Literature DB >> 12432830

Inherited dementias.

Peter Hedera1, R Scott Turner.   

Abstract

Dementia, defined as progressive cognitive decline, is a feature of a wide variety of genetic disorders. For example, a search of "dementia" in the Online Mendelian Inheritance in Man (www.ncbi.nlm.nih.gov/Omim) reveals 162 entries. Therefore this article cannot be encyclopedic and will be necessarily restricted to more prevalent or illustrative etiologies of familial dementia in adults. These disorders also have in common an initial and primarily dementing clinical presentation. Thus, this article is limited to: familial Alzheimer's disease (AD) and related amyloid angiopathies, frontotemporal dementias (FTD) and related tauopathies, familial prion diseases, British and Danish familial dementias, and cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

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Year:  2002        PMID: 12432830     DOI: 10.1016/s0733-8619(01)00020-2

Source DB:  PubMed          Journal:  Neurol Clin        ISSN: 0733-8619            Impact factor:   3.806


  2 in total

1.  APP and APLP1 are degraded through autophagy in response to proteasome inhibition in neuronal cells.

Authors:  Fangfang Zhou; Theo van Laar; Huizhe Huang; Long Zhang
Journal:  Protein Cell       Date:  2011-05-28       Impact factor: 14.870

2.  Is abnormal axonal transport a cause, a contributing factor or a consequence of the neuronal pathology in Alzheimer's disease?

Authors:  Virgil Muresan; Zoia Muresan
Journal:  Future Neurol       Date:  2009-11-01
  2 in total

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