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Creutzfeldt Jakobs Disease (CJD)

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Creutzfeldt Jakobs is a rare, degenerative, invariably fatal brain disorder. Typically, onset of symptoms occurs at about age 60. There are three major categories of CJD; Sporatic CJD, Hereditary CJD, and Acquired CJD.

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Sticky: Useful websites by Mike Weins
Started by Mike Weins, 09-07-2014, 04:55 PM
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by ronaldthomas
08-09-2017, 11:55 PM  
Improving Prion Inactivation Validation to Minimize Risks of Iatrogenic Transmission by flatfish
Started by flatfish, 04-13-2021, 10:26 AM
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04-13-2021, 10:26 AM  
Non-white cases of sCJD A 28 year review of United Kingdom National Surveillance Data by flatfish
Started by flatfish, 04-12-2021, 06:01 AM
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04-12-2021, 06:01 AM  
Abnormal prion protein deposits with high seeding activities in the skeletal muscle, by flatfish
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Preclinical transmission of prions by blood transfusion is influenced by... by flatfish
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02-23-2021, 08:02 AM  
hvCJD: First Reported Case from East Africa by flatfish
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Transmission of the atypical/Nor98 scrapie agent to Suffolk sheep with VRQ/ARQ, ... by flatfish
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USA 50 STATE CWD TSE Prion UPDATE FEBRUARY 2021 by flatfish
Started by flatfish, 02-05-2021, 01:41 PM
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02-05-2021, 01:41 PM  
Scrapie TSE Prion United States of America a Review February 2021 Singeltary et al by flatfish
Started by flatfish, 02-05-2021, 12:56 PM
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APHIS Concurrence With OIE Risk Designation for BSE Docket No. APHIS-2018-0087 by flatfish
Started by flatfish, 02-05-2021, 12:54 PM
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Scientists identify locations of early prion protein deposition in retina, what if? by flatfish
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