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Prion diseases

Author: Pierluigi Gambetti
Publisher: London : Henry Stewart Talks, 2007.
Series: Henry Stewart talks., Biomedical & life sciences collection., Neurodegenerative diseases : fundamentals, research methods, latest advances.
Edition/Format:   eVideo : Clipart/images/graphics : EnglishView all editions and formats
Summary:
Audio-visual presentation : Normal function of prion protein ; Prion diseases ; Mechanism of propagation of PrP ; Propagation in acquired and familial forms ; Pathogenic hypothesis ; Human pathogenic mutation and polymorphisms ; Laboratory methods ; Epidemiology ; Sporadic prion diseases ; New variant CJD ; Treatment of prion disease.
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Details

Material Type: Clipart/images/graphics, Internet resource, Videorecording
Document Type: Internet Resource, Computer File, Visual material
All Authors / Contributors: Pierluigi Gambetti
OCLC Number: 310380816
Notes: Title from title frames.
Animated audio-visual presentation with synchronized narration.
Description: 1 streaming video file (53 min.) : digital, mono, SWF file, sound, color.
Details: Mode of access: World Wide Web.; System requirements: Operating System: PC Windows 2000+, Mac OSX+ 3.2. Browser Compatibility: IE6+, Firefox 2+, Opera 9+, Safari 2+ 3.3. Browser settings: enable JavaScript, enable popups from the Henry Stewart Talks site. 3.4. Required Browser Plugins & Viewers: Adobe (Macromedia) Flash Player 7+, Adobe Acrobat Reader 6.0+.
Contents: Normal function of prion protein --
Prion diseases --
Mechanism of propagation of PrP --
Propagation in acquired and familial forms --
Pathogenic hypothesis --
Human pathogenic mutation and polymorphisms --
Laboratory methods --
Epidemiology --
Sporadic prion diseases --
New variant CJD --
Treatment of prion disease.
Series Title: Henry Stewart talks., Biomedical & life sciences collection., Neurodegenerative diseases : fundamentals, research methods, latest advances.
Responsibility: Pierluigi Gambetti.
More information:

Abstract:

Audio-visual presentation : Normal function of prion protein ; Prion diseases ; Mechanism of propagation of PrP ; Propagation in acquired and familial forms ; Pathogenic hypothesis ; Human pathogenic mutation and polymorphisms ; Laboratory methods ; Epidemiology ; Sporadic prion diseases ; New variant CJD ; Treatment of prion disease.

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