Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Meral Türker"'
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:
Burcak Tatlı Güneş, Zühal Önder Siviş, Eda Ataseven, Barış Malbora, Meral Türker, Burcu Fatma Belen, Berna Atabay, Tahir Atik, Esra Işık, Ferda Özkınay
Publikováno v:
Turkish Journal of Hematology, Vol 35, Iss 3, Pp 202-203 (2018)
Externí odkaz:
https://doaj.org/article/8d7642aae4a240ef9466a15fa5d2a943
Publikováno v:
Turkish Journal of Hematology, Vol 30, Iss 1, Pp 58-62 (2013)
Central nervous system (CNS) involvement of Epstein-Barr virus (EBV)-associated lymphoproliferative disease is a rare and serious complication in children with leukemia. Although rituximab therapy seems to be promising in these cases, persistent hypo
Externí odkaz:
https://doaj.org/article/eaa26bb31f344a8b9c967762e0eb5b02
Autor:
Tunç Fışgın, Can Balkan, Tiraje Celkan, Yurdanur Kılınç, Meral Türker, Çetin Timur, Türkiz Gürsel, Emin Kürekçi, Feride Duru, Alphan Küpesiz, Lale Olcay, Şebnem Yılmaz, Ünsal Özgen, Ayşegül Ünüvar
Publikováno v:
Turkish Journal of Hematology, Vol 29, Iss 1, Pp 48-54 (2012)
OBJECTIVE: We evaluated the clinical findings, laboratory data, management, and outcome of children with rare coagulation deficiencies (RCDs) diagnosed in Turkey during the past 10 years, retrospectively. METHODS: A simple Excel file of questionnaire
Externí odkaz:
https://doaj.org/article/b65dd265f1644bb7aafcb81e15161244
Autor:
Burcu Belen, Özlem Çakıcı, Melikşah Uzakgider, Haldun Öniz, Meral Türker, Berna Atabay, Barış Malbora, Levent Karapınar
Publikováno v:
Turkish Journal of Hematology, Vol 34, Iss 2, Pp 179-180 (2017)
Externí odkaz:
https://doaj.org/article/074c9000093e40c29d2bab904039a4f9
Publikováno v:
Turkish Journal of Hematology, Vol 27, Iss 3, Pp 147-155 (2010)
OBJECTIVE: Immune thrombocytopenic purpura (ITP) is the most common cause of acquired thrombocytopenia in children. The objective of this study was to evaluate the presenting features, variation in the clinical courses, initial response rate to thera
Externí odkaz:
https://doaj.org/article/f5007f5000cd495bbf565c5be92085fe
Autor:
Deniz Kızmazoğlu, Zuhal Önder Siviş, Burcak Tatlı Güneş, Esin Özcan, Meral Türker, Berna Atabay, Haldun Öniz
Publikováno v:
Dokuz Eylül Üniversitesi Tıp Fakültesi Dergisi. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9a0e861ff8d2cd1e02e62c1efee4396
https://doi.org/10.5505/deutfd.2021.22590
https://doi.org/10.5505/deutfd.2021.22590
Autor:
Talia Ileri, Yesim Aydinok, Ezgi Paslı Uysalol, Aydan Akdeniz, Mustafa Buyukavci, Naci Tiftik, Mehmet Akin, Berna Atabay, Akif Yesilipek, Yeşim Oymak, Turkan Patiroglu, Güçhan Alanoğlu, Arzu Akcay, Özcan Bör, Canan Vergin, Gonul Aydogan, Hüseyin Tokgöz, Sule Unal, Zeynep Karakas, Adalet Meral Güneş, Nur Soyer, Meral Türker, Elif Güler Kazanci, Mediha Akcan, Banu Oflaz, Nihal Karadaş, Selda Kahraman, Yurdanur Kilinç, Murat Söker, Süheyla Ocak, Melike Sezgin Evim, Didem Atay, Selma Unal, Umran Caliskan, Ali Bay, E. Unal
Publikováno v:
Turkish Journal of Hematology
Turkish Journal of Hematology, Vol 35, Iss 1, Pp 12-18 (2018)
Turkish Journal of Hematology, Vol 35, Iss 1, Pp 12-18 (2018)
WOS: 000426572200002
PubMed ID: 28404539
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
PubMed ID: 28404539
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e538e523242d331328a04d77b53ef89b
https://doi.org/10.4274/tjh.2017.0039
https://doi.org/10.4274/tjh.2017.0039
Autor:
Hale Ören, Özlem Tüfekçi, Meral Türker, Salih Gözmen, Gülersu Irken, Berna Atabay, Şebnem Yılmaz Bengoa, Tuba Hilkay Karapınar
Publikováno v:
Journal of Pediatric Hematology/Oncology. 39:440-444
The increased awareness about the severity of complications in thalassemia intermedia patients led authorities to develop strategies for better management and follow-up of these patients. In this study, we aimed to define the clinical and laboratory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ee20352f458a6731bbe1641149d7412
https://doi.org/10.1097/mph.0000000000000914
https://doi.org/10.1097/mph.0000000000000914
Publikováno v:
The Journal of Pediatric Research. 2:92-95
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46dc552149b19a51bbe94e99ff93f71c
https://doi.org/10.4274/jpr.30602
https://doi.org/10.4274/jpr.30602