Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Furkan ÖZDEN"'
Autor:
Enes YAVUZ, Merve GİRİCİ, Furkan ÖZDEN, Şeyma BARAN, Hüsna DURAN, Efekan YILMAZ, Diyap SERİN, Gülsüm ÖZKAN
Publikováno v:
Namık Kemal Tıp Dergisi, Vol 5, Iss 3, Pp 118-121 (2017)
Aim:Hypertension (HT) is a common disease worldwide and in Turkey. The prevalence of HT in Turkey is 31.8%. HT is also a costly disease that affects important vital organs, leading to significant morbidity and mortality. The most important feature of
Externí odkaz:
https://doaj.org/article/27fc764b6cb549feb246045391ea65ad
Publikováno v:
Medical Science and Discovery. 10:348-352
Objective: The objective of this study was to comprehensively evaluate occupational accidents in a hospital setting using the L-Type matrix and Fine-Kinney risk assessment methods. The aim was to assess the frequency, severity, and associated risks o
Copy number variants (CNV) are shown to contribute to the etiology of several genetic disorders. Accurate detection of CNVs on whole exome sequencing (WES) data has been a long sought after goal for use in clinic. This was not possible despite recent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a9256341ba4785bc16617c3bf9c153c
https://doi.org/10.1101/2022.11.17.516880
https://doi.org/10.1101/2022.11.17.516880
Publikováno v:
Journal of Surgery and Medicine, Vol 3, Iss 12, Pp 891-893 (2019)
Volume: 3, Issue: 12 891-893
Journal of Surgery and Medicine
Volume: 3, Issue: 12 891-893
Journal of Surgery and Medicine
Multiple myeloma (MM), neoplastic proliferation of monoclonal plasma cells in bone marrow, constitutes 1% of cancers. We discuss a rare case of newly diagnosed MM presenting to the emergency department with sudden strength loss in both legs and inabi
Publikováno v:
Genome research
Accurate and efficient detection of copy number variants (CNVs) is of critical importance due to their significant association with complex genetic diseases. Although algorithms working on whole genome sequencing (WGS) data provide stable results wit
Autor:
Berk Mandiracioglu, Furkan Ozden, Gun Kaynar, Mehmet Alper Yilmaz, Can Alkan, A. Ercument Cicek
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-13 (2024)
Abstract Copy number variants (CNV) are shown to contribute to the etiology of several genetic disorders. Accurate detection of CNVs on whole exome sequencing (WES) data has been a long sought-after goal for use in clinics. This was not possible desp
Externí odkaz:
https://doaj.org/article/2c0f75509a0a44c99b983e360d0ad289
Publikováno v:
Volume: 10, Issue: 4 101-104
Journal of Emergency Medicine Case Reports
Journal of Emergency Medicine Case Reports
Introduction: Large vessel and cardiac injuries may also be seen in high-energy blunt traumas such as traffic accidents. This report describes a multitrauma patient with vena cava isthmus inferior injury brought to the emergency department following
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c198e0f6d830da34959078916588e35b
https://dergipark.org.tr/tr/pub/jemcr/issue/51803/516924
https://dergipark.org.tr/tr/pub/jemcr/issue/51803/516924