Results 11 to 20 of about 9,594 (241)

A Contemporary Risk Analysis of Iatrogenic Transmission of Creutzfeldt-Jakob Disease (CJD) via Corneal Transplantation in the United States

Ophthalmology and Therapy, 2020
Background Creutzfeldt-Jakob disease (CJD) is a rare, fatal, neurodegenerative prion disease potentially transmissible through corneal transplantation.
Majid Moshirfar, Yasmyne C Ronquillo, Phillip C Hoopes   +2 more
exaly   +2 more sources

Update on CJD

Res Medica, 2014
In March 1996 the discovery of a new form of Creutzfeldt-Jakob disease (CJD) was announced to a shocked world. In order to understand why this news took the headlines by storm, it is necessary to trace the history of this rare disease and in particular its links with bovine spongiform encephalopathy (BSE), or “mad cow disease”.
Jeanne E. Bell
openalex   +3 more sources

Canadian Creutzfeldt-Jakob disease incidence remained stable during the coronavirus disease (COVID-19) pandemic. [PDF]

Front Neurol
IntroductionHealthcare disruptions imposed by the coronavirus disease (COVID-19) pandemic and possible biological links between SARS-CoV-2 and prion misfolding might influence the prevalence or characteristics of Creutzfeldt-Jakob Disease (CJD).
Slota JA, Todoric D, Bergeron V, Avery K, Phillipson C, Kielich DMS, Myskiw J, Lamoureux L, Frost K, Simon SLR, Bailey-Elkin BA, Booth SA.   +11 more
europepmc   +2 more sources

CJD without borders [PDF]

Nature Reviews Neurology, 2021
José Eriton Gomes da Cunha, Jéssica Catarine Frutuoso do Nascimento, João Ricardo Mendes de Oliveira   +2 more
openalex   +3 more sources

Is there a link between COVID-19 and Creutzfeldt-Jakob Disease? a Case Report [PDF]

Journal of Research in Clinical Medicine, 2021
Creutzfeldt-Jakob Disease (CJD) is a rare rapidly progressive neurodegenerative disease. The diagnosis of CJD is based on magnetic resonance imaging (MRI) findings, electro-encephalography (EEG), or 14-3-3 protein detection.
Ehsan Nasiri, Amirreza Naseri, Mohammad Yazdchi, Mahnaz Talebi   +3 more
doaj   +1 more source

Bleach Usage for CJD Disinfection [PDF]

Infection Control, 1984
Andrea Scheidt
openalex   +3 more sources

Sodium hypochlorite inactivation of human CJD prions

PLoS ONE
Prion diseases are transmissible, fatal neurologic diseases of mammals caused by the accumulation of mis-folded, disease associated prion protein (PrPd).
Bradley R. Groveman, Brent Race, Andrew G. Hughson, Cathryn L. Haigh   +3 more
openalex   +2 more sources

Total and Phosphorylated Cerebrospinal Fluid Tau in the Differential Diagnosis of Sporadic Creutzfeldt-Jakob Disease and Rapidly Progressive Alzheimer’s Disease

Viruses, 2022
Background: CSF total-tau (t-tau) became a standard cerebrospinal fluid biomarker in Alzheimer’s disease (AD). In parallel, extremely elevated levels were observed in Creutzfeldt-Jakob disease (CJD).
Peter Hermann, Philip Haller, Stefan Goebel, Timothy Bunck, Christian Schmidt, Jens Wiltfang, Inga Zerr   +6 more
doaj   +1 more source

Comparative evaluation of clinical and cerebrospinal fluid biomarker characteristics in rapidly and non-rapidly progressive Alzheimer’s disease

Alzheimer’s Research & Therapy, 2023
Background Rapidly progressive forms of Alzheimer’s disease (rpAD) are increasingly recognized and may have a prevalence of up to 30% of patients among all patients with Alzheimer’s disease (AD).
Janne Marieke Herden, Peter Hermann, Isabel Schmidt, Kathrin Dittmar, Sezgi Canaslan, Luise Weglage, Sabine Nuhn, Corinna Volpers, Astrid Schlung, Stefan Goebel, Fabian Kück, Anna Villar-Piqué, Christian Schmidt, Dirk Wedekind, Inga Zerr   +14 more
doaj   +1 more source

CJD transmission [PDF]

Nature, 1997
F. X. Meslin
openalex   +3 more sources