Zobrazeno 1 - 10
of 230
pro vyhledávání: '"Tiraje Celkan"'
Publikováno v:
Children, Vol 11, Iss 9, p 1051 (2024)
Background: There is limited information on the natural course of chronic ITP in children. We aimed to evaluate the clinical and demographic characteristics of children with chronic ITP in the era before the availability of eltrombopag. Methods: A to
Externí odkaz:
https://doaj.org/article/e7d90e634c984c888d816b92a86fec5e
Autor:
Eren Gündüz, Hakkı Onur Kırkızlar, Elif Gülsüm Ümit, Sedanur Karaman Gülsaran, Vildan Özkocaman, Fahir Özkalemkaş, Ömer Candar, Tugrul Elverdi, Selin Küçükyurt, Semra Paydaş, Özcan Çeneli, Sema Karakuş, Senem Maral, Ömer Ekinci, Yıldız İpek, Cem Kis, Zeynep Tuğba Güven, Aydan Akdeniz, Tiraje Celkan, Ayşe Hilal Eroğlu Küçükdiler, Gülsüm Akgün Çağlıyan, Ceyda Özçelik Şengöz, Ayşe Karataş, Tuba Bulduk, Alper Özcan, Fatma Burcu Belen Apak, Aylin Canbolat, İbrahim Kartal, Hale Ören, Ersin Töret, Gül Nihal Özdemir, Şule Mine Bakanay Öztürk
Publikováno v:
Turkish Journal of Hematology, Vol 39, Iss 2, Pp 130-135 (2022)
Objective: Castleman disease (CD) is a rare disease also known as angiofollicular lymph node hyperplasia. The two main histological subtypes are the hyaline vascular and plasma cell variants. It is further classified as unicentric CD (UCD) or multice
Externí odkaz:
https://doaj.org/article/90602ce9f9bf437588736f9a063da92f
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:
Fulya Küçükcankurt, Yücel Erbilgin, Sinem Fırtına, Özden Hatırnaz Ng, Zeynep Karakaş, Tiraje Celkan, Ayşegül Ünüvar, Uğur Özbek, Müge Sayitoğlu
Publikováno v:
Turkish Journal of Hematology, Vol 37, Iss 2, Pp 98-103 (2020)
Objective: PTEN/AKT pathway deregulations have been reported to be associated with treatment response in acute leukemia. This study examined pediatric T-cell acute lymphoblastic leukemia (T-ALL) samples for PTEN and AKT1 gene variations and evaluated
Externí odkaz:
https://doaj.org/article/9954fe1b2df94d17b048a02166ab52d9
Autor:
Aydilek Dağdeviren Çakır, Hande Turan, Tiraje Celkan, Nil Çomunoğlu, Oya Ercan, Olcay Evliyaoğlu
Publikováno v:
JCRPE, Vol 12, Iss 1, Pp 117-121 (2020)
Carney complex (CNC) is a multiple neoplasia syndrome, characterized by pigmented lesions of the skin and mucosa, cardiac, cutaneous and other myxomas and multiple endocrine and non-endocrine tumors. Most of the cases have an inactivating mutation in
Externí odkaz:
https://doaj.org/article/95d43de1334f4a97a7e53495ba81d61b
Autor:
Şenol Emre, Rahşan Özcan, Ayten Ceren Bakır, Sebuh Kuruğoğlu, Nil Çomunoğlu, Hilal Susam Şen, Tiraje Celkan, Gonca Topuzlu Tekant
Publikováno v:
Asian Journal of Surgery, Vol 43, Iss 1, Pp 207-212 (2020)
Background/objective: This study aims to evaluate the current surgical approach to adrenal masses in the pediatric age group. Methods: We retrospectively analyzed cases that underwent surgery for adrenal masses between 2007 and 2017. Patients were as
Externí odkaz:
https://doaj.org/article/11a85f1397a04e07a8886cff5f760fd8
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
Publikováno v:
Turkish Journal of Hematology, Vol 35, Iss 2, Pp 129-133 (2018)
Hereditary factor X (FX) deficiency is a rare bleeding disorder more prevalent in countries with high rates of consanguineous marriage. In a prospective, open-label, multicenter phase 3 study, 25 IU/kg plasmaderived factor X (pdFX) was administered a
Externí odkaz:
https://doaj.org/article/a988b5d4a362496d8d6b42975259df9b
Publikováno v:
Bezmiâlem Science, Vol 6, Iss 2, Pp 119-125 (2018)
Objective:Immune activation plays a critical role in the immune response against cancer. Although several genetic factors are established with regard to the development of acute lymphoblastic leukemia (ALL), the role of immunogenic genes in ALL patho
Externí odkaz:
https://doaj.org/article/0f94dfa446ac48f8a5d387dbd7b5662d
Autor:
Özlem Tüfekçi, Ülker Koçak, Zühre Kaya, İdil Yenicesu, Canan Albayrak, Davut Albayrak, Şebnem Yılmaz Bengoa, Türkan Patıroğlu, Musa Karakükçü, Ekrem Ünal, Elif Ünal İnce, Tali İleri, Mehmet Ertem, Tiraje Celkan, Gül Nihal Özdemir, Nazan Sarper, Dilek Kaçar, Neşe Yaralı, Namık Yaşar Özbek, Alphan Küpesiz, Tuba Karapınar, Canan Vergin, Ümran Çalışkan, Hüseyin Tokgöz, Melike Sezgin Evim, Birol Baytan, Adalet Meral Güneş, Deniz Yılmaz Karapınar, Serap Karaman, Vedat Uygun, Gülsun Karasu, Mehmet Akif Yeşilipek, Ahmet Koç, Erol Erduran, Berna Atabay, Haldun Öniz, Hale Ören
Publikováno v:
Turkish Journal of Hematology, Vol 35, Iss 1, Pp 27-34 (2018)
Objective: This study aimed to define the status of juvenile myelomonocytic leukemia (JMML) patients in Turkey in terms of time of diagnosis, clinical characteristics, mutational studies, clinical course, and treatment strategies. Materials and Metho
Externí odkaz:
https://doaj.org/article/654e607208ed46828d61d788a67ece8e