Results 111 to 120 of about 35,863 (248)

Efficient transmission and characterization of creutzfeldt-jakob disease strains in bank voles.

open access: yesPLoS Pathogens, 2006
Transmission of prions between species is limited by the "species barrier," which hampers a full characterization of human prion strains in the mouse model.
Romolo Nonno   +14 more
doaj   +2 more sources

The molecular epidemiology of variant CJD [PDF]

open access: yes, 2011
The emergence of the novel prion diseases bovine spongiform encephalopathy (BSE) and, subsequently, variant Creutzfeldt-Jakob disease (vCJD) in epidemic forms has attracted much scientific attention.
Ironside, James W   +2 more
core   +1 more source

Dura mater-associated Creutzfeldt-Jakob disease:experience from surveillance in the UK [PDF]

open access: yes, 2006
Between 1970 and 2003, seven cases of human dura mater‐associated Creutzfeldt–Jakob disease (CJD) were identified in the UK. Furthermore, we identified a case of CJD in a porcine dura graft recipient.
Barker, R A   +11 more
core   +2 more sources

Acute ascending polyradiculoneuritis in a case of Creutzfeldt-Jakob disease. [PDF]

open access: bronze, 1977
Enrique Såenz Lope   +3 more
openalex   +1 more source

Sporadic Creutzfeldt–Jakob disease

open access: yes, 2018
Sporadic Creutzfeldt-Jakob disease (CJD), the most common human prion disease, is generally regarded as a spontaneous neurodegenerative illness, arising either from a spontaneous PRNP somatic mutation or a stochastic PrP structural change. Alternatively, the possibility of an infection from animals or other source remains to be completely ruled out ...
Zerr, Inga, Parchi, Piero
openaire   +4 more sources

A Case of sporadic Creutzfeldt-Jakob disease [PDF]

open access: diamond, 2023
Fatma Şimşek, Recep Yevgi
openalex   +1 more source

Does Improvement in Case Ascertainment Explain the Increase in Sporadic Creutzfeldt-Jakob Disease Since 1970 in the United Kingdom? [PDF]

open access: yes, 2017
The aim of this study was to quantify the improvements in case ascertainment which are considered to explain the rise in the incidence of sporadic Creutzfeldt-Jakob disease.
Cohen, Carine H.
core  

Clinical perspectives of emerging pathogens in bleeding disorders. [PDF]

open access: yes, 2006
As a result of immunological and nucleic-acid screening of plasma donations for transfusion-transmissible viruses, and the incorporation of viral reduction processes during plasma fractionation, coagulation-factor concentrates (CFC) are now judged safe ...
Bozzette, Samuel   +11 more
core   +1 more source

Complicated symptomatology and diagnosis of Creuzfeld-Jakob disease on a basis of clinical case

open access: yesQuality in Sport
Creutzfeldt-Jakob disease (CJD) is a rare condition. In this study we describe the diagnosis of the disease in a 73-year old female, presenting dementia. Diagnostic tests unveiled characteristic features of CJD. The diagnosis of CJD was confirmed. It is
Marta Jurga   +9 more
doaj   +1 more source

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