Literature DB >> 1364008

Hidden amyloidoses.

H Diringer1.   

Abstract

The pathogenesis as well as the genetic disposition to develop clinical symptoms in transmissible spongiform encephalopathies (e.g. Creutzfeldt-Jakob disease, scrapie, bovine spongiform encephalopathy) relate these diseases to classical noninfectious amyloidoses (familial amyloidotic polyneuropathy as an example) and to Alzheimer's disease. This is not obvious to the nonexpert at first glance. This communication tries to elucidate this association, to reveal which immunochemical techniques have contributed their share.

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Year:  1992        PMID: 1364008

Source DB:  PubMed          Journal:  Exp Clin Immunogenet        ISSN: 0254-9670


  4 in total

Review 1.  Prions, beta-sheets and transmissible dementias: is there still something missing?

Authors:  P P Liberski
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

2.  Characterisation of antisera raised against species-specific peptide sequences from scrapie-associated fibril protein and their application for post-mortem immunodiagnosis of spongiform encephalopathies.

Authors:  U Oberdieck; Y G Xi; M Pocchiari; H Diringer
Journal:  Arch Virol       Date:  1994       Impact factor: 2.574

3.  Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease.

Authors:  M Salvatore; M Genuardi; R Petraroli; C Masullo; M D'Alessandro; M Pocchiari
Journal:  Hum Genet       Date:  1994-10       Impact factor: 4.132

Review 4.  Prions and related neurological diseases.

Authors:  M Pocchiari
Journal:  Mol Aspects Med       Date:  1994
  4 in total

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