[Acquired human prion diseases--past and present issues].

No abstract is available for this paper.

• Publication year

  2009

• Venue

  Uirusu

• Publication date

  2009-12-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.2222/jsv.59.155PMID 20218324
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Research Letters

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• New hospital disinfection processes for both conventional and prion infectious agents compatible with thermosensitive medical equipment.

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• Ultraviolet-ozone treatment reduces levels of disease-associated prion protein and prion infectivity

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• Synthetic fibril peptide promotes clearance of scrapie prion protein by lysosomal degradation

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• Human platelets as a substrate source for the in vitro amplification of the abnormal prion protein (PrPSc) associated with variant Creutzfeldt‐Jakob disease

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• Simplified ultrasensitive prion detection by recombinant PrP conversion with shaking

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• The origin of the prion agent of kuru: molecular and biological strain typing

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• Atypical BSE (BASE) Transmitted from Asymptomatic Aging Cattle to a Primate

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• A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea

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• Progression of prion infectivity in asymptomatic cattle after oral bovine spongiform encephalopathy challenge.

  2007cited by this paper
• Prevention of prion propagation by dehydrocholesterol reductase inhibitors in cultured cells and a therapeutic trial in mice.

  2007cited by this paper
• Prion inactivation using a new gaseous hydrogen peroxide sterilisation process.

  2007cited by this paper
• Prion inactivation by the Maillard reaction.

  2007cited by this paper
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  2006cited by this paper
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• Presymptomatic Detection of Prions in Blood

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  2006cited by this paper
• A third episode of transfusion-derived vCJD.

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• Healthcare Epidemiology: Methods to Minimize the Risks of Creutzfeldt‐Jakob Disease Transmission by Surgical Procedures: Where to Set the Standard?

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• Highly bovine spongiform encephalopathy-sensitive transgenic mice confirm the essential restriction of infectivity to the nervous system in clinically diseased cattle.

  2005cited by this paper
• In vitro generation of infectious scrapie prions.

  2005cited by this paper
• Detection of prions in blood

  2005cited by this paper
• Experiments on maternal and paternal transmission of Creutzfeldt-Jakob disease in mice

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• Pre‐symptomatic detection of prions by cyclic amplification of protein misfolding

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• Distinct molecular phenotypes in bovine prion diseases

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• Squalestatin Cures Prion-infected Neurons and Protects Against Prion Neurotoxicity*

  2004cited by this paper
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  2004cited by this paper
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• Polymorphisms of the Prion Protein gene in italian patients with Creutzfeldt-Jakob disease

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• Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion.

  2004cited by this paper
• Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient.

  2004cited by this paper
• Oral prion infection requires normal numbers of Peyer's patches but not of enteric lymphocytes.

  2003cited by this paper
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  2003cited by this paper
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  2003cited by this paper
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  2002cited by this paper
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  2002cited by this paper
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  2001cited by this paper
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  2001cited by this paper
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  2001cited by this paper
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  2001cited by this paper
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  2000cited by this paper
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  2000cited by this paper
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  2000cited by this paper
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  1999cited by this paper
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  1999cited by this paper
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  1999cited by this paper
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  1998cited by this paper
• Phenotype-genotype studies in kuru: implications for new variant Creutzfeldt-Jakob disease.

  1998cited by this paper
• Prion immunoreactivity in appendix before clinical onset of variant Creutzfeldt-Jakob disease.

  1998cited by this paper
• Transmission dynamics and epidemiology of BSE in British cattle

  1997cited by this paper
• Transmissions to mice indicate that ‘new variant’ CJD is caused by the BSE agent

  1997cited by this paper
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  1997cited by this paper
• Prion diseases of humans and animals

  1996cited by this paper
• Transmission dynamics and epidemiology of BSE in British cattle

  1996cited by this paper
• Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD

  1996cited by this paper
• A new variant of Creutzfeldt-Jakob disease in the UK.

  1996cited by this paper
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  1995cited by this paper
• Creutzfeldt-Jakob disease and blood transfusion.

  1994cited by this paper
• Molecular genetics of prion diseases in France

  1994cited by this paper
• Synthesis and trafficking of prion proteins in cultured cells.

  1992cited by this paper
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  1987cited by this paper
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