Validation of Revised International Creutzfeldt-Jakob Disease Surveillance Network Diagnostic Criteria for Sporadic Creutzfeldt-Jakob Disease
Sign Up to like & getrecommendations! Published in 2022 at "JAMA Network Open"
DOI: 10.1001/jamanetworkopen.2021.46319
Abstract: Key Points Question How sensitive and specific are the 2017 revised International Creutzfeldt-Jakob disease Surveillance Network diagnostic criteria for the diagnosis of sporadic Creutzfeldt-Jakob disease? Findings In this diagnostic study of 647 individuals conducted by… read more here.
Keywords: creutzfeldt jakob; jakob disease; diagnostic criteria;
Prevention of Creutzfeldt-Jakob Disease in Patients Undergoing Surgery.
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DOI: 10.1001/jamanetworkopen.2022.1561
Abstract: assess the potential for iatrogenic transmission of the rare but devastating Creutzfeldt-Jakob disease (CJD) through surgical procedures prior to CJD diagnosis. The authors performed a retrospective analysis of 121 patients with probable or definite CJD… read more here.
Keywords: creutzfeldt jakob; jakob disease; prevention creutzfeldt;
Analysis of Clinical Features, Diagnostic Tests, and Biomarkers in Patients With Suspected Creutzfeldt-Jakob Disease, 2014-2021
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DOI: 10.1001/jamanetworkopen.2022.25098
Abstract: Key Points Question What is the diagnostic utility associated with clinical features and tests historically associated with Creutzfeldt-Jakob disease (CJD) in patients evaluated in the modern era? Findings In this cohort study including 115 patients,… read more here.
Keywords: creutzfeldt jakob; jakob disease; patients suspected; clinical features ... See more keywords
Accumulation of prion protein in the vagus nerve in creutzfeldt–jakob disease
Sign Up to like & getrecommendations! Published in 2019 at "Annals of Neurology"
DOI: 10.1002/ana.25451
Abstract: Disease‐associated proteins are thought to propagate along neuronal processes in neurodegenerative diseases. To detect disease‐associated prion protein (PrPSc) in the vagus nerve in different forms and molecular subtypes of Creutzfeldt–Jakob disease (CJD), we applied 3… read more here.
Keywords: cjd; disease; jakob disease; vagus nerve ... See more keywords
Default Mode Network quantitative diffusion and resting‐state functional magnetic resonance imaging correlates in sporadic Creutzfeldt‐Jakob disease
Sign Up to like & getrecommendations! Published in 2022 at "Human Brain Mapping"
DOI: 10.1002/hbm.25945
Abstract: Grey matter involvement is a well‐known feature in sporadic Creutzfeldt–Jakob disease (sCJD), yet precise anatomy‐based quantification of reduced diffusivity is still not fully understood. Default Mode Network (DMN) areas have been recently demonstrated as selectively… read more here.
Keywords: disease; creutzfeldt jakob; sporadic creutzfeldt; diffusivity ... See more keywords
Creutzfeldt–Jakob Disease Misdiagnosed as Multiple System Atrophy
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DOI: 10.1002/mdc3.13654
Abstract: Multiple system atrophy (MSA) is a progressive neurodegenerative disorder characterized by various combinations of autonomic failure, parkinsonism, and cerebellar syndromes. Although consensus criteria have been widely used to diagnose MSA, accurate clinical diagnosis remains challenging.… read more here.
Keywords: creutzfeldt jakob; jakob disease; multiple system; system atrophy ... See more keywords
Diagnostic value of surrogate CSF biomarkers for Creutzfeldt–Jakob disease in the era of RT-QuIC
Sign Up to like & getrecommendations! Published in 2019 at "Journal of Neurology"
DOI: 10.1007/s00415-019-09537-0
Abstract: Prion real-time quaking-induced conversion (RT-QuIC) is emerging as the most potent assay for the in vivo diagnosis of Creutzfeldt–Jakob disease (CJD), but its full application, especially as a screening test, is limited by suboptimal substrate… read more here.
Keywords: diagnosis; surrogate; csf; jakob disease ... See more keywords
Atypical presentation of probable Creutzfeldt-Jakob disease associated with anti-Zic4 antibody: Literature review of neuronal antibodies in Creutzfeldt-Jakob disease
Sign Up to like & getrecommendations! Published in 2018 at "Clinical Neurology and Neurosurgery"
DOI: 10.1016/j.clineuro.2018.02.043
Abstract: INTRODUCTION Sporadic Creutzfeldt-Jakob disease is a prion disease characterized by rapidly progressive dementia, ataxia and myoclonus. Atypical phenotype masquerading as stroke, movement disorders or autoimmune encephalitis have been described. Here, I report a probable case… read more here.
Keywords: anti zic4; disease; jakob disease; neuronal antibodies ... See more keywords
Diffusion-weighted imaging negative M232R familial Creutzfeldt-Jakob disease
Sign Up to like & getrecommendations! Published in 2019 at "Journal of Clinical Neuroscience"
DOI: 10.1016/j.jocn.2019.03.019
Abstract: The familial Creutzfeldt-Jakob disease (fCJD) usually has similar clinical and neuroimaging features as sporadic CJD (sCJD). A 57-year-old man presented with a four-month history of rapidly progressive dementia (RPD). Laboratory tests for RPD were all… read more here.
Keywords: familial creutzfeldt; weighted imaging; jakob disease; diffusion weighted ... See more keywords
How common are seizures in the heidenhain variant of creutzfeldt-jakob disease? A case report and systematic review
Sign Up to like & getrecommendations! Published in 2021 at "Journal of Clinical Neuroscience"
DOI: 10.1016/j.jocn.2020.10.002
Abstract: The Heidenhain variant of Creutzfeld-Jakob disease (HvCJD) is a relentlessly progressive and fatal neurodegenerative disorder characterised by prominent visual features early in its clinical course. However, seizures are uncommonly reported in HvCJD. The case history… read more here.
Keywords: systematic review; jakob disease; heidenhain variant; review ... See more keywords
Atypical and early symptoms of sporadic Creutzfeldt – Jakob disease: case series and review of the literature
Sign Up to like & getrecommendations! Published in 2020 at "International Journal of Neuroscience"
DOI: 10.1080/00207454.2020.1759594
Abstract: Abstract Background Prion diseases are rapidly progressive fatal conditions caused by abnormally shaped proteins. Sporadic Creutzfeldt - Jakob disease (sCJD) is the most common human prion disorder accounting for 85–90 % of cases. Clinical manifestations… read more here.
Keywords: early symptoms; sporadic creutzfeldt; disease; jakob disease ... See more keywords