Zobrazeno 1 - 10
of 139
pro vyhledávání: '"Serap Karaman"'
Autor:
Rustu Oguz, Hayriye Senturk Ciftci, Muge Gokce, Yeliz Ogret, Sedat Karadeniz, Sacide Pehlivan, Kursat Ozdilli, Zeynep Karakas, Serap Karaman, Filiz Aydın
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss 4, Pp 327-334 (2024)
Introduction: Epidemiologic studies on pediatric acute lymphoblastic leukemias (ALL) have been conducted to evaluate the possible risk factors including genetic, infectious and environmental factors with the objective of idenfying the etiology. Manno
Externí odkaz:
https://doaj.org/article/b1176e35743548c0b020e195cf7ef689
Autor:
Nur Aycan, Eyyüp Yürektürk, Ali Ateş, Kemal Ayengin, Emel Nadya Toplar, Serap Karaman, Oğuz Tuncer
Publikováno v:
Bagcilar Medical Bulletin, Vol 8, Iss 2, Pp 194-197 (2023)
Umbilical anomalies are seen quite frequently in the neonatal period. Knowing the embryological development steps and anatomy is essential for accurate diagnosis and treatment in cases with umbilical pathology. A rare type of these anomalies is the p
Externí odkaz:
https://doaj.org/article/cea30ee2931d478f812a769dc2159004
Autor:
Deniz Tugcu, Leyla Valıyeva, Sifa Sahın, Rumeysa Tuna, Mustafa Bılıcı, Ayşegül Unuvar, Serap Karaman, Gülşah Tanyıldız, Selda Hancerli, Sevim Mese, Ali Agacfıdan, Ayper Somer, Zeynep Karakas
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S29- (2023)
Objective: Respiratory viruses are an important cause of morbidity and mortality in pediatric hematology oncology patients. We aimed to determine the infection rate, clinical and epidemiological characteristics of respiratory viruses in pediatric pat
Externí odkaz:
https://doaj.org/article/a5ac561e39a84f96a97da1c4a21f9fff
Autor:
Melda Berber Hamamcı, Şule Yeşil, Firdevs Aydın, Gülcan Erbaş, Deniz Tuğcu, Şifa Şahin, Zuhal Bayramoğlu, Yasin Ateş, Serap Karaman, Hikmet Gülşah Yıldız, Hakan Kocaman, Elif Dede, Ayper Somer, Ayşegül Ünüvar, Zeynep Karakaş
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S46-S47 (2023)
Case report: The 22-month-old male and 15-day-old female patients presented with persistent stridor since birth. Tracheoscopy of the first patient revealed a 90% obstructing hemangioma in the subglottic area, while the second patient's CT scan showed
Externí odkaz:
https://doaj.org/article/a72efa10807e48008a63c0fe551f4dc2
Autor:
Şifa Şahin, Serap Karaman, Yasin Yılmaz, Mustafa Bilici, Saadet Aslan, Hikmet Gülşah Tanyıldız, Deniz Tuğcu, Zeynep Karakaş, Ayşegül Ünüvar
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S21-S22 (2022)
Objective: It is known that there were transportation problems to the hospital and treatment experienced in many disease groups during the pandemic process. The negative impact of the pandemic is particularly evident in chronic diseases and in situat
Externí odkaz:
https://doaj.org/article/303e82360c2a4b31a26bbff631e8ec50
Autor:
Serap Karaman, Şifa Şahin, Edibe Pembegül Yıldız, Hikmet Gülşah Tanyıldız, Mehmet Barburoğlu, Tutku Turgut, Yasin Yılmaz, Zeynep Karakaş, Deniz Tuğcu, Ayşegül Ünüvar
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S43- (2022)
Introduction: Neurofibromatosis type 1 (NF-1) is the most prevalent autosomal dominant genetic disorder. NF-1 vasculopathy is a significant complication of the disease. It affects both arterial and venous blood vessels of all sizes. Also Moyamoya syn
Externí odkaz:
https://doaj.org/article/b07cf4caf4d54ed5be7db4a2086bdcb2
Autor:
Aysegul Unuvar, Levent Aydemir, Mehmet Barburoglu, Sifa Sahin, Mustafa Bilici, Deniz Tugcu, Gulsah Tanyildiz, Zeynep Karakas, Serap Karaman
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S38- (2022)
Objective: The bleeding phenotype of patients with inherited FVII deficiency is variable, and epistaxis is one of the most frequent symptoms. Interestingly, the bleeding risk does not correlate with the level of FVII activity. The severity of FVII de
Externí odkaz:
https://doaj.org/article/053327ea2a074902baa51921d11d0d93
Autor:
Serap Karaman, Eda Çelebi Bitkin
Publikováno v:
Van Tıp Dergisi, Vol 28, Iss 2, Pp 211-214 (2021)
INTRODUCTION: In this study, we aimed to investigate the effects of chemotherapy and radiotherapy on thyroid functions in cases where chemotherapy and radiotherapy were given in our pediatric hematology unit and the treatment resulted in healing, and
Externí odkaz:
https://doaj.org/article/3861d378a5894e3c8fbb3d2622b7415c
Autor:
Kamuran Karaman, Eyüp Yürektürk, Hadi Geylan, Akkız Şahin Yaşar, Serap Karaman, Huri Sema Aymelek, Mecnun Çetin, Ahmet Fayik Oner
Publikováno v:
Platelets, Vol 32, Iss 2, Pp 238-242 (2021)
Glanzmann’s thrombasthenia (GT) is an autosomal recessive disorder in which the underlying problem is the lack or dysfunction of the GpIIb/IIIa receptor on the platelet surface. The present study determines the genetic mutation typology and analyze
Externí odkaz:
https://doaj.org/article/fd04d405f9504f739929fde27b30e2fe
Autor:
Ayça Koca Yozgat, Göksel Leblebisatan, Sinan Akbayram, Simge Çınar Özel, Zeynep Karakaş, Erol Erduran, Şebnem Yılmaz, Ülker Koçak, Şule Ünal, Gül Nihal Özdemir, Meryem Albayrak, Emine Zengin, Yeşim Oymak, Özcan Bör, Hasan Fatih Çakmaklı, Murat Söker, Dilek Gürlek Gökçebay, Hüseyin Tokgöz, Barış Malbora, Serap Karaman, Tiraje Celkan, İlgen Şaşmaz, Neşe Yaralı, Hale Ören, Ayşegül Ünüvar
Publikováno v:
Turkish Journal of Hematology, Vol 37, Iss 3, Pp 139-144 (2020)
Objective: Immune thrombocytopenia (ITP) is a rare autoimmune disease and hematologic disorder characterized by reduced platelet counts that can result in significant symptoms, such as bleeding, bruising, epistaxis, or petechiae. The thrombopoietin r
Externí odkaz:
https://doaj.org/article/0659ce0b12024b1d800b0a65ac28cbd5