Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12262
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dc.contributor.authorCorben, Louise Aen
dc.contributor.authorKashuk, Saman Ren
dc.contributor.authorAkhlaghi, Hameden
dc.contributor.authorJamadar, Sharnaen
dc.contributor.authorDelatycki, Martin Ben
dc.contributor.authorFielding, Joanneen
dc.contributor.authorJohnson, Bethen
dc.contributor.authorGeorgiou-Karistianis, Nellieen
dc.contributor.authorEgan, Gary Fen
dc.date.accessioned2015-05-16T01:55:21Z
dc.date.available2015-05-16T01:55:21Z
dc.date.issued2014-06-02en
dc.identifier.citationJournal of the Neurological Sciences 2014; 343(1-2): 138-43en
dc.identifier.govdoc24930398en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/12262en
dc.description.abstractThe dentate nucleus (DN) is the major relay station for neural connection between the cerebellum and cerebrum via the thalamus, and is a significant component of the neuropathological profile of Friedreich ataxia (FRDA). We have previously shown that the size of the superior cerebellar peduncle (SCP), which links the DN to cortical and subcortical structures via the thalamus, is significantly reduced in individuals with FRDA compared to control participants. This study used magnetization transfer imaging (MTI) to examine and contrast the integrity of white matter (WM) in the SCP and the corpus callosum (CC) (control region) in ten individuals with FRDA and ten controls. Individuals with FRDA demonstrated a significant reduction in the magnetization transfer ratio (MTR) in the SCP compared to control participants. However, there was no significant difference between groups in MTR in the CC. When comparing regions within groups, there was a significant reduction in MTR in the SCP compared to CC in participants with FRDA only. We suggest that the reduction in MTR in the SCP may be indicative of lack of myelin secondary to axonal loss and oligodendroglial dysfunction in WM tracts in individuals with FRDA.en
dc.language.isoenen
dc.subject.otherAxonopathyen
dc.subject.otherFrataxinen
dc.subject.otherFriedreich ataxiaen
dc.subject.otherMagnetization transfer ratioen
dc.subject.otherMyelinen
dc.subject.otherOligodendrocytesen
dc.subject.otherAdulten
dc.subject.otherAnisotropyen
dc.subject.otherCerebellum.pathologyen
dc.subject.otherCorpus Callosum.pathologyen
dc.subject.otherDiffusion Tensor Imagingen
dc.subject.otherFemaleen
dc.subject.otherFriedreich Ataxia.pathologyen
dc.subject.otherHumansen
dc.subject.otherImage Processing, Computer-Assisteden
dc.subject.otherMaleen
dc.subject.otherMiddle Ageden
dc.subject.otherMyelin Sheath.pathologyen
dc.subject.otherNerve Fibers, Myelinated.pathologyen
dc.subject.otherPons.pathologyen
dc.subject.otherSeverity of Illness Indexen
dc.subject.otherStatistics as Topicen
dc.subject.otherYoung Adulten
dc.titleMyelin paucity of the superior cerebellar peduncle in individuals with Friedreich ataxia: an MRI magnetization transfer imaging study.en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of the neurological sciencesen
dc.identifier.affiliationDepartment of Clinical Genetics, Austin Health, Heidelberg, Victoria 3084, Australiaen
dc.identifier.affiliationMonash Biomedical Imaging, Monash University, Clayton, Victoria 3800, Australiaen
dc.identifier.affiliationSchool of Psychological Sciences, Monash University, Clayton, Victoria 3800, Australiaen
dc.identifier.affiliationMonash Medical Centre, Monash Health, Clayton, Victoria 3168, Australiaen
dc.identifier.affiliationBruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Parkville 3052, Victoria, Australiaen
dc.identifier.affiliationCollege of Engineering and Science, Victoria University, Melbourne 8001, Victoria, Australiaen
dc.identifier.doi10.1016/j.jns.2014.05.057en
dc.description.pages138-43en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/24930398en
dc.type.austinJournal Articleen
local.name.researcherDelatycki, Martin B
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptClinical Genetics-
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