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Books on the topic 'Prion diseases'

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Author: Grafiati

Published: 4 June 2021

Last updated: 28 July 2024

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1

1942-, Prusiner Stanley B., and Ridley Rosalind M, eds. Prion biology and diseases. Cold Spring Harbor, New York: Cold Spring Harbor Laboratory Press, 1999.

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2

Baker, Harry F., and Rosalind M. Ridley. Prion Diseases. New Jersey: Humana Press, 1996. http://dx.doi.org/10.1385/0896033422.

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3

Groschup, Martin H., and Hans A. Kretzschmar, eds. Prion Diseases. Vienna: Springer Vienna, 2000. http://dx.doi.org/10.1007/978-3-7091-6308-5.

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4

Liberski, Pawel P., ed. Prion Diseases. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7211-1.

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5

F, Baker Harry, and Ridley Rosalind M, eds. Prion diseases. Totowa, N.J: Humana Press, 1996.

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6

MD, Collinge John, and Palmer Mark S, eds. Prion diseases. Oxford: Oxford University Press, 1997.

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7

C, Telling Glenn, ed. Prions and prion diseases: Current perspectives. Norfolk, Eng: Horizon Bioscience, 2004.

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8

O, Morrison Douglas R., North Atlantic Treaty Organization. Scientific Affairs Division., and NATO Advanced Research Workshop on Prions and Brain Diseases in Animals and Humans (1996 : Erice, Italy), eds. Prions and brain diseases in animals and humans. New York: Plenum Press, in cooperation with NATO Scientific Affairs Division, 1998.

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9

Prion biology: Research and advances. Toronto: Apple Academic Press, 2013.

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10

F, Baker Harry, ed. Molecular and cellular pathology in prion disease. Totowa, N.J: Humana Press, 2001.

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11

Zou, Wen-Quan, and Pierluigi Gambetti. Prions and diseases. New York: Springer, 2013.

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12

PhD, Brown David R., ed. Neurodegeneration and prion disease. New York, NY: Springer Science+Business Media, 2005.

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13

1965-, Lehmann Sylvain, and Grassi Jacques 1951-, eds. Techniques in prion research. Basel: Birkhäuser, 2004.

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14

1942-, Prusiner Stanley B., ed. Prion diseases of humans and animals. New York: Ellis Horwood, 1992.

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15

Schwartz, Maxime. How the cows turned mad: Unlocking the mysteries of mad cow disease. Berkeley: University of California Press, 2004.

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16

Fatal flaws: How a misfolded protein baffled scientists and changed the way we look at the brain. Toronto, Ont: HarperCollins, 2012.

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17

Science, Institute of Medicine (U S. ). Committee on Transmissible Spongiform Encephalopathies: Assessment of Relevant. Advancing prion science: Guidance for the national prion research program. Washington, D.C: National Academies Press, 2004.

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18

Dr, Soto Claudio, ed. Prions: The new biology of proteins. Boca Raton, FL: CRC/Taylor & Francis, 2006.

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19

I, Lasmezas C., Adams D. B, and International Office of Epizootics, eds. Risk analysis of prion diseases in animals. Paris: Office International des Épizooties, 2003.

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20

Beauvais, Pierre. Maladie de Creutzfeldt-Jakob et autres maladies à prion. Paris: Flammarion médicine-sciences, 1996.

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21

Liberski, P. P. The enigma of slow viruses: Facts and artefacts. Wien: Springer-Verlag, 1993.

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22

Rick, Erdtmann, Sivitz Laura, and Institute of Medicine (U.S.). Committee on Transmissible Spongiform Encephalopathies: Assessment of Relevant Science., eds. Advancing prion science: Guidance for the National Prion Research Program, interim report. Washington, D.C: National Academies Press, 2003.

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23

Mastrianni, James A., and Joshuae G. Gallardo. Prion Diseases. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0166.

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Prion diseases are transmissible fatal neurodegenerative disorders resulting from the accumulation of misfolded prion protein. Although primarily sporadic diseases, 5% to 10% result from a mutation of the prion protein gene (PRNP), and less than 1% occur from exposure to prions. The current family of prion diseases includes Creutzfeldt-Jakob disease (CJD), Gerstmann-Sträussler-Scheinker disease (GSS), fatal insomnia (FI), variant CJD (vCJD), and variably protease-sensitive prionopathy (VPSPr). Kuru is a disease of historical interest that was transmitted through cannibalistic rituals. Iatrogenic CJD (iCJD) is the result of secondary transmission of prion disease from contaminated biologicals.

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24

1942-, Prusiner Stanley B., ed. Prion biology and diseases. 2nd ed. Cold Spring Harbor, N.Y: Cold Spring Harbor Laboratory Press, 2004.

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25

Prusiner, Stanley B. Prion Biology and Diseases. Cold Spring Harbor Laboratory Press, 1999.

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26

Prion Diseases. Cold Spring Harbor Laboratory Press, 2017.

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27

Prusiner, Stanley B. Prion Diseases. Oxford University Press, 2017.

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28

Ridley, Rosalind M., and Harry F. Baker. Prion Diseases. Humana Press, 2013.

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29

Liberski, Pawel. Prion Diseases. Humana Press, 2017.

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30

Liberski, Pawel P. Prion Diseases. Springer New York, 2018.

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31

Cashman, Neil. Prions and Prion Diseases (Neurological Disease and Therapy). Informa Healthcare, 2009.

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32

Verdier, Jean-Michel. Prions and Prion Diseases: New Developments. Nova Science Publishers, Incorporated, 2012.

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33

Manson, Jean, and Maurizio Pocchiari. Human Prion Diseases. Elsevier, 2018.

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34

Human Prion Diseases. Elsevier, 2018. http://dx.doi.org/10.1016/c2016-0-01756-4.

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35

Manson, Jean, and Maurizio Pocchiari. Human Prion Diseases. Elsevier, 2018.

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36

(Collaborator), Detlev Riesner, Hans Kretzschmar (Collaborator), and Beat Hornlimann (Editor), eds. Prions in Humans and Animals. Walter de Gruyter, 2006.

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37

(Editor), Holger F. Rabenau, Jindrich Cinatl (Editor), and Hans Wilhelm Doerr (Editor), eds. Prions: A Challenge for Science, Medicine and Public Health System (Contributions to Microbiology, Vol. 7). S. Karger Publishers (USA), 2001.

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38

Béringue, Vincent. Prion Biology. Taylor & Francis Group, 2021.

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39

Telling, Glenn. Prions and Prion Diseases: Current Perspectives (Horizonbioscience). Taylor & Francis, 2004.

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40

Kitamoto, Tetsuyuki. Prions: Food and Drug Safety. Springer, 2005.

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41

Kitamoto, Tetsuyuki. Prions. Springer, 2008.

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42

Prusiner, Stanley B. Prion Biology and Diseases. 2nd ed. Cold Spring Harbor Laboratory Press, 2003.

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43

Berger, Stephen, and Inc Gideon Informatics. Prion Diseases: Global Status. Gideon Informatics, Incorporated, 2022.

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44

Bennett, Clinton, and Jason G. Hartell. Guide to Prion Diseases. Hodder Education Group, 1998.

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45

Gideon science GIDEON science team. Prion Diseases: Global Status. Gideon Informatics, Incorporated, 2023.

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46

Prion Biology. Cold Spring Harbor Laboratory Press, 2017.

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47

Prusiner, Stanley B. Prion Biology. Cold Spring Harbor Laboratory Press, 2017.

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48

Sheen, Barbara. Diseases and Disorders - Mad Cow Disease (Diseases and Disorders). Lucent Books, 2004.

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49

Hope, James, and Mark P. Dagleish. Prion-protein-related diseases of animals and man. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198570028.003.0041.

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Scrapie, bovine spongiform encephalopathy (BSE), Creutzfeldt–Jakob disease (CJD), and related diseases of mink (transmissible mink encephalopathy), mule deer and elk (chronic wasting disease) are the founder members of a group of diseases called the transmissible degenerative (or spongiform) encephalopathies (TSE). These diseases can be transmitted by prions from affected to healthy animals by inoculation or by feeding diseased tissues. Prions are cellular proteins that can transfer metabolic and pathological phenotypes vertically from parent to progeny or horizontally between cells and animals. TSEs are characterised by the accumulation of the prion form of the mammalian prion protein (PrPC) in the central nervous system or peripheral tissues of animals and humans. Mutations of the human PrP gene are linked to rare, familial forms of disease and prion-protein gene polymorphisms in humans and other species are linked to survival time and disease characteristics in affected individuals. Iatrogenic transmission of CJD in man has occurred, and a variant form of CJD (vCJD) is due to cross-species transmission of BSE from cattle to humans. Atypical forms of scrapie and BSE have been identified during large-scale monitoring for TSEs worldwide. This chapter outlines our current understanding of scrapie, BSE, CJD and other TSEs and highlights recent progress in defining the role in disease of the prion protein, PrP.

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50

Prions: Current progress in advanced research. Norfolk, UK: Caister Academic Press, 2013.

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