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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/5756
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dc.contributor.authorKimber, T.-
dc.contributor.authorBlumbergs, P.-
dc.contributor.authorRice, J.-
dc.contributor.authorHallpike, J.-
dc.contributor.authorEdis, R.-
dc.contributor.authorThompson, P.-
dc.contributor.authorSuthers, G.-
dc.date.issued1998-
dc.identifier.citationJournal of the Neurological Sciences, 1998; 160(1):33-40-
dc.identifier.issn0022-510X-
dc.identifier.issn1878-5883-
dc.identifier.urihttp://hdl.handle.net/2440/5756-
dc.description.abstractFemale monozygotic twins developed upper and lower limb neurogenic weakness in their thirties, followed by cerebellar ataxia, dysarthria and death after an illness duration of about 20 years. Autopsy revealed pathological features typical of neuronal intranuclear inclusion disease (NIID) and positive ubiquitin immunostaining of the inclusions. Two adult sons of one of the twins have now developed an identical illness. This family provides strong evidence of an hereditary form of NIID.-
dc.description.statementofresponsibilityKimber, T.E; Blumbergs, P.C; Rice, J.P; Hallpike, J.F; Edis, R; Thompson, P.D; Suthers, G-
dc.language.isoen-
dc.publisherElsevier BV-
dc.source.urihttp://dx.doi.org/10.1016/s0022-510x(98)00169-5-
dc.subjectInclusion Bodies-
dc.subjectHumans-
dc.subjectNeurodegenerative Diseases-
dc.subjectDiseases in Twins-
dc.subjectNerve Tissue Proteins-
dc.subjectUbiquitins-
dc.subjectFatal Outcome-
dc.subjectPedigree-
dc.subjectTwins, Monozygotic-
dc.subjectGenes, Dominant-
dc.subjectAdult-
dc.subjectFemale-
dc.titleFamilial neuronal intranuclear inclusion disease with ubiquitin positive inclusions-
dc.typeJournal article-
dc.identifier.doi10.1016/S0022-510X(98)00169-5-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest
Pathology publications

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