2019
DOI: 10.1007/s12017-019-08537-7
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Intracranial Aneurysms: Pathology, Genetics, and Molecular Mechanisms

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Cited by 76 publications
(60 citation statements)
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References 180 publications
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“…There is no significant overlap in putative susceptibility genes between various ES-based studies [35], which may reflect a pronounced heterogeneity of IA/SAH pathogenesis. We also aimed to identify genetic risk factors for UIA/aSAH by a family-based ES approach, and we propose EDIL3 as new risk gene.…”
Section: Genetic and Functional Aspects On Edil3 As An Uia/ Asah Riskmentioning
confidence: 97%
“…There is no significant overlap in putative susceptibility genes between various ES-based studies [35], which may reflect a pronounced heterogeneity of IA/SAH pathogenesis. We also aimed to identify genetic risk factors for UIA/aSAH by a family-based ES approach, and we propose EDIL3 as new risk gene.…”
Section: Genetic and Functional Aspects On Edil3 As An Uia/ Asah Riskmentioning
confidence: 97%
“…Intracranial aneurysm is local dilatation in cerebral arteries, and about 2–5% cases can develop to rupture ( Xu et al, 2019 ). Smooth muscle cells are one key cell type-forming media in intracranial arteries and have significant roles in intracranial aneurysm formation and rupture ( Starke et al, 2014 ).…”
Section: Discussionmentioning
confidence: 99%
“…Disamping itu, sekitar 7-20%, diketahui bahwa pasien yang memiliki riwayat keluarga, dan kerabat dekat berisiko lebih tinggi, terlepas dari latar belakang etnisnya. 6 Aneurisma karotis kavernosa (AKK) merupakan suatu penyebab patologi yang tidak umum karena letak aneurisma pada ruang ekstradural. Apabila ukuran aneurismanya kecil maka tidak akan berisiko terjadinya perdarahan subaraknoid, namun apabila ukurannya besar akan menimbulkan tanda dan gejala berupa efek penekanan massa.…”
Section: Pembahasanunclassified