Zobrazeno 1 - 10
of 443
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
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S26- (2023)
Objective: Fanconi anemia (FA) is a rare bone marrow failure syndrome caused by mutations in DNA repair genes, and the risk of developing Oral Squamous Cell Carcinoma (OSCC) in FA patients is higher than in the normal population and is seen at younge
Externí odkaz:
https://doaj.org/article/80cebde18baf40a1b4d56aa026bf0725
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:
Nuray KEPIL, Şebnem BATUR, Zeynep Ecem KAIN, Gamze ÖZCAN, Şenol EMRE, Rahşan ÖZCAN, Tülin Tiraje CELKAN, Nil ÇOMUNOĞLU
Publikováno v:
Türk Patoloji Dergisi, Vol 38, Iss 2, Pp 083-089 (2022)
Objective: Pediatric renal tumors overlap histomorphologically and may cause misdiagnosis. We aimed to determine the role of immunohistochemical staining of Cyclin D1, PTEN, beta-catenin and PDGFR-alpha on pediatric renal tumors. Material and Method:
Externí odkaz:
https://doaj.org/article/fc7833df9520451b84e02b72a2cb939c
Publikováno v:
Van Tıp Dergisi, Vol 29, Iss 1, Pp 27-35 (2022)
INTRODUCTION: Relapse is not common in patients with acute leukemia in childhood, however it is a serious complication with high mortality rate. We aimed to predict relapse among pediatric acute leukemia patients in remission by using complete blood
Externí odkaz:
https://doaj.org/article/4b622e6d391b42648a0f02746a37d478
Publikováno v:
Adli Tıp Bülteni, Vol 26, Iss 3, Pp 205-209 (2021)
Neonatal encephalopathy is a clinical picture with convulsion, respiratory depression and hypotonia “appeared” in babies born at 35 weeks and after the first month. The clinical picture detected in the cases varies. When hypoxic ischemic encephal
Externí odkaz:
https://doaj.org/article/359af64854ba4e1c8967e2dc7b5e2531
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