Zobrazeno 1 - 10
of 124
pro vyhledávání: '"Yeşim OYMAK"'
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 12, Iss 1, Pp 76-80 (2022)
Objective: Hemovigilance covers the entire transfusion chain, from the collection of the blood product and its components to the monitoring of adverse reactions. The aim of our study was to perform a process validation for the hemovigilance system of
Externí odkaz:
https://doaj.org/article/2dd8c09869ae4360be19650c313c22be
Autor:
Emine Zengin, Nazan Sarper, Arzu Yazal Erdem, Işık Odaman Al, Melike Sezgin Evim, Neşe Yaralı, Burcu Belen, Arzu Akçay, Ayşen Yıldırım, Tuba Hilkay Karapınar, Adalet Meral Güneş, Sema Aylan Gelen, Hale Ören, Lale Olcay, Birol Baytan, Hüseyin Gülen, Gülyüz Öztürk, Mehmet Fatih Orhan, Yeşim Oymak, Sibel Akpınar, Özlem Tüfekçi, Meryem Albayrak, Burçak Tatlı Güneş, Aylin Canpolat, Namık Özbek
Publikováno v:
Turkish Journal of Hematology, Vol 38, Iss 4, Pp 294-305 (2021)
Objective: This study aimed to evaluate systemic thrombolysis experiences with recombinant tissue plasminogen activator (rtPA). Materials and Methods: Retrospective data were collected from 13 Turkish pediatric hematology centers. The dose and durati
Externí odkaz:
https://doaj.org/article/e6651da5e2b34eb7b892f7bbb80c64ac
Autor:
Işık Odaman Al, Yeşim Oymak, Tuba Hilkay Karapınar, Melek Erdem, Salih Gözmen, Neryal Tahta, Sultan Okur Acar, ilknur Çağlar, Nuri Bayram, İlker Devrim
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 11, Iss 2, Pp 181-187 (2021)
Objective: Infections are an important cause of morbidity and mortality for patients with congenital neutropenia. In the present study, we report on the incidence, type, localization of documented infections, as well as the clinical features and long
Externí odkaz:
https://doaj.org/article/a67249bceb5347f597e442b1f2244967
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
Autor:
Tahir Atik, Esra Işık, Hüseyin Onay, Bilçağ Akgün, Moharram Shamsali, Kaan Kavaklo, Melike Evim, Gülen Tüysüz, Namık Yaşar Özbek, Fahri Şahin, Zafer Salcıoğlu, Canan Albayrak, Yeşim Oymak, Ekrem Ünal, Fatma Burcu Belen, Ebru Yılmaz Keskin, Can Balkan, Birol Baytan, Alphan Küpesiz, Vildan Culha, Tuba Nur Tahtakesen, Adalet Meral Güneş, Ferda Özkınay
Publikováno v:
Turkish Journal of Hematology, Vol 37, Iss 3, Pp 145-153 (2020)
Objective: Hemophilia A (HA) is the most severe X-linked inherited bleeding disorder caused by hemizygous mutations in the factor 8 (F8) gene. The aim of this study is to determine the mutation spectrum of the F8 gene in a large HA cohort from Turkey
Externí odkaz:
https://doaj.org/article/739b1796010f4465a28442c9b6243a1b
Autor:
Ayşegül Ünüvar, Serap Karaman, Deniz Tuğcu, Melike Sezgin Evim, Arzu Akçay, İbrahim Eker, Funda Tayfun Küpesiz, Namık Özbek, Mehmet Ertem, Sultan Aydın, Zuhal Keskin, Yusuf Ziya Aral, Zülfükar Gördü, Murat Elli, Ayşe Özkan Karagenç, Burcu Belen Apak, Hülya Uzel, Murat Söker, Tuba Karapınar, Yeşim Oymak, Nihal Karadaş, Alper Özcan, Ersin Töret, Ülker Koçak, Sinan Akbayram, Şule Ünal Cangül, Aylin Canbolat Ayhan, Tiraje Celkan, Bülent Zülfikar, Rejin Kebudi, Şadan Hacısalihoğlu, Erol Erduran, Sema Aylan Gelen, Nazan Sarper, Fatih Erbey, Emin Kürekçi, Hüseyin Gülen, Barış Yılmaz, Ömer Doğru, Ahmet Koç, Selma Ünal, Hüseyin Tokgöz, Canan Albayrak, Yılmaz Ay, Fatih Orhan, Davut Albayrak, Neslihan Karakurt, Betül Orhaner, Emine Türkkan, Yıldız Yıldırmak, Hadi Geylani, Begüm Koç, Ahmet Fayik Öner, Çetin Timur, Hale Ören
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S55-S56 (2021)
Objective: A questionnaire form was prepared by the Turkish Pediatric Hematology Society- Subcommittee of Hemostasis, Thrombosis and Hemophilia to determine the current approaches in the diagnosis and treatment of childhood ITP in our country. Our ai
Externí odkaz:
https://doaj.org/article/0eb80f230816404ab892c71ef0fed017
Autor:
İlknur Çağlar, İlker Devrim, Özgür Cartı, Mine Duzgol, Ahu Kara Aksay, Bengü Demirag, Salih Gözmen, Yılmaz Ay, Tuba Hilkay Karapınar, Nuri Bayram, Yeşim Oymak, Canan Vergin
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 9, Iss 3, Pp 239-244 (2019)
INTRODUCTION: There are limited data focusing on cytomegalovirus (CMV) incidence and manifestations in children with acute lymphoblastic leukemia (ALL) apart from bone marrow transplant recipients. In this study, we review our experience of the manif
Externí odkaz:
https://doaj.org/article/5c9277fda9a24004bf9f22cdf626349d
Publikováno v:
Journal of Pediatric Research, Vol 6, Iss 3, Pp 252-255 (2019)
Type II Griscelli Syndrome (GS) is caused by a mutation in the RAB27A gene and usually manifests with silvery-gray hair, immune deficiency and the development of hemophagocytic lymphohistiocytosis (HLH). A hematopoietic stem cell transplantation is t
Externí odkaz:
https://doaj.org/article/36a296fc089b407a8e9f9d09acb9cb96
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 9, Iss 2, Pp 160-163 (2019)
INTRODUCTION: Compliance to treatment regimens is a current issue in the treatment of hemophilia. These problems are widely reported. We aimed to investigate the effect of self-infusion and patient education on treatment compliance in hemophilia pati
Externí odkaz:
https://doaj.org/article/220c6f57b7ba4353988ea8100bba2b64
Autor:
Yöntem Yaman, Sultan Aydin Köker, Fahri Yüce Ayhan, Ferah Genel, Can Acıpayam, Yeşim Oymak, Ebru Tuğrul Sarıbeyoğlu, Canan Raziye Vergin
Publikováno v:
Central European Journal of Immunology, Vol 44, Iss 2, Pp 206-209 (2019)
Leukocyte adhesion deficiency type II (LAD II) is a rare, autosomal, recessive inherited immunodeficiency disease that induces frequent and recurrent infections, persistent leukocytosis, severe mental and growth retardation, and impaired wound healin
Externí odkaz:
https://doaj.org/article/898ed3f8357a42869f007c3fb314c9e8