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Choroba Creutzfeldta-Jakoba i inne choroby wywołane przez priony - pasażowalne encefalopatie gąbczaste człowieka
8389309068
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Description
W książce tej autor zajmuje się omówieniem grupy chorób neurozwyrodnieniowych, charakteryzujących się odkładaniem w ośrodkowym układzie nerwowym (i niektórych innych tkankach) nieprawidłowej izoformy białka prionu, PrPSc. U człowieka do tej grupy zalicza się:: kuru, chorobę Creutzfeldta-Jakoba (CJD), chorobę Gerstmanna-Sträusslera-Scheinkera (GSS), śmiertelną rodzinną bezsenność (FFI) oraz sporadyczną odmianę tej choroby - śmiertelną sporadyczną bezsenność (FSI). Najwięcej uwagi autor poświęcił przedstawieniu choroby Creutzfeldta-Jakoba. Wspomniane zostały oryginalne przypadki opisane przez Jakoba i Creutzfeldta, omówiono objawy kliniczne tej choroby, badania laboratoryjne i neuropatologiczne oraz odmiany CJD. Dodatkową zaletą tej publikacji jest bardzo obszerna bibliografia.
Product Details
2972
9788389309068
83-89309-06-8
Data sheet
- Published in
- Lublin
- Publication date
- 2003
- Issue number
- 1
- Cover
- paperback
- Pages count
- 124
- Dimensions (mm)
- 160 x 235
- Weight (g)
- 240
- 1. Definicje i klasyfikacje
- 2. Wstęp historyczny
- 3. Teoria prionu
- 4. Choroba Creutzfeldta-Jakoba
- 5. Choroba Gerstmanna-Sträusslera-Scheinkera
- 5. Odmiana wzgórzowa CJD i śmiertelna rodzinna bezsenność
- 6. Kuru
- 7. Dekontaminacja
- Piśmiennictwo
- Indeks
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