Results 191 to 200 of about 9,594 (241)
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Dental Update, 2003
The last 10 years have seen the emergence of a new disease termed variant CJD. This disease is thought to be initiated by abnormal prion proteins. This article reviews the different clinical manifestations of human prion diseases and provides some background information on the biological nature of this unique infectious agent. Prion proteins present a
Andrew, Smith, Jeremy, Bagg
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The last 10 years have seen the emergence of a new disease termed variant CJD. This disease is thought to be initiated by abnormal prion proteins. This article reviews the different clinical manifestations of human prion diseases and provides some background information on the biological nature of this unique infectious agent. Prion proteins present a
Andrew, Smith, Jeremy, Bagg
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Nursing Management (Springhouse), 2003
Review precautions for the safe handling of surgical materials that may be contaminated with infectious agents from patients with Creutzfeldt-Jakob disease.
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Review precautions for the safe handling of surgical materials that may be contaminated with infectious agents from patients with Creutzfeldt-Jakob disease.
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CNS & Neurological Disorders - Drug Targets, 2009
Creutzfeldt-Jakob disease (CJD) is a rare, degenerative and fatal brain disease that appears to be caused by an abnormal form of a protein called a prion. Due to the lack of an effective treatment for CJD, support for patients and family members is crucial.
Florence J, Kranitz, Deana M, Simpson
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Creutzfeldt-Jakob disease (CJD) is a rare, degenerative and fatal brain disease that appears to be caused by an abnormal form of a protein called a prion. Due to the lack of an effective treatment for CJD, support for patients and family members is crucial.
Florence J, Kranitz, Deana M, Simpson
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Tissue Safety in View of CJD and Variant CJD
Cell and Tissue Banking, 2005Epidemiological studies on human transmissible spongiform encephalopathies (Creutzfeldt-Jakob Disease, CJD) have shown that the agent could be transmitted by highly infectious tissues like brain, spinal cord or retina and medicinal products derived from these tissues (i.e. human growth hormone, dura mater).
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Nursing, 2016
Rare, transmissible, and rapidly progressive, Creutzfeldt-Jakob disease (CJD) is an ultimately fatal central nervous system infection caused by accumulation of abnormally shaped prion proteins in neurons (see Understanding prion proteins). Although categorized as an infection, CJD doesn't lead to the immune system or inflammatory response typical of ...
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Rare, transmissible, and rapidly progressive, Creutzfeldt-Jakob disease (CJD) is an ultimately fatal central nervous system infection caused by accumulation of abnormally shaped prion proteins in neurons (see Understanding prion proteins). Although categorized as an infection, CJD doesn't lead to the immune system or inflammatory response typical of ...
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2003
Abstract Stephen (Steve) Churchill was born on 14 April 1976 in Stockton-on-Tees. He was a second child. His father was a fireman, and the family lived in a large Victorian semidetached house. Steve was a lively child. He played rugby and was a good swimmer.
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Abstract Stephen (Steve) Churchill was born on 14 April 1976 in Stockton-on-Tees. He was a second child. His father was a fireman, and the family lived in a large Victorian semidetached house. Steve was a lively child. He played rugby and was a good swimmer.
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Management of a Cjd Case Part 2 the Patient with Cjd in the Operating Theatre
British Journal of Perioperative Nursing (United Kingdom), 2004Along with details as to how CJD-associated instrumentation should now be handled, following a recent updating of DoH advice, this article contains comprehensive guidelines which can be followed in the event of a procedure involving a CJD patient. All the practicalities associated with managing a CJD case are dealt with step by step, from collection of
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Predicting the CJD epidemic in humans
Nature, 1997Fourteen cases of new-variant Creutzfeldt–Jakob disease have so far been confirmed in the United Kingdom. Are they the start of an epidemic? If so, how informative will cases in the next few years be in predicting its course?
S N, Cousens +4 more
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Dental Update, 2006
It is almost a decade since the recognition of the emergence of a new infectious disease termed variant Creutzfeldt-Jakob disease (vCJD) caused by prions (PrPTSE), abnormal variants of a normal human cell surface protein (PrP). This disease has a number of similarities to other forms of CJD - lethal disorders characterized by a prolonged incubation ...
Crispian, Scully +2 more
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It is almost a decade since the recognition of the emergence of a new infectious disease termed variant Creutzfeldt-Jakob disease (vCJD) caused by prions (PrPTSE), abnormal variants of a normal human cell surface protein (PrP). This disease has a number of similarities to other forms of CJD - lethal disorders characterized by a prolonged incubation ...
Crispian, Scully +2 more
openaire +2 more sources