Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Özlem YAYICI KÖKEN"'
Autor:
Hülya Kayılıoğlu, Özlem Yayıcı Köken
Publikováno v:
Northwestern Medical Journal, Vol 3, Iss 3 (2023)
Aim: This study aimed to define important clinical and laboratory features that may be useful in the differential diagnosis of pediatric patients who presented with temporary loss of consciousness and in whom cardiac causes had been excluded, especia
Externí odkaz:
https://doaj.org/article/8c052c78f40b41a7a1e760cbb842810b
Publikováno v:
Van Tıp Dergisi, Vol 28, Iss 3, Pp 473-478 (2021)
INTRODUCTION: Lumbar puncture (LP) is a frequently used as a diagnostical and treatment tool in the practice of pediatric neurology. Headache associated with LP directly effects the physician and the family concerning patient comfort in a negative ma
Externí odkaz:
https://doaj.org/article/ad0d1e45b86948fcb6c10010be1cc0cf
Autor:
Ülkühan Öztoprak, Erhan Aksoy, Özlem Yayıcı Köken, Ayşegül Danış, Ayşe Seçil Ekşioğlu, Nilden Tuygun, Deniz Yüksel
Publikováno v:
Journal of Pediatric Research, Vol 8, Iss 1, Pp 20-28 (2021)
Aim:The aim of this study is to analyze children with acute carbon monoxide (CO) poisoning and to present two patients with rare neuroradiological findings.Materials and Methods:We identified and reviewed the medical records of pediatric patients dia
Externí odkaz:
https://doaj.org/article/abf6ce0d4e304ac491caafcded51cfd7
Publikováno v:
JCRPE, Vol 12, Iss 1, Pp 55-62 (2020)
Objective:To determine the prevalence of obesity and metabolic syndrome (MetS) in children and adolescents with type 1 diabetes (T1D) and to compare the widely accepted and used diagnostic criteria for MetS established by the International Diabetes F
Externí odkaz:
https://doaj.org/article/9a730d2dbed84e64a0f7dae46b4699c1
Autor:
Büşranur, Çavdarlı, Özlem Yayici, Köken, Saide Betül Arslan, Satılmış, Şule, Bilen, Didem, Ardıçlı, Ahmet Cevdet, Ceylan, Cavidan Nur Semerci, Gündüz, Haluk, Topaloğlu
Publikováno v:
Annals of Human Genetics. 87:104-114
Muscular dystrophies are a heterogeneous group of neuromuscular disorders with a wide range of the clinical and genetic spectrum. Whole-exome sequencing (WES) has been on the rise to become the usual method of choice for molecular diagnosis in patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6adb22957c3e7845807875a0fb20f423
https://doi.org/10.1111/ahg.12492
https://doi.org/10.1111/ahg.12492
Publikováno v:
Turkish Journal of Pediatric Disease. :1-7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0cc145e9de8a7e9cafc1b540104e34f
https://doi.org/10.12956/tchd.974974
https://doi.org/10.12956/tchd.974974
Publikováno v:
Molecular Syndromology. 13:159-164
In this study, we report the first known Turkish case of a novel nonsense mutation c.2453dupT (p.M818fs*28) in the KMT2B (NM_014727.2) gene diagnosed in a male patient with KMT2B-related dystonia (DYT-KMT2B, DYT-28, Dystonia*-28), which is a complex,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98b2af17fb7041091655199b5c54520b
https://doi.org/10.1159/000518974
https://doi.org/10.1159/000518974
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
https://avesis.deu.edu.tr/publication/details/e770a716-7c76-47b6-ae1a-6a20fb66ce13/oai
Autor:
Çağrı Mesut Temuçin, Deniz Yuksel, Ülkühan Öztoprak, Özlem Yayici Köken, Vehap Topcu, Hulya Kayilioglu, Özge Dedeoglu Toptas, Ustun Aydingoz, Busranur Cavdarli
Publikováno v:
Neurology Asia. 26:607-612
Autosomal recessive intermediate Charcot Marie Tooth (CMT) disease type C is a very rarely-seen neurogenetic disorder. Homozygous or compound heterozygous mutation in the Pleckstrin homology domain-containing family G member 5 (PLEKHG5) gene on chrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9be0e356e730a3ce68b2875b0586512d
https://doi.org/10.54029/2021jmr
https://doi.org/10.54029/2021jmr
Autor:
Merve Sibel Güngören, E. Gurkas, Gülsüm İclal Bayhan, Özlem Yayici Köken, Pembe Gultutan, Ayşegül Neşe Çıtak Kurt, Hamit Ozyurek, Deniz Yilmaz
Publikováno v:
Turkish Journal of Medical Sciences
Background/aim This study aimed to analyze the serum melatonin levels and changes in sleep patterns in pediatric patients with coronavirus disease 2019 (COVID-19). Materials and methods This study was designed as a descriptive, cross-sectional study.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0961f775d51513f5c6f89fdbc4a53efb
http://europepmc.org/articles/PMC8569735
http://europepmc.org/articles/PMC8569735