Please use this identifier to cite or link to this item:
https://open.uns.ac.rs/handle/123456789/9228
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Pavlović, Aleksandra | en |
dc.contributor.author | Dobricic V. | en |
dc.contributor.author | Semnic R. | en |
dc.contributor.author | Lackovic V. | en |
dc.contributor.author | Novakovic I. | en |
dc.contributor.author | Bajcetic M. | en |
dc.contributor.author | Sternic N. | en |
dc.date.accessioned | 2019-09-30T09:14:23Z | - |
dc.date.available | 2019-09-30T09:14:23Z | - |
dc.date.issued | 2013-01-01 | en |
dc.identifier.issn | 03009009 | en |
dc.identifier.uri | https://open.uns.ac.rs/handle/123456789/9228 | - |
dc.description.abstract | Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common heritable cause of stroke and vascular dementia in adults. We present a family from Serbia presenting with stroke and depression in the lack of vascular risk factors, with brain MRI indicating CADASIL. A novel NOTCH3 Gly89Cys mutation was located in exon 3. This report illustrates that in the setting of a positive family history with typical clinical and MRI features, even with an atypical form of pedigree, a high suspicion of CADASIL should lead to genetic testing. © 2013 Belgian Neurological Society. | en |
dc.relation.ispartof | Acta Neurologica Belgica | en |
dc.title | A novel Notch3 Gly89Cys mutation in a Serbian CADASIL family | en |
dc.type | Journal/Magazine Article | en |
dc.identifier.doi | 10.1007/s13760-012-0174-2 | en |
dc.identifier.pmid | 113 | en |
dc.identifier.scopus | 2-s2.0-84883393935 | en |
dc.identifier.url | https://api.elsevier.com/content/abstract/scopus_id/84883393935 | en |
dc.relation.lastpage | 302 | en |
dc.relation.firstpage | 299 | en |
dc.relation.issue | 3 | en |
dc.relation.volume | 113 | en |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
Appears in Collections: | Naučne i umetničke publikacije |
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