Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Murat Muhtar Yılmaz"'
Autor:
Mustafa Mertkan Bilen, Murat Muhtar Yılmazer, Gamze Vuran, Mehmet Murat, Ceren Karahan, Cem Doğan, Yusuf İlker Dur, Timur Meşe
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 14, Iss 2, Pp 71-80 (2024)
Objective: Transcatheter closure of patent ductus arteriosus (PDA) has taken its place as the first choice in the treatment of PDA thanks to the development of new devices and techniques. In this study, we present our cases with PDA closed with Ampla
Externí odkaz:
https://doaj.org/article/4842c7b0c4f64171948e3b83329362af
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 14, Iss 2, Pp 91-96 (2024)
Objective: This study aims to evaluate right atrial functions in children with pulmonary arterial hypertension (PAH) associated with congenital heart disease (CHD) by deformation indices assessed by two dimensional-speckle tracking echocardiography.
Externí odkaz:
https://doaj.org/article/1d56f8a6efad48e097d1beb6cd7c3f49
Autor:
Mustafa Mertkan Bilen, Timur Meşe, Murat Muhtar Yılmazer, Ceren Karahan, Mehmet Murat, Gamze Vuran, Cem Doğan
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 14, Iss 1, Pp 10-14 (2024)
Objective: This study investigates electrocardiographic (ECG) findings in pediatric patients diagnosed with Multisystem Inflammatory Syndrome in Children (MIS-C) during the coronavirus disease-2019 pandemic, offering valuable insights into the diagno
Externí odkaz:
https://doaj.org/article/30e4ed71250e4f1e803093d21b7a6450
Autor:
Selvinaz Edizer, Engin Kose, Aycan Ünalp, Hüseyin Onay, Ünsal Yılmaz, Murat Muhtar Yılmaz, Timur Meşe, Melis Köse, Eser Sozmen Yildirim, Semra Gürsoy, Mehtap Kagnici
Introduction: Pompe disease (PD), glycogen storage disease Type II (GSD II), is an autosomal recessive inherited lysosomal storage disease caused by pathogenic variants in the GAA gene that encodes lysosomal acid ?-glucosidadase (GAA) enzyme. the inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e65899b29aade856229c92c52a166b49
https://avesis.deu.edu.tr/publication/details/17405ad8-3eb0-416a-9cb5-990c9ef0dac8/oai
https://avesis.deu.edu.tr/publication/details/17405ad8-3eb0-416a-9cb5-990c9ef0dac8/oai
Publikováno v:
Bakirkoy Tip Dergisi / Medical Journal of Bakirkoy. :178-181
Objective: Herpes zoster (HZ) occurs due to reactivation of the latent varicella zoster virus and is rare in childhood. HZ is believed to be rare, frequently mild and postzoster neuralgia rarely if ever occurs. The aim of this retrospective study was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e02e1947b18b8517d4a3c122a362948
https://doi.org/10.5350/btdmjb201208405
https://doi.org/10.5350/btdmjb201208405
Autor:
Alper Sevimli, Mehmet Karadag, Arzu Yilmaztepe, Asuman Tokullugil, Melike Koç, B. Bahadir Erdogan, Berrin Zik, Semra Akgöz, Murat Muhtar Yılmaz, A. Yagci, Engin Ulukaya
Publikováno v:
Cancer Investigation. 25:322-327
Tumor growth and metastasis depend on angiogenesis, and the vascular endothelial growth factor (VEGF) is known to be one of the most important angiogenic factors although the knowledge about its receptors is limited. We, therefore, investigated the t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a156b02d1e82cbe0c67dbe6b90f7248e
https://doi.org/10.1080/07357900701209178
https://doi.org/10.1080/07357900701209178
Autor:
Semra Gürsoy, Filiz Hazan, Cüneyt Zihni, Sezer Acar, Murat Muhtar Yılmazer, Timur Meşe, Behzat Özkan
Publikováno v:
Journal of Pediatric Research, Vol 8, Iss 3, Pp 297-302 (2021)
Aim:Williams-Beuren syndrome, which is characterized by dysmorphic facial features, cardiovascular findings, intellectual disability, endocrine abnormalities and a typical cognitive profile, is caused by a microdeletion in the 7q11.23 region. In this
Externí odkaz:
https://doaj.org/article/56a7e3460ec04a8a8563d29e7c9dd628
Autor:
Nagehan Katipoğlu, Mehmet Küçük, Timur Meşe, Rahmi Özdemir, Murat Muhtar Yılmazer, Utku Karaarslan
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 9, Iss 1, Pp 34-40 (2019)
INTRODUCTION: Pulmonary valve stenosis is the most common of the right ventricular outflow tract obstruction, BVP has been the treatment of choice in these subgroup of patients. In this study, we aimed to evaluate right ventricular functions of patie
Externí odkaz:
https://doaj.org/article/871b98f2edbd4aad99ea44911c66e04b
Autor:
Eser Doğan, Mustafa Karaçelik, Murat Muhtar Yılmazer, Timur Meşe, Çağatay Bilen, Cüneyt Zihni, Engin Gerçeker, Gamze Vuran, Mehmet Murat, Ceren Karahan
Publikováno v:
Anatolian Journal of Cardiology, Vol 25, Iss 10, Pp 743-744 (2021)
Externí odkaz:
https://doaj.org/article/6451d18275674f0380bd5a0dec99bfcb
Autor:
Taliha Oner, Rahmi Ozdemir, Dildar Bahar Genc, Mehmet Kucuk, Cem Karadeniz, Savas Demirpence, Murat Muhtar Yilmazer, Timur Mese, Vedide Tavli, Ferah Genel
Publikováno v:
Jornal de Pediatria (Versão em Português), Vol 92, Iss 6, Pp 581-587 (2016)
Objective: The aim of this study is to define the predictors of chronic carditis in patients with acute rheumatic carditis (ARC). Methods: Patients diagnosed with ARC between May 2010 and May 2011 were included in the study. Echocardiography, electro
Externí odkaz:
https://doaj.org/article/35b556fd81a9476bb1af26e96fe74c59