Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Gönül Aydoğan"'
Publikováno v:
Bezmiâlem Science, Vol 10, Iss 6, Pp 691-697 (2022)
Objective:Acute lymphoblastic leukemia (ALL) is the most prevalent type of cancer in children. Minimal residual disease (MRD) is still the most important indicator of clinical results and relapse after chemotherapy. Multidrug resistance is the main o
Externí odkaz:
https://doaj.org/article/59cb805163264ea4a1b823eb4256d861
Autor:
Yeşim Aydınok, Yeşim Oymak, Berna Atabay, Gönül Aydoğan, Akif Yeşilipek, Selma Ünal, Yurdanur Kılınç, Banu Oflaz, Mehmet Akın, Canan Vergin, Melike Sezgin Evrim, Ümran Çalışkan, Şule Ünal, Ali Bay, Elif Kazancı, Talia İleri, Didem Atay, Türkan Patıroğlu, Selda Kahraman, Murat Söker, Mediha Akcan, Aydan Akdeniz, Mustafa Büyükavcı, Güçhan Alanoğlu, Özcan Bör, Nur Soyer, Nihal Özdemir Karadaş, Ezgi Uysalol, Meral Türker, Arzu Akçay, Süheyla Ocak, Adalet Meral Güneş, Hüseyin Tokgöz, Elif Ünal, Naci Tiftik, Zeynep Karakaş
Publikováno v:
Turkish Journal of Hematology, Vol 35, Iss 1, Pp 12-18 (2018)
Objective: The Turkish Society of Pediatric Hematology set up a National Hemoglobinopathy Registry to demonstrate the demographic and disease characteristics of patients and assess the efficacy of a hemoglobinopathy control program (HCP) over 10 year
Externí odkaz:
https://doaj.org/article/ddb5427c3e23457d87b7b6e9ef919f94
Autor:
Müge Sayitoğlu, Yücel Erbilgin, Özden Hatırnaz, İnci Yıldız, Tiraje Celkan, Sema Anak, Ömer Devecioğlu, Gönül Aydoğan, Serap Karaman, Nazan Sarper, Çetin Timur, Ümit Üre, Uğur Özbek
Publikováno v:
Turkish Journal of Hematology, Vol 29, Iss 4, Pp 325-333 (2012)
OBJECTIVE: T-cell acute lymphoblastic leukemia (T-ALL) is associated with recurrent chromosomal aberrations and abnormal ectopic gene expression during T-cell development. In order to gain insight into the pathogenesis of T-ALL this study aimed to me
Externí odkaz:
https://doaj.org/article/b81ce4f098fd45aea7c8caae301e35cf
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
Autor:
Gonca Keskindemirci, Deniz Tuğcu, Gönül Aydoğan, Arzu Akçay, Nuray Aktay Ayaz, Ali Er, Ensar Yekeler, Bilge Bilgiç
Publikováno v:
Case Reports in Pediatrics, Vol 2015 (2015)
Kasabach-Merritt phenomenon (KMP) is characterized by vascular tumour and consumptive coagulopathy with life-threatening thrombocytopenia, prolonged prothrombin time and partial thromboplastin time, hypofibrinogenemia, and the presence of high fibrin
Externí odkaz:
https://doaj.org/article/f130fc78410f469ea606d1561d6775f4
Autor:
Gonca Keskindemirci, Nuray Aktay Ayaz, Esin Aldemir, Çiğdem Aydoğmuş, Gönül Aydoğan, Sultan Kavuncuoğlu
Publikováno v:
Case Reports in Pediatrics, Vol 2014 (2014)
Familial Mediterranean Fever is an autosomal recessive disease. Major symptoms of disease are recurrent fever accompanied by serositis attacks. The disease is usually diagnosed before 20 years of age. Symptoms related to FMF are noted when children b
Externí odkaz:
https://doaj.org/article/14325301cce14301a179466fc2074413
Autor:
Sibel Akpınar Tekgündüz, Gönül Aydoğan, Cengiz Bayram, Gül Nihal Özdemir, Ezgi Paslı Uysalol, Şadan Hacısalihoğlu, Esra Arslantaş, Ali Ayçiçek
Publikováno v:
LLM Dergi. 5:70-72
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac5e96deffac63fec1c941d7007a00f4
https://doi.org/10.5578/llm.20219604
https://doi.org/10.5578/llm.20219604
Autor:
Ferhan Akici, Zafer Salcioglu, Ezgi Paslı Uysalol, Gül Nihal Özdemir, Cengiz Bayram, Elif Böncüoğlu, Gönül Aydoğan, Işık Odaman Al, Tuba Nur Tahtakesen Güçer, Gizem Ersoy, Müge Gökçe, Ali Aycicek
Publikováno v:
İstanbul Kanuni Sultan Süleyman Tıp Dergisi. 13:92-97
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eaa9ec8b1e4ceb9789a913f1a0160b36
https://doi.org/10.4274/iksstd.2021.49389
https://doi.org/10.4274/iksstd.2021.49389
Autor:
Gül Nihal Özdemir, Tuba Nur Tahtakesen, Ali Aycicek, Mehmet Akif Kilic, Ezgi Paslı Uysalol, Cengiz Bayram, Gönül Aydoğan
Publikováno v:
Turk Arch Pediatr
Objective This study aims to evaluate the demographic information, clinical and laboratory findings of patients with glucose 6 phosphate dehydrogenase deficiency. Material and methods We collected data by reviewing files and electronic records of 65
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19cd1a94e1b2c17d1dbf6e4d9b93b59b
https://doi.org/10.5152/turkarchpediatr.2021.20042
https://doi.org/10.5152/turkarchpediatr.2021.20042
Autor:
Mehmet Kılıç, Nihal Özdemir, Tuba Tahtakesen Güçer, Ezgi Uysalol, Cengiz Bayram, Ali Aycicek, Gönül Aydoğan
Objective: Hereditary spherocytosis is the most common erythrocyte membrane disorder characterized by splenomegaly, jaundice and anemia. The aim of this study was to evaluate the demographics, clinical and laboratory findings and treatment responses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e84ab75935d51498abd7933e8c7a5199
https://doi.org/10.22541/au.164864120.00451528/v1
https://doi.org/10.22541/au.164864120.00451528/v1
