Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Ömer, Ekinci"'
Autor:
İstemi Serin, Mehmet Hilmi Doğu, Ömer Ekinci, Gülsüm Akgün Çağlıyan, Abdulkadir Baştürk, Merih Reis Aras, Sinan Demircioğlu, Burhan Turgut, Mustafa Merter, Sibel Kabukçu Hacıoğlu, Metin Bağcı, Murat Albayrak, Serdal Korkmaz, Mehmet Ali Erkurt, Mehmet Sinan Dal, Fadime Ersoy Dursun, Anıl Tombak, İsmet Aydoğdu, Turgay Ulaş, Fevzi Altuntaş
Publikováno v:
İstanbul Medical Journal, Vol 24, Iss 2, Pp 120-125 (2023)
Introduction:Ruxolitinib is a small -molecule inhibitor of the JAK1/2 pathway. This study aimed to reveal the results and side-effect profile of the use of ruxolitinib as a treatment option in polycythemia vera (PV).Methods:A total of 34 patients wit
Externí odkaz:
https://doaj.org/article/2f9813f1062246cfa7c5bb2a592ed5f8
Prognostic Significance of Flow Cytometric Immunophenotyping in Patients with Acute Myeloid Leukemia
Publikováno v:
Bezmiâlem Science, Vol 10, Iss 4, Pp 402-408 (2022)
Objective:Chromosomal abnormalities are one of the most important prognostic factors in acute myeloid leukemia (AML). However, not all patients may have such informative chromosomal abnormalities. Although there are many studies on the prognostic val
Externí odkaz:
https://doaj.org/article/6216e4967c524ad7bc6db8917f8320da
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:
Ömer Ekinci, Senar Ebinç
Publikováno v:
Van Tıp Dergisi, Vol 27, Iss 3, Pp 287-291 (2020)
INTRODUCTION: We aimed to present the pregnant patients who were consulted with hematologists for microangiopathic hemolytic anemia and/or thrombocytopenia and were diagnosed HELLP syndrome. METHODS: A total of 32 patients, who were diagnosed with HE
Externí odkaz:
https://doaj.org/article/ec26d0d44eef4015a1ef7ba35b14d95d
Publikováno v:
Cukurova Medical Journal, Vol 45, Iss 2, Pp 533-540 (2020)
Amaç: Bu çalışmada non-Hodgkin lenfoma (NHL) hastalarının epidemiyolojik, demografik, klinik ve prognostik özelliklerini araştırmayı amaçladık. Gereç ve Yöntem: İnönü Üniversitesi Tıp Fakültesi Hematoloji kliniğinde 2000 ile 2016
Externí odkaz:
https://doaj.org/article/0deefbc555744a9db5baf8a88c570951
Publikováno v:
Van Tıp Dergisi, Vol 26, Iss 3, Pp 337-341 (2019)
INTRODUCTION: Extramedullary myeloma (EMM) is defined by the presence of plasma cells outside the bone marrow in a patient with multiple myeloma (MM). More using sensitive imaging techniques, EMM may be found in up to 30% of MM patients across the ov
Externí odkaz:
https://doaj.org/article/8633d8680c974e31bbec698d39d24de9
Autor:
Sinan Demircioğlu, Ali Doğan, Ömer Ekinci, Ufuk Düzenli, Ali İrfan Baran, İrfan Bayram, Cengiz Demir
Publikováno v:
Van Tıp Dergisi, Vol 26, Iss 1, Pp 120-124 (2019)
Mucormycosis is a rare, emerging fungal infection, with high morbidity and mortality. Rhino-orbito-cerebral form is common. In the treatment of this form, it is recommended to apply amphotericin B and surgery together. However, despite these treatmen
Externí odkaz:
https://doaj.org/article/ee8aab986d5e458eba990d97dda26661
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 42, Iss , Pp 17- (2020)
Externí odkaz:
https://doaj.org/article/a2cc8636a4114f32be999981eb4962d7
Publikováno v:
Van Tıp Dergisi, Vol 24, Iss 4, Pp 378-381 (2017)
Rheumatoid arthritis (RA) is a systemic inflammatory disease whose etiology is not fully known and is characterised by destruction of synovial membrane which is caused by inflammation in the joints and synovial cell proliferation. Methotrexate (MTX)
Externí odkaz:
https://doaj.org/article/ce14da8fe96948a49478b76f20a151da
Autor:
Ali Doğan, Narin Yıldırım Doğan, Ömer Ekinci, Sinan Demircioğlu, Cengiz Demir, Cihan Ural, Ramazan Esen
Publikováno v:
Journal of Current Hematology & Oncology Research. 1:15-17
Hemolytic anemia is characterized by a decrease in the number of circulating erythrocytes due to an increase in their hemolysis. Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common erythrocyte enzyme defects related to hemolysis. T