Prion Diseases
In Prion Diseases leading researchers and clinicians describe their state-of-the-art findings and hypotheses arising from a variety of different approaches to this group of diseases. Their approaches include clinical presentations, epidemiology, transgenic methods, and diagnostic tests via transmiss...
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| Other Authors: | , |
| Format: | Electronic eBook |
| Language: | English |
| Published: |
Totowa, NJ :
Humana Press : Imprint: Humana,
1996.
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| Edition: | 1st ed. 1996. |
| Series: | Methods in Molecular Medicine,
3 |
| Subjects: | |
| Online Access: | https://doi.org/10.1385/0896033422 |
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Table of Contents:
- The Paradox of Prion Disease
- Human Spongiform Encephalopathy
- Neuropathological Diagnosis of Human Prion Disease
- Neuropathological Diagnosis of Human Prion Disease
- The Diagnosis of Bovine Spongiform Encephalopathy and Scrapie by the Detection of Fibrils and the Abnormal Protein lsoform
- Exposure to, and Inactivation of, the Unconventional Agents that Cause Transmissible Degenerative Encephalopathies
- Surveillance of Prion Diseases in Humans
- Environmental Causes of Human Spongiform Encephalopathy
- Bovine Spongiform Encephalopathy
- Handling the BSE Epidemic in Great Britain
- Special Problems of Genetic Counseling in Adult-Onset Diseases
- Genotyping and Susceptibility of Sheep to Scrapie
- Strain Typing Studies of Scrapie and BSE
- PrP-Deficient Mice in the Study of Transmissible Spongiform Encephalopathies
- Transgenic Approaches to Prion “Species-Barrier” Effects
- Methods for Studying Prion Protein Amyloid
- Methods for Studying Prion Protein (PrP) Metabolism and the Formation of Protease-Resistant PrP in Cell Culture and Cell-Free Systems
- Immunohistochemistry of Resinated Tissues for Light and Electron Microscopy.