Please use this identifier to cite or link to this item:
http://repo.knmu.edu.ua/handle/123456789/6182
Full metadata record
DC Field | Value | Language |
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dc.contributor.advisor | Zolotaikina, Viktoriia | - |
dc.contributor.author | Ithar Mohamed Taha | - |
dc.contributor.author | Khulood Ebrahim | - |
dc.contributor.author | Золотайкіна, Вікторія Ігорівна | - |
dc.date.accessioned | 2014-06-02T06:59:54Z | - |
dc.date.available | 2014-06-02T06:59:54Z | - |
dc.date.issued | 2014-05 | - |
dc.identifier.citation | Ithar Mohamed Taha. Clinical features of Brugada syndrome / Ithar Mohamed Taha, Khulood Ebrahim, V. Zolotaikina // 7th International Scientific Interdisci-plinary Conference for medical students and young scientists, Kharkiv, May 15–16, 2014 : abstract book / Kharkiv National Medical University. – Kharkiv, 2014. – Р. 79. | uk_UA |
dc.identifier.uri | https://repo.knmu.edu.ua/handle/123456789/6182 | - |
dc.description.abstract | We conclude that electrocardiographic characteristics of long QT interval (QT) syndrome type 3 (LQT3) and Brugada syndrome (BS) show age-dependent penetrance. A QT prolongation and conduction disease were present from birth onwards, whereas ST-segment elevation only developed >5 years. Good tools for clinical diagnosis of LQT3 in this family are QTc at the lowest HR and ΔQT after a pause in a Holter, even at very young age. | uk_UA |
dc.language.iso | en | uk_UA |
dc.subject | вrugada syndrome | uk_UA |
dc.subject | SNC5A mutation | uk_UA |
dc.subject | long QT interval (QT) syndrome type 3 | uk_UA |
dc.title | Clinical features of Brugada syndrome | uk_UA |
dc.type | Thesis | uk_UA |
Appears in Collections: | Наукові роботи молодих вчених. Кафедра внутрішньої медицини № 2 і клінічної імунології та алергології ім. ак. Л.Т. Малої |
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File | Description | Size | Format | |
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Ithar Mohamed Taha - abstract-oral-50.doc | 29,5 kB | Microsoft Word | View/Open |
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