Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Eren Arslan Davulcu"'
Autor:
Zehra Narlı Özdemir, Yıldız İpek, Püsem Patır, Gözde Ermiş, Rafiye Çiftçiler, Deniz Özmen, Mehmet Baysal, Vildan Gürsoy, Esra Yıldızhan, Serkan Güven, Tarık Ercan, Tayfun Elibol, Sinan Mersin, Eylem Genç, Eren Arslan Davulcu, Volkan Karakuş, Nergiz Erkut, Gürsel Güneş, Reyhan Diz Küçükkaya, Ahmet Emre Eşkazan
Publikováno v:
Turkish Journal of Hematology, Vol 41, Iss 1, Pp 26-36 (2024)
Objective: In this study, we investigated the effects of calreticulin (CALR) and JAK2V617F mutational status on clinical course and disease outcomes in Turkish patients with essential thrombocythemia (ET). Materials and Methods: Seventeen centers fr
Externí odkaz:
https://doaj.org/article/ab5f757b27aa42b59fc159ec0b70c9e6
Autor:
Eren Arslan Davulcu, Tarık Onur Tiryaki, Elif Aksoy, Emine Gültürk, İpek Yönal Hindilerden, Meliha Nalçacı, Fehmi Hindilerden
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S39-S40 (2023)
Objective: Autoimmune hemolytic anemias (AIHA) are rare disorders where autoantibodies destroy self-red blood cells. AIHA includes warm AIHA (wAIHA), cold AIHA (cAIHA or cold agglutinin disease), mixed AIHA (mAIHA), paroxysmal cold hemoglobinuria (PC
Externí odkaz:
https://doaj.org/article/0edee5796bdc4344843d84c23bd75bdf
Autor:
Anıl Tombak, Funda Pepedil Tanrıkulu, Salih Sertaç Durusoy, Hüseyin Derya Dinçyürek, Emin Kaya, Elif Gülsüm Ümit, İrfan Yavaşoğlu, Özgür Mehtap, Burak Deveci, Mehmet Ali Özcan, Hatice Terzi, Müfide Okay, Nilgün Sayınalp, Mehmet Yılmaz, Vahap Okan, Alperen Kızıklı, Ömer Özcan, Güven Çetin, Sinan Demircioğlu, İsmet Aydoğdu, Güray Saydam, Eren Arslan Davulcu, Gül İlhan, Mehmet Ali Uçar, Gülsüm Özet, Seval Akpınar, Burhan Turgut, İlhami Berber, Erdal Kurtoğlu, Mehmet Sönmez, Derya Selim Batur, Rahşan Yıldırım, Vildan Özkocaman, Ahmet Kürşad Güneş, Birsen Sahip, Şehmus Ertop, Olga Meltem Akay, Abdülkadir Baştürk, Mehmet Hilmi Doğu, Aydan Akdeniz, Ali Ünal, Ahmet Seyhanlı, Emel Gürkan, Demet Çekdemir, Burhan Ferhanoğlu
Publikováno v:
Turkish Journal of Hematology, Vol 38, Iss 4, Pp 273-285 (2021)
Objective: This study aimed to retrospectively evaluate the efficacy, safety, and survival outcome of single-agent ibrutinib therapy in chronic lymphocytic leukemia patients. Materials and Methods: A total of 136 patients (mean age +- standard deviat
Externí odkaz:
https://doaj.org/article/506b9a34c2d64dd5beb096f766347808
Publikováno v:
Turkish Journal of Hematology, Vol 37, Iss 4, Pp 304-306 (2020)
Externí odkaz:
https://doaj.org/article/f0e9b6e4036546878f09a90894c41803
Publikováno v:
Ege Tıp Dergisi. :119-124
Aim: The aim of the study was to investigate whether multimorbidities, comorbidities, and therefore polypharmacy increase with age in hemophilia A and B patients followed in Ege University Adult Hemophilia and Thrombosis Center. Materials and Methods
Autor:
Eren Arslan Davulcu, Nur Soyer, Zühal Demirci, Ajda Güneş, Filiz Vural, Fahri Şahin, Mahmut Töbü, Serra Kamer, Mine Hekimgil, Güray Saydam
Publikováno v:
Clinical Hematology International.
Purpose Langerhans cell histiocytosis (LCH) is a rare disease that can affect all tissues and organs. Our study evaluated the clinical characteristics and treatment outcomes of adult-onset LCH patients in a tertiary center. Materials and Methods Adul
Autor:
Başak Doğanavşargil, Mahmut Töbü, Emre Demir, Derya Demir, Ayşenur Arslan, Güray Saydam, Nur Soyer, Mine Hekimgil, Nazan Özsan, Eren Arslan Davulcu
Publikováno v:
Ege Tıp Dergisi
Aim: Non-Hodgkin's lymphomas (NHL) are a heterogeneous group of lymphoproliferative diseases. The aim of this study was to evaluate the epidemiological analysis of NHL patients and compare them to global findings.Materials and Methods: The data inclu
Autor:
Eren Arslan Davulcu, Mert Pekerbas, Emin Karaca, Burak Durmaz, Nazan Özsan, Haluk Akın, Güray Saydam
Chronic myeloid leukemia (CML) is a common hematological malignancy originating from bone marrow stem cells. Chromosomal abnormalities can be seen in almost all cases, the most known anomaly being Philadelphia (Ph) chromosome, a derivative chromosome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d04cc5fea742ad6b61a2305e35571c7
https://hdl.handle.net/11454/76443
https://hdl.handle.net/11454/76443
Autor:
Eren Arslan Davulcu, Zühal Demirci, Umut Yılmaz, Muhlis Cem Ar, Hava Üsküdar Teke, Volkan Karakuş, Rafiye Çiftçiler, Cem Selim, İrfan Yavaşoğlu, Salih Sertaç Durusoy, Vahap Okan, Aydan Akdeniz, Alkım Yolcu, İsmet Aydoğdu, Tekin Güney, Asu Fergün Yılmaz, Fahri Şahin
Acquired hemophilia A (AHA) is a rare disease caused by autoantibodies inhibiting factor VIII (FVIII) activity. Although the conditionis usually idiopathic, there may be other underlying diseases. Treatment consists of two steps: treatment of acute b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::744f6e5495a4b4fba10e552e50e10563
https://hdl.handle.net/11454/76288
https://hdl.handle.net/11454/76288
Publikováno v:
Turkiye Klinikleri Journal of Case Reports. 27:221-225
HHV-8 is associated with Kaposi sarcoma, multicentric Castleman disease and primary effusion lymphoma mostly in immunocompromised patients. in this report, we describe a female patient without any immunosuppressive state, encountering those three mal