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http://hdl.handle.net/11452/32646
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Cangül, Hakan | - |
dc.date.accessioned | 2023-05-12T11:18:41Z | - |
dc.date.available | 2023-05-12T11:18:41Z | - |
dc.date.issued | 2013-06 | - |
dc.identifier.citation | Temel, Ş. G. vd. (2013). “Turkish perspective of Jervell and Lange-Nielsen syndrome”. Annals of Indian Academy of Neurology, 16(1), 129-130. | en_US |
dc.identifier.issn | 0972-2327 | - |
dc.identifier.issn | 1998-3549 | - |
dc.identifier.uri | https://doi.org/10.4103/0972-2327.107703 | - |
dc.identifier.uri | https://journals.lww.com/annalsofian/Fulltext/2013/16010/Turkish_perspective_of_Jervell_and_Lange_Nielsen.29.aspx | - |
dc.identifier.uri | http://hdl.handle.net/11452/32646 | - |
dc.language.iso | en | en_US |
dc.publisher | Wolters Kluwer Medknow Publications | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.rights | Atıf Gayri Ticari Türetilemez 4.0 Uluslararası | tr_TR |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | Neurosciences & neurology | en_US |
dc.subject | Deafness | en_US |
dc.subject | Children | en_US |
dc.title | Turkish perspective of Jervell and Lange-Nielsen syndrome | en_US |
dc.type | Letter | en_US |
dc.identifier.wos | 000316907100029 | tr_TR |
dc.identifier.scopus | 2-s2.0-84875695272 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı. | tr_TR |
dc.contributor.orcid | 0000-0002-9802-0880 | tr_TR |
dc.contributor.orcid | 0000-0001-7707-2174 | tr_TR |
dc.contributor.orcid | 0000-0003-3516-0082 | tr_TR |
dc.identifier.startpage | 129 | tr_TR |
dc.identifier.endpage | 130 | tr_TR |
dc.identifier.volume | 16 | tr_TR |
dc.identifier.issue | 1 | tr_TR |
dc.relation.journal | Annals of Indian Academy of Neurology | en_US |
dc.contributor.buuauthor | Temel, Şehime Gülsün | - |
dc.contributor.buuauthor | Bostan, Özlem Mehtap | - |
dc.contributor.buuauthor | Çil, Ergün | - |
dc.contributor.researcherid | AAG-8385-2021 | tr_TR |
dc.contributor.researcherid | AAG-9324-2021 | tr_TR |
dc.contributor.researcherid | AAG-8558-2021 | tr_TR |
dc.relation.collaboration | Yurt dışı | tr_TR |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.identifier.pubmed | 23661983 | tr_TR |
dc.subject.wos | Clinical neurology | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q4 | en_US |
dc.contributor.scopusid | 6507885442 | tr_TR |
dc.contributor.scopusid | 8676936500 | tr_TR |
dc.contributor.scopusid | 35587943300 | tr_TR |
dc.subject.scopus | Potassium Channels; Jervell-Lange Nielsen Syndrome; Torsade Des Pointes | en_US |
dc.subject.emtree | Echocardiography | en_US |
dc.subject.emtree | Exercise test | en_US |
dc.subject.emtree | Faintness | en_US |
dc.subject.emtree | Family history | en_US |
dc.subject.emtree | Hearing impairment | en_US |
dc.subject.emtree | Heart depolarization | en_US |
dc.subject.emtree | Holter monitoring | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Letter | en_US |
dc.subject.emtree | Long QT syndrome | en_US |
dc.subject.emtree | Turkey (republic) | en_US |
Appears in Collections: | Scopus Web of Science |
Files in This Item:
File | Description | Size | Format | |
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Şehime_vd_2013.pdf | 382.82 kB | Adobe PDF | View/Open |
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