAL NEUROSCIENCES (2010)

Article Clinical Neurology

Variant Creutzfeldt-Jakob Disease in France and the United Kingdom: Evidence for the Same Agent Strain

Jean-Philippe Brandel et al.

ANNALS OF NEUROLOGY (2009)

Editorial Material Medicine, General & Internal

Variant CJD in an individual heterozygous for PRNP codon 129

Diego Kaski et al.

LANCET (2009)

Article Multidisciplinary Sciences

No Major Change in vCJD Agent Strain after Secondary Transmission via Blood Transfusion

Matthew T. Bishop et al.

PLOS ONE (2008)

Article Immunology

Source of variant Creutzfeldt-Jakob disease outside United Kingdom

Pascual Sanchez-Juan et al.

EMERGING INFECTIOUS DISEASES (2007)

Article Biotechnology & Applied Microbiology

Abnormal prion protein in the pituitary in sporadic and variant Creutzfeldt-Jakob disease

Alexander H. Peden et al.

JOURNAL OF GENERAL VIROLOGY (2007)

Article Microbiology

Conversion of the BASE prion strain into the BSE strain: The origin of BSE?

Raffaella Capobianco et al.

PLOS PATHOGENS (2007)

Article Multidisciplinary Sciences

Dissociation of pathological and molecular phenotype of variant Creutzfeldt-Jakob disease in transgenic human prion protein 129 heterozygous mice

Emmanuel A. Asante et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)

Article Clinical Neurology

Risk factors for variant Creutzfeldt-Jakob disease: A case-control study

HJT Ward et al.

ANNALS OF NEUROLOGY (2006)

Article Medicine, General & Internal

Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion

CA Llewelyn et al.

LANCET (2004)

Article Infectious Diseases

Epidemiological evidence of higher susceptibility to vCJD in the young -: art. no. 26

PY Boëlle et al.

BMC INFECTIOUS DISEASES (2004)

Article Multidisciplinary Sciences

Human prion protein with valine 129 prevents expression of variant CJD phenotype

JDF Wadsworth et al.

SCIENCE (2004)

Article Clinical Neurology

Diagnostic value of periodic complexes in Creutzfeldt-Jakob disease

BJ Steinhoff et al.

ANNALS OF NEUROLOGY (2004)

Review Multidisciplinary Sciences

Protein folding and misfolding

CM Dobson

NATURE (2003)

Article Biochemistry & Molecular Biology

The sympathetic nervous system is involved in variant Creutzfeldt-Jakob disease

S Haïk et al.

NATURE MEDICINE (2003)

Article Health Care Sciences & Services

Mortality trend from sporadic Creutzfeldt-Jakob disease (CJD) in Italy, 1993-2000

M Puopolo et al.

JOURNAL OF CLINICAL EPIDEMIOLOGY (2003)

Review Health Care Sciences & Services

Short-term projections for variant Creutzfeldt-Jakob disease onsets

AC Ghani et al.

STATISTICAL METHODS IN MEDICAL RESEARCH (2003)

Article Medicine, General & Internal

Bovine spongiform encephalopathy (BSE) and its epidemiology

PG Smith et al.

BRITISH MEDICAL BULLETIN (2003)

Letter Clinical Neurology

Irregular presence of abnormal prion protein in appendix in variant Creutzfeldt-Jakob disease

S Joiner et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2002)

Article Biotechnology & Applied Microbiology

Transmission of prion diseases by blood transfusion

N Hunter et al.

JOURNAL OF GENERAL VIROLOGY (2002)

Article Clinical Neurology

Sensory features of variant Creutzfeldt-Jakob disease

MA Macleod et al.

JOURNAL OF NEUROLOGY (2002)

Article Clinical Neurology

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)

Article Medicine, General & Internal

Transmission of BSE by blood transfusion in sheep

F Houston et al.

LANCET (2000)