Literature DB >> 11051298

The prion diseases.

J A Mastrianni1, R P Roos.   

Abstract

The prion diseases constitute an unusual group of neurodegenerative disorders. Although they are similar in many ways to other more common diseases, such as Alzheimer disease and amyotrophic lateral sclerosis, they are set apart on the basis of their transmissible nature. In addition to the unique feature of transmissibility, the prion diseases demonstrate that the expression of diverse disease phenotypes is possible from a common etiologic factor. This review provides the reader with a basic understanding of the nature of prions and highlights the clinical and pathologic features of these fascinating diseases.

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Year:  2000        PMID: 11051298     DOI: 10.1055/s-2000-9396

Source DB:  PubMed          Journal:  Semin Neurol        ISSN: 0271-8235            Impact factor:   3.420


  4 in total

Review 1.  Presenile dementia syndromes: an update on taxonomy and diagnosis.

Authors:  M D Greicius; M D Geschwind; B L Miller
Journal:  J Neurol Neurosurg Psychiatry       Date:  2002-06       Impact factor: 10.154

2.  Live cell fluorescence resonance energy transfer predicts an altered molecular association of heterologous PrPSc with PrPC.

Authors:  Suparna Mallik; Wenbin Yang; Eric M Norstrom; James A Mastrianni
Journal:  J Biol Chem       Date:  2010-01-19       Impact factor: 5.157

3.  Syndromes of Rapidly Progressive Cognitive Decline-Our Experience.

Authors:  Sadanandavalli Retnaswami Chandra; Lakshminarayanapuram Gopal Viswanathan; Anupama Ramakanth Pai; Rahul Wahatule; Suvarna Alladi
Journal:  J Neurosci Rural Pract       Date:  2017-08

Review 4.  Infectious agents and age-related neurodegenerative disorders.

Authors:  Mark P Mattson
Journal:  Ageing Res Rev       Date:  2004-01       Impact factor: 10.895

  4 in total

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