Zobrazeno 1 - 8 of 8 pro vyhledávání: '"Ender COŞKUNPINAR"'
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Akademický článek
Analysis of Chromosomal Aberrations and FLT3 gene Mutations in Childhood Acute Myelogenous Leukemia Patients
Autor: Ender Coşkunpınar, Sema Anak, Leyla Ağaoğlu, Ayşegül Ünüvar, Ömer Devecioğlu, Gönül Aydoğan, Çetin Timur, Ahmet Faik Öner, Yıldız Yıldırmak, Tiraje Celkan, İnci Yıldız, Nazan Sarper, Uğur Özbek
Publikováno v: Turkish Journal of Hematology, Vol 29, Iss 3, Pp 225-232 (2012)
OBJECTIVE: To identify the well-known common translocations and FLT3 mutations in childhood acute myelogenous leukemia (AML) patients in Turkey. METHODS: The study included 50 newly diagnosed patients in which t(15;17), t(8;21), and inv(16) chromosom
Externí odkaz: https://doaj.org/article/f78084826cb8469e8e42f70e9db5c5c6
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3
Akademický článek
The Importance of Fecal Transplantation in Personalized Medicine
Autor: Ender COŞKUNPINAR, Fagan İSLAMZADE, Elif Pelin YILMAZ, Ceyda HAYRETDAĞ ORS, Hüseyin ADAK, Ahmet YEŞILTEPE, Seyithan TÜRKSOYLU, Ahmet Cem DURAL
Publikováno v: Bezmiâlem Science, Vol 6, Iss 4, Pp 305-311 (2018)
It is known that intestinal microbiota feeding habits in healthy humans have a direct effect on the formation of intestinal microbiota, while simultaneously playing the most important role in the development of the immune system. Our aim in this stud
Externí odkaz: https://doaj.org/article/3e44a646bd374a5baf08585627feb172
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4
Akademický článek
Could the ENPP1 p.D85H Mutation be Associated with Hypophosphatemic Rickets?
Autor: Ender COŞKUNPINAR, Sakin TEKİN, Şükrü PALANDUZ, Hakan AVCI, Kıvanç CEFLE, N. Ozan TİRYAKİOĞLU, Ayşe KUBAT ÜZÜM, Refik TANAKOL, İlhan SATMAN
Publikováno v: Bezmiâlem Science, Vol 6, Iss 2, Pp 126-129 (2018)
Objective:A 35-year-old Turkish male patient was referred to us with a year-long history of joint paint and congenital hearing loss. Family history revealed more family members with hearing loss without paraneoplastic syndrome. These findings led us
Externí odkaz: https://doaj.org/article/7b1b6d715a4c4044bf609ae4faaa41ef
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6
The Impact of Personalized Medicine in the Treatment of Ventricular Septal Defects to Evaluate the Accuracy of Surgery Using 3D Printed Hearts
Autor: Ceyda Hayretdağ Örs, Zabihullah Erkin, Ender Coşkunpinar, Hakan Ceyran, Ali Can Hatemi, Mehmet Umut Evci
Publikováno v: Koşuyolu Heart Journal, Vol 21, Iss 2, Pp 174-176 (2018)
Volume: 21, Issue: 2 174-176
Koşuyolu Heart Journal
Ventricularseptal defect (VSD) is a well-known anomaly among congenital heart diseasestypically diagnosed in infancy. Defects in the ventricular septum cause aninterventricular shunt. The excess amount of mixed blood passes through thepulmonary circu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6629e685089563552302e6e03b8dbdf8
http://www.kosuyoluheartjournal.com/managete/fu_folder/2018-2/2018-21-2-174-176.pdf
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8
Akademický článek
Molecular Diagnosis Experience in Familial Mediterranean Fever: The Most Frequent Mutations in the MEFV Gene
Autor: Ender Coşkunpınar, Ayla Özvarnalı, Kıvanç Çefle, Ayşe Palanduz, Ahmet Gül, Derya Öztürk, Şükrü Öztürk, Şükrü Palanduz
Publikováno v: Haseki Tıp Bülteni, Vol 56, Iss 1, Pp 42-49 (2018)
Aim: Familial Mediterranean Fever (FMF) is the most frequent and historically the oldest autosomal recessive autoinflammatory disorder. No pathogen or auto-antibody has been shown to be associated with FMF. The disorder manifests with bouts of fever
Externí odkaz: https://doaj.org/article/90007ff78b67429ca45b4e32e8c17447
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