Zobrazeno 1 - 10 of 63 pro vyhledávání: '"Ömer BEKTAŞ"'
1
Akademický článek
Investigating the Impact on Long-Term Outcomes and the Necessity of Hereditary Thrombophilia Screening in Presumed or Perinatal Arterial Ischemic Stroke
Autor: Ömer Bektaş MD, Özben Akıncı Göktaş MD, Begüm Atasay MD, Serap Teber MD
Publikováno v: Clinical and Applied Thrombosis/Hemostasis, Vol 30 (2024)
This study aimed to investigate the influence of prothrombotic risk factors on long-term outcomes of patients with perinatal arterial ischemic stroke. The study was conducted through an analysis of monitoring results that were regularly maintained fo
Externí odkaz: https://doaj.org/article/128eacfe47c2412bb696724ea4a0e5dc
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3
Akademický článek
A Case of Botulism Fast Adjusting with Antitoxin Administration in the Early Period and the Use of Electromyography in Diagnosis
Autor: Edin Botan, Serhan Özcan, Merve Havan, Emrah Gün, Merve Feyza Yüksel, Serdar Balsak, Özge Güzelmansur, Ömer Bektaş, Tanıl Kendirli
Publikováno v: Journal of Pediatric Emergency and Intensive Care Medicine, Vol 8, Iss 2, Pp 114-116 (2021)
Botulism is a rare but potentially life-threatening neuroparalytic syndrome caused by the action of a neurotoxin caused by the bacterium Clostridium botulinum. Early diagnosis and early treatment is important. In cases where botulism occurs sporadica
Externí odkaz: https://doaj.org/article/d2699e741a60486887ab0bb666a70ade
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4
Akademický článek
A sydenham chorea attack associated with COVID-19 infection
Autor: Merve Feyza Yüksel, Miraç Yıldırım, Ömer Bektaş, Süleymen Şahin, Serap Teber
Publikováno v: Brain, Behavior, & Immunity - Health, Vol 13, Iss , Pp 100222- (2021)
The coronavirus disease 2019 (COVID-19) caused by SARS-CoV-2 appeared in Wuhan, China in December 2019 and quickly spread around the world and is considered a global pandemic. This disease, which is pre-infected with respiratory and cardiovascular sy
Externí odkaz: https://doaj.org/article/9d9511c1a79847919e17dd8e40af5d9a
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6
A Case of Multidrug-Resistant Lance-Adams Syndrome Successfully Treated With Phenobarbital
Autor: Nurşah Yeniay Süt, Miraç Yıldırım, Ömer Bektaş, Tanıl Kendirli, Serap Teber
Publikováno v: Clinical Neuropharmacology. 46:34-37
Lance-Adams syndrome is a rare but devastating disorder characterized by rest, action, and stimulus-sensitive myoclonus after cardiorespiratory arrest. We aimed to present a case of multidrug-resistant Lance-Adams syndrome that was successfully treat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1254d738837c7f1db1932b58632fd7e
https://doi.org/10.1097/wnf.0000000000000532
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7
A Case of Combined Oxidative Phosphorylation Deficiency 35 Associated with a Novel Missense Variant of the TRIT1 Gene
Autor: Serap Teber, Ömer Bektaş, Miraç Yıldırım, Nurşah Yeniay Süt, Yavuz Sayar, Ümmühan Öncül, Ebru Tuncez
Publikováno v: Molecular Syndromology. 13:139-145
Combined oxidative phosphorylation deficiency 35 (COXPD35) is a rare autosomal recessive disorder associated with homozygous or compound heterozygous mutations in the tRNA isopentenyltransferase (TRIT1) gene in chromosome 1p34.2. To date, only 10 typ
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a004259caa3f182b88abe346c3025310
https://doi.org/10.1159/000518373
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8
Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes
Autor: Ünsal Yılmaz, Kıvılcım Gücüyener, Merve Yavuz, İbrahim Öncel, Mehmet Canpolat, Sema Saltık, Olcay Ünver, Ayşegül Neşe Çıtak Kurt, Ayşe Tosun, Sanem Yılmaz, Bilge Özgör, İlknur Erol, Ülkühan Öztoprak, Duygu Aykol Elitez, Meltem Çobanoğulları Direk, Muhittin Bodur, Serap Teber, Banu Anlar, Sema Saltik, Duygu Aykol, Edibe Pembegül Yıldız, Coşkun Yarar, Bülent Kara, Şenay Haspolat, Faruk İncecik, Gültekin Kutluk, Cengiz Dilber, Nihal Olgac Dundar, Hüseyin Tan, Ercan Demir, Büşra Daşlı Dursun, Tuğçe Damla Dilek, Dilşad Türkdoğan, Dilek Yalnızoğlu, Salih Akbaş, Ayten Güleç, Deniz Yılmaz, Müge Ayanoğlu, Seda Kanmaz, Serdal Güngör, Gülten Öztürk, Şeyda Beşen, Göknur Haliloğlu, Nazlı Balcan Karaca, Selcan Öztürk, Deniz Yüksel, Esra Gürkaş, Seçil Oktay, Hepsen Mine Serin, Meral Karadağ, İsmail Hakkı Akbeyaz, Uluç Yiş, Burçin Gönüllü Polat, Mehmet Sait Okan, Ömer Bektaş, Leman Tekin Orgun, Ceren Günbey, Hüseyin Per, Pembe Gültutan, Semra Büyükkorkmaz Öztürk, Erhan Aksoy, Gülcan Akyüz, Hasan Tekgül, Fulya Kürekçi, A. Semra Hız Kurul, Kürşat Bora Çarman, Defne Alikılıç, Özgür Duman, Mustafa Kömür, Miraç Yıldırım, Nurettin Alıcı, Hakan Gümüş, Muzaffer Polat, Bahadır Konuşkan, Olcay Güngör, Gülen Gül Mert, Selvinaz Edizer, Filiz Mıhçı, Sedef Terzioğlu Öztürk, Rabia Tütüncü Toker, Mutluay Arslan, Sevim Şahin, Pinar Gencpinar, Elif Yıldırım, Ersin Yüksel, Arzu Ekici, Adnan Deniz, Özlem Yayici Köken, Çetin Okuyaz, Nurşah Yeniay Süt, Ergin Atasoy, İsmail Solmaz, Mehmet Fatih Yetkin, Neslihan Bilgin, Aslı Kübra Atasever, Hande Gazeteci Tekin, İpek Dokurel, Aysima Özçelik, Ayşe Aksoy, Ayşe Nur Türköz, Dilek Cavusoglu, Mehbare Özkan, Emine Tekin, Türkan Uygur Şahin, Aycan Ünalp, Habibe Koç, Esra Sarıgeçili, Serdar Sarıtaş, Senem Ayça, Hülya Kayılıoğlu, Mine Çiğdem Şenoğlu, Tülay Kamaşak, Nargis Asadova, Filiz Keskin, Pakize Karaoğlu, Rojan İpek, Hamit Acer
Background: The discovery of anti-myelin oligodendrocyte glycoprotein (MOG)-IgG and anti-aquaporin 4 (AQP4)-IgG and the observation on certain patients previously diagnosed with multiple sclerosis (MS) actually have an antibody-mediated disease manda
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7189bb594b8e7e139069b7085c4d9385
https://avesis.deu.edu.tr/publication/details/e770a716-7c76-47b6-ae1a-6a20fb66ce13/oai
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