Search Results - "Çelkan, Tiraje"

Hemophagocytic Lymphohistiocytosis by Kaçar, Ayşe Gonca, Celkan, Tiraje Tülin

“…Hemophagocytic lymphohistiocytosis (HLH) is an aggressive life-threatening disease that consists of uncontrolled activated lymphocytes and macrophages that…”
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Impact of having a sibling with cancer or type I diabetes mellitus on psychopathology and self-conscious emotions in adolescents: a comparative study including controls by Erdim, Neşe Kavruk, Koyuncu, Zehra, Keleş, Hüseyin, Durcan, Gizem, Kadak, Muhammed Tayyib, Doğangün, Burak, Celkan, Tiraje

“…Background Objective Having a child diagnosed with cancer is stressful for the whole family and may cause significant psychological impact on parents and…”
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Experience with Pediatric Chronic Immune Thrombocytopenia over 30 Years in the Era before Eltrombopag by Koc, Begum S, Ozdemir, Gul Nihal, Alakbarli, Javid, Apak, Hilmi, Celkan, Tiraje

“…There is limited information on the natural course of chronic ITP in children. We aimed to evaluate the clinical and demographic characteristics of children…”
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Accidental High-dose Intrathecal Treatment: Late Results of a Patient by Celkan, Tiraje, Çifçi Sunamak, Evrim

“…The increase in reporting accidental and overdose use of childhood treatments, starting from 2014, is promising. Understanding the dynamics of overdose may…”
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A Peculiar Disease in a Young Woman Wanting to Get Pregnant by Celkan, Tülin Tiraje, Fenercioğlu, Şeyma, Kaçar, Ayşe Gonca

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Neurofibromatosis Type 1 in Children: A Single-Center Experience by Gonca Kaçar, Ayşe, Kılınc Oktay, Burcu, Çınar Özel, Simge, Ocak, Süheyla, Güneş, Nilay, Uludağ Alkaya, Dilek, Tüysüz, Beyhan, Apak, Hilmi, Tiraje Celkan, Tülin

“…Neurofibromatosis (NF) is the most common autosomal dominantly inherited neurocutaneous syndrome. The characteristic features of NF type 1 (NF-1) are café au…”
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Defective cytotoxic lymphocyte degranulation in syntaxin-11–deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients by Bryceson, Yenan T., Rudd, Eva, Zheng, Chengyun, Edner, Josefine, Ma, Daoxin, Wood, Stephanie M., Bechensteen, Anne Grete, Boelens, Jaap J., Celkan, Tiraje, Farah, Roula A., Hultenby, Kjell, Winiarski, Jacek, Roche, Paul A., Nordenskjöld, Magnus, Henter, Jan-Inge, Long, Eric O., Ljunggren, Hans-Gustaf

“…Familial hemophagocytic lymphohistiocytosis (FHL) is typically an early onset, fatal disease characterized by a sepsislike illness with cytopenia,…”
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Adverse COVID‐19 outcomes in immune deficiencies: Inequality exists between subclasses by Karakoc Aydiner, Elif, Bilgic Eltan, Sevgi, Babayeva, Royale, Aydiner, Omer, Kepenekli, Eda, Kolukisa, Burcu, Sefer, Asena Pinar, Yalcin Gungoren, Ezgi, Karabiber, Esra, Yucel, Esra Ozek, Ozdemir, Oner, Kiykim, Ayca, Artac, Hasibe, Yakici, Nalan, Yalcin, Koray, Cokugras, Haluk, Celkan, Tulin Tiraje, Orhan, Fazil, Yesilipek, Mehmet Akif, Baris, Safa, Ozen, Ahmet

“…Background Genetic deficiencies of immune system, referred to as inborn errors of immunity (IEI), serve as a valuable model to study human immune responses. In…”
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Adrenal masses in children: Imaging, surgical treatment and outcome by Emre, Şenol, Özcan, Rahşan, Bakır, Ayten Ceren, Kuruğoğlu, Sebuh, Çomunoğlu, Nil, Şen, Hilal Susam, Celkan, Tiraje, Tekant, Gonca Topuzlu

“…This study aims to evaluate the current surgical approach to adrenal masses in the pediatric age group. We retrospectively analyzed cases that underwent…”
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An Unusual Presentation of Carney Complex by Dağdeviren Çakır, Aydilek, Turan, Hande, Celkan, Tiraje, Çomunoğlu, Nil, Ercan, Oya, Evliyaoğlu, Olcay

“…Carney complex (CNC) is a multiple neoplasia syndrome, characterized by pigmented lesions of the skin and mucosa, cardiac, cutaneous and other myxomas and…”
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Role of immunohistochemistry in the differential diagnosis of pediatric renal tumors: expression of cyclin d1, beta-catenin , pdgfr-alpha, and pten by Kepil, Nuray, Batur, Cebnem, Kain, Zeynep Ecem, Ozcan, Gamze, Emre, Senol, Ozcan, Rahfan, Celkan, Tulin Tiraje, Comunoglu, Nil

“…Objective: Pediatric renal tumors overlap histomorphologically and may cause misdiagnosis. We aimed to determine the role of immunohistochemical staining of…”
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PTEN and AKT1 Variations in Childhood T-Cell Acute Lymphoblastic Leukemia by Küçükcankurt, Fulya, Erbilgin, Yücel, Fırtına, Sinem, Hatırnaz Ng, Özden, Karakaş, Zeynep, Celkan, Tiraje, Ünüvar, Ayşegül, Özbek, Uğur, Sayitoğlu, Müge

“…PTEN/AKT pathway deregulations have been reported to be associated with treatment response in acute leukemia. This study examined pediatric T-cell acute…”
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Clinical and Molecular Characterization of Fanconi Anemia Patients in Turkey by Toksoy, Güven, Uludağ Alkaya, Dilek, Bagirova, Gülendam, Avcı, Şahin, Aghayev, Agharza, Günes, Nilay, Altunoğlu, Umut, Alanay, Yasemin, Başaran, Seher, Berkay, Ezgi G., Karaman, Birsen, Celkan, Tiraje T., Apak, Hilmi, Kayserili, Hülya, Tüysüz, Beyhan, Uyguner, Zehra O.

“…Fanconi anemia (FA) is a rare multigenic chromosomal instability syndrome that predisposes patients to life-threatening bone marrow failure, congenital…”
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Evolution and long‐term outcomes of combined immunodeficiency due to CARMIL2 deficiency by Kolukisa, Burcu, Baser, Dilek, Akcam, Bengu, Danielson, Jeffrey, Bilgic Eltan, Sevgi, Haliloglu, Yesim, Sefer, Asena Pinar, Babayeva, Royale, Akgun, Gamze, Charbonnier, Louis‐Marie, Schmitz‐Abe, Klaus, Kendir Demirkol, Yasemin, Zhang, Yu, Gonzaga‐Jauregui, Claudia, Jimenez Heredia, Raul, Kasap, Nurhan, Kiykim, Ayca, Ozek Yucel, Esra, Gok, Veysel, Unal, Ekrem, Pac Kisaarslan, Aysenur, Nepesov, Serdar, Baysoy, Gokhan, Onal, Zerrin, Yesil, Gozde, Celkan, Tulin Tiraje, Cokugras, Haluk, Camcioglu, Yildiz, Eken, Ahmet, Boztug, Kaan, Lo, Bernice, Karakoc‐Aydiner, Elif, Su, Helen C., Ozen, Ahmet, Chatila, Talal A., Baris, Safa

“…Background Biallelic loss‐of‐function mutations in CARMIL2 cause combined immunodeficiency associated with dermatitis, inflammatory bowel disease (IBD), and…”
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Association of the TLR4 and NOD2 Polymorphisms with Childhood Acute Lymphoblastic Leukemia by BATAR, Bahadir, MUTLU, Tuba, OZDEMIR, Nihal, CELKAN, Tiraje, GUVEN, Mehmet

“…Objective:Immune activation plays a critical role in the immune response against cancer. Although several genetic factors are established with regard to the…”
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LANGERANS CELL HISTIOCYTOSIS: SINGLE CENTER EXPERIENCE OF 25 YEARS by Tuysuz, Gulen, Yildiz, İnci, Ozdemir, Nihal, Adaletli, Ibrahim, Kurugoglu, Sebuh, Apak, Hilmi, Dervisoglu, Sergulen, Bozkurt, Selen, Celkan, Tiraje

“…Objectives: To review a single center outcome of patients with Langerhans Cell Histiocytosis diagnosed at a referral tertiary hospital from Turkey.Methods: The…”
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Use of a High-Purity Factor X Concentrate in Turkish Subjects with Hereditary Factor X Deficiency: Post Hoc Cohort Subanalysis of a Phase 3 Study by Öner, Ahmet F, Celkan, Tiraje, Timur, Çetin, Norton, Miranda, Kavaklı, Kaan

“…Hereditary factor X (FX) deficiency is a rare bleeding disorder more prevalent in countries with high rates of consanguineous marriage. In a prospective,…”
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Outcomes of Eltrombopag Treatment and Development of Iron Deficiency in Children with Immune Thrombocytopenia in Turkey by Koca Yozgat, Ayça, Leblebisatan, Göksel, Akbayram, Sinan, Çınar Özel, Simge, Karakaş, Zeynep, Erduran, Erol, Yılmaz, Şebnem, Koçak, Ülker, Ünal, Şule, Özdemir, Gül Nihal, Albayrak, Meryem, Zengin, Emine, Oymak, Yeşim, Bör, Özcan, Çakmaklı, Hasan Fatih, Söker, Murat, Gürlek Gökçebay, Dilek, Tokgöz, Hüseyin, Malbora, Barış, Karaman, Serap, Celkan, Tiraje, Şaşmaz, İlgen, Yaralı, Neşe, Ören, Hale, Ünüvar, Ayşegül, Özbek, Namık Yaşar

“…Immune thrombocytopenia (ITP) is a rare autoimmune disease and hematologic disorder characterized by reduced platelet counts that can result in significant…”
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INVESTIGATION OF SALİVARY MIR-9 AND SERUM CIP2A LEVELS IN FANCONI ANEMIA PATIENTS AT HIGH RISK OF DEVELOPING ORAL SQUAMOUS CELL CARCINOMA by Zişan Asal Kılıç, Çetin Timur, Tülin Tiraje Celkan, Şahin Öğreden, Nevin Yalman

“…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…”
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Plasminogen deficiency by Celkan, Tiraje

“…Plasminogen plays an important role in fibrinolysis as well as wound healing, cell migration, tissue modeling and angiogenesis. Congenital plasminogen…”
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