| dc.contributor.author | Andic, Cagatay | |
| dc.contributor.author | Gunesli, Aylin | |
| dc.contributor.author | Alkan, Ozlem | |
| dc.contributor.author | Erol, Ilknur | |
| dc.contributor.author | Suner, Halil Ibrahim | |
| dc.date.accessioned | 2019-05-06T13:19:36Z | |
| dc.date.available | 2019-05-06T13:19:36Z | |
| dc.date.issued | 2018 | |
| dc.identifier.issn | 1817-1745 | |
| dc.identifier.uri | http://www.pediatricneurosciences.com/article.asp?issn=1817-1745;year=2018;volume=13;issue=2;spage=245;epage=248;aulast=Gunesli | |
| dc.identifier.uri | http://hdl.handle.net/11727/3199 | |
| dc.description.abstract | Seckel syndrome and Moyamoya diseases are different entities that rarely associated with each other. Several cases presenting with both these diseases were reported. Intracerebral artery aneurysms and collateral vessels can be seen with Moyamoya. They are commonly treated with medical treatment. We present a 12-years old patient with both Seckel syndrome and Moyamoya disease presented with middle cerebral artery aneurysm which was treated with endovascular modalities. | en_US |
| dc.language.iso | eng | en_US |
| dc.relation.isversionof | 10.4103/jpn.JPN_96_17 | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Endovascular treatment | en_US |
| dc.subject | Intracranial aneurysm | en_US |
| dc.subject | Moyamoya disease | en_US |
| dc.subject | Seckel syndrome | en_US |
| dc.title | Endovascular Treatment of a Patient with Moyamoya Disease and Seckel Syndrome: A Case Report | en_US |
| dc.type | article | en_US |
| dc.relation.journal | JOURNAL OF PEDIATRIC NEUROSCIENCES | en_US |
| dc.identifier.volume | 13 | en_US |
| dc.identifier.issue | 2 | en_US |
| dc.identifier.startpage | 245 | en_US |
| dc.identifier.endpage | 248 | en_US |
| dc.identifier.wos | 000438560700025 | en_US |
| dc.identifier.scopus | 2-s2.0-85049856424 | en_US |
| dc.contributor.pubmedID | 30090148 | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | en_US |
