The article discusses the current views on the causes of various types of slow infections and their main features that are encountered in the practice of forensic experts and features of forensic examination. The urgency of the study of prion diseases is due to the fact that they are pathogens extremely dangerous for human and animal infections. Such diseases are diagnosed in all countries of the world, and the agents of scrapie and rabies cows from the UK have been imported to a number of countries in Europe, the Middle East and Asia. Modern quarantine measures to eliminate epizootic are time consuming, cause huge economic damage to the state, and also have a negative impact on the social situation. Domestic and foreign scientists have res...
Prion diseases which are serious neurodegenerative diseases that affect humans and animals occur in ...
While rare in humans, the prion diseases have become an area of intense clinical and scientific inte...
Copyright © 2012 Peter Hedlin et al. This is an open access article distributed under the Creative C...
Prion diseases (or transmissible spongiform encephalopathies) are rare, infectious neurodegenerative...
Human prion disorders (transmissible spongiform encephalopathies, TSEs) are unique, progressive, and...
A prion is a small infectious particle, which resist inactivation by procedures that modify nucleic ...
Prion diseases are unique group of neurodegenerative diseases including the transmissible spongiform...
Prion diseases or transmissible spongiform encephalopathies are a group of closely related transmiss...
Prion diseases or transmissible spongiform encephalopathies (TSEs) are rare, fatal and incurable neu...
Prion diseases, or transmissible spongiform encephalopathies (TSE), are a group of neurodegenerative...
Purpose of reviewThis article presents an update on the clinical aspects of human prion disease, inc...
Prion diseases are caused by a misfolded protein which have the uncanny ability to escape destructio...
Prion diseases, or transmissible spongiform encephalopathies (TSEs), are a group of fatal and transm...
AbstractTransmissible spongiform encephalopathy (TSE) agents or prions induce neurodegenerative fata...
Prion diseases are a group of diseases caused by abnormally conformed infectious proteins, called pr...
Prion diseases which are serious neurodegenerative diseases that affect humans and animals occur in ...
While rare in humans, the prion diseases have become an area of intense clinical and scientific inte...
Copyright © 2012 Peter Hedlin et al. This is an open access article distributed under the Creative C...
Prion diseases (or transmissible spongiform encephalopathies) are rare, infectious neurodegenerative...
Human prion disorders (transmissible spongiform encephalopathies, TSEs) are unique, progressive, and...
A prion is a small infectious particle, which resist inactivation by procedures that modify nucleic ...
Prion diseases are unique group of neurodegenerative diseases including the transmissible spongiform...
Prion diseases or transmissible spongiform encephalopathies are a group of closely related transmiss...
Prion diseases or transmissible spongiform encephalopathies (TSEs) are rare, fatal and incurable neu...
Prion diseases, or transmissible spongiform encephalopathies (TSE), are a group of neurodegenerative...
Purpose of reviewThis article presents an update on the clinical aspects of human prion disease, inc...
Prion diseases are caused by a misfolded protein which have the uncanny ability to escape destructio...
Prion diseases, or transmissible spongiform encephalopathies (TSEs), are a group of fatal and transm...
AbstractTransmissible spongiform encephalopathy (TSE) agents or prions induce neurodegenerative fata...
Prion diseases are a group of diseases caused by abnormally conformed infectious proteins, called pr...
Prion diseases which are serious neurodegenerative diseases that affect humans and animals occur in ...
While rare in humans, the prion diseases have become an area of intense clinical and scientific inte...
Copyright © 2012 Peter Hedlin et al. This is an open access article distributed under the Creative C...