Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/10013
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dc.contributor.authorNovakovic, K E-
dc.contributor.authorVillemagne, Victor L-
dc.contributor.authorRowe, Christopher C-
dc.contributor.authorMasters, Colin L-
dc.date.accessioned2015-05-15T23:19:32Z
dc.date.available2015-05-15T23:19:32Z
dc.date.issued2005-
dc.identifier.citationInternational Psychogeriatrics / Ipa; 17 Suppl 1(): S149-94en
dc.identifier.otherPUBMEDen
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/10013en
dc.description.abstractSeveral genetic disorders, though rare, are associated or present with dementia. Developments in the field of genetics are contributing to clarify and expand our knowledge of the complex physiopathological mechanisms leading to neurodegeneration and cognitive decline. Disorders associated with misfolded and aggregated proteins and lipid, metal or energy metabolism are examples of the multifarious disease processes converging in the clinical features of dementia, either as its predominant feature, as in cases of Alzheimer's disease (AD) or frontotemporal dementia (FTD), or as part of a cohort of accompanying or late-developing symptoms, as in Parkinson's disease (PD) or amyotrophic lateral sclerosis with dementia (ALS-D). Awareness of these disorders, allied with recent advances in genetic, biochemical and neuroimaging techniques, may lead to early diagnosis, successful treatment and better prognosis.en
dc.language.isoenen
dc.subject.otherAmyotrophic Lateral Sclerosis.complicationsen
dc.subject.otherDementia.complications.diagnosis.geneticsen
dc.subject.otherDiagnosis, Differentialen
dc.subject.otherEnergy Metabolism.physiologyen
dc.subject.otherGerstmann-Straussler-Scheinker Disease.geneticsen
dc.subject.otherHumansen
dc.subject.otherHuntington Disease.complicationsen
dc.subject.otherInsomnia, Fatal Familial.complications.geneticsen
dc.subject.otherLipoproteins.metabolismen
dc.subject.otherNerve Degeneration.complicationsen
dc.subject.otherProteins.metabolismen
dc.subject.otherSpinocerebellar Ataxias.complicationsen
dc.subject.otherSupranuclear Palsy, Progressive.complicationsen
dc.titleRare genetically defined causes of dementia.en
dc.typeJournal Articleen
dc.identifier.journaltitleInternational psychogeriatrics / IPAen
dc.identifier.affiliationDepartment of Nuclear Medicine, Centre for PET Austin Hospital, Melbourne, Victoria, Australiaen
dc.description.pagesS149-94en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/16240489en
dc.type.contentTexten
dc.type.austinJournal Articleen
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
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