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Difference between revisions of "Neurodegenerative diseases"
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→Prion diseases
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*Creutzfeldt-Jakob disease (CJD). | *Creutzfeldt-Jakob disease (CJD). | ||
*Sporadic fatal insomnia (sFI).<ref name=pmid16609731>{{cite journal |author=Watts JC, Balachandran A, Westaway D |title=The expanding universe of prion diseases |journal=PLoS Pathog. |volume=2 |issue=3 |pages=e26 |year=2006 |month=March |pmid=16609731 |pmc=1434791 |doi=10.1371/journal.ppat.0020026 |url=}}</ref> | *Sporadic fatal insomnia (sFI).<ref name=pmid16609731>{{cite journal |author=Watts JC, Balachandran A, Westaway D |title=The expanding universe of prion diseases |journal=PLoS Pathog. |volume=2 |issue=3 |pages=e26 |year=2006 |month=March |pmid=16609731 |pmc=1434791 |doi=10.1371/journal.ppat.0020026 |url=}}</ref> | ||
*Fatal familial insomnia (FFI).<ref name=Ref_PCPBoD8_672>{{Ref PCPBoD8|672}}</ref> | *Fatal familial insomnia (FFI).<ref name=Ref_PCPBoD8_672>{{Ref PCPBoD8|672}}</ref><ref name=omim600072>{{OMIM|600072}}</ref> | ||
*Gestmann-Straussler-Scheinker syndrome (GSS) - due to PRNP gene mutations.<ref name=Ref_PCPBoD8_671>{{Ref PCPBoD8|671}}</ref> | *Gestmann-Straussler-Scheinker syndrome (GSS) - due to PRNP gene mutations.<ref name=Ref_PCPBoD8_671>{{Ref PCPBoD8|671}}</ref> | ||