Mad Cow Disease and Related Spongiform Encephalopathies:
Bovine spongiform encephalopathy (BSE) has become the most publicly recognizable example of a group of fatal neurodegenerative diseases caused by proteinaceous infectious particles called prions. Transmission of bovine spongiform encephalopathy to humans in the form of variant Creutzfeldt-Jakob dise...
Gespeichert in:
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| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
Berlin, Heidelberg
Springer Berlin Heidelberg
2004
|
| Schriftenreihe: | Current Topics in Microbiology and Immunology
284 |
| Schlagworte: | |
| Online-Zugang: | UBR01 URL des Erstveröffentlichers |
| Zusammenfassung: | Bovine spongiform encephalopathy (BSE) has become the most publicly recognizable example of a group of fatal neurodegenerative diseases caused by proteinaceous infectious particles called prions. Transmission of bovine spongiform encephalopathy to humans in the form of variant Creutzfeldt-Jakob disease (vCJD) has intensified the urgency of understanding and controlling these unusual disorders. The contributors to this volume, all internationally recognized experts in their fields, provide an introduction to prion biology, followed by reviews of the latest information on BSE, vCJD, and chronic wasting disease, an animal prion disease that has recently emerged in North America |
| Beschreibung: | 1 Online-Ressource (VII, 222 p) |
| ISBN: | 9783662084410 |
| DOI: | 10.1007/978-3-662-08441-0 |
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| spelling | Mad Cow Disease and Related Spongiform Encephalopathies edited by David A. Harris Berlin, Heidelberg Springer Berlin Heidelberg 2004 1 Online-Ressource (VII, 222 p) txt rdacontent c rdamedia cr rdacarrier Current Topics in Microbiology and Immunology 284 Bovine spongiform encephalopathy (BSE) has become the most publicly recognizable example of a group of fatal neurodegenerative diseases caused by proteinaceous infectious particles called prions. Transmission of bovine spongiform encephalopathy to humans in the form of variant Creutzfeldt-Jakob disease (vCJD) has intensified the urgency of understanding and controlling these unusual disorders. The contributors to this volume, all internationally recognized experts in their fields, provide an introduction to prion biology, followed by reviews of the latest information on BSE, vCJD, and chronic wasting disease, an animal prion disease that has recently emerged in North America Neurosciences Transmissible spongiform Encephalopathies (DE-588)4747411-7 gnd rswk-swf BSE (DE-588)4345150-0 gnd rswk-swf (DE-588)4143413-4 Aufsatzsammlung gnd-content BSE (DE-588)4345150-0 s DE-604 Transmissible spongiform Encephalopathies (DE-588)4747411-7 s Harris, David A. edt Erscheint auch als Druck-Ausgabe 9783642057564 Erscheint auch als Druck-Ausgabe 9783540201076 Erscheint auch als Druck-Ausgabe 9783662084427 https://doi.org/10.1007/978-3-662-08441-0 Verlag URL des Erstveröffentlichers Volltext |
| spellingShingle | Mad Cow Disease and Related Spongiform Encephalopathies Neurosciences Transmissible spongiform Encephalopathies (DE-588)4747411-7 gnd BSE (DE-588)4345150-0 gnd |
| subject_GND | (DE-588)4747411-7 (DE-588)4345150-0 (DE-588)4143413-4 |
| title | Mad Cow Disease and Related Spongiform Encephalopathies |
| title_auth | Mad Cow Disease and Related Spongiform Encephalopathies |
| title_exact_search | Mad Cow Disease and Related Spongiform Encephalopathies |
| title_full | Mad Cow Disease and Related Spongiform Encephalopathies edited by David A. Harris |
| title_fullStr | Mad Cow Disease and Related Spongiform Encephalopathies edited by David A. Harris |
| title_full_unstemmed | Mad Cow Disease and Related Spongiform Encephalopathies edited by David A. Harris |
| title_short | Mad Cow Disease and Related Spongiform Encephalopathies |
| title_sort | mad cow disease and related spongiform encephalopathies |
| topic | Neurosciences Transmissible spongiform Encephalopathies (DE-588)4747411-7 gnd BSE (DE-588)4345150-0 gnd |
| topic_facet | Neurosciences Transmissible spongiform Encephalopathies BSE Aufsatzsammlung |
| url | https://doi.org/10.1007/978-3-662-08441-0 |
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