Zobrazeno 1 - 10
of 68
pro vyhledávání: '"TÜRKİZ GÜRSEL"'
Publikováno v:
Van Tıp Dergisi, Vol 27, Iss 1, Pp 17-21 (2020)
INTRODUCTION: Attention deficit hyperactivity disorder (ADHD) is one of the most common childhood psychiatric disorders and is believed to be caused by genetic and environmental factors. Various studies have reported that body iron levels and ADHD ar
Externí odkaz:
https://doaj.org/article/a1aeb09af70f433db0b0ec87f9ba8495
Autor:
Burcu Yazıcıoğlu, Zühre Kaya, Sezen Güntekin Ergün, Ferda Perçin, Ülker Koçak, İdil Yenicesu, Türkiz Gürsel
Publikováno v:
Turkish Journal of Hematology, Vol 34, Iss 2, Pp 143-150 (2017)
Objective: High-dose methotrexate (HD-MTX) is widely used in the consolidation phase of childhood acute lymphoblastic leukemia (ALL), but the roles that polymorphisms in folate-related genes (FRGs) play in HD-MTX toxicity and prognosis in children wi
Externí odkaz:
https://doaj.org/article/1cfd80f6663942e996c0af4fb15e4b7e
Publikováno v:
Turkish Journal of Hematology, Vol 32, Iss 4, Pp 317-322 (2015)
INTRODUCTION: Transcobalamin II deficiency is one of the rare causes of inherited vitamin B12 disorders in which the patients have characteristically normal or high vitamin B12 levels related to the transport defect of vitamin B12 into the cell, endi
Externí odkaz:
https://doaj.org/article/acf8edcd3d2c45dd8ca63f7fd186db9f
Publikováno v:
Turkish Journal of Hematology, Vol 31, Iss 1, Pp 49-55 (2014)
OBJECTIVE: Infections remain the major cause of unnecessary antibiotic use in pediatric outpatient settings. Complete blood count (CBC) is the essential test in the diagnosis of infections. C-reactive protein (CRP) is also useful for assessment of yo
Externí odkaz:
https://doaj.org/article/e166d40c1caa4783ae2573fb7359234b
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
Bilateral knee and right ankle osteonecrosis in an adolescent girl with acute lymphoblastic leukemia
Publikováno v:
Turkish Journal of Hematology, Vol 26, Iss 01, Pp 34-37 (2009)
Although rare, avascular necrosis of bone is a serious and incapacitating complication seen in children with acute lymphoblastic leukemia receiving high dose steroids. Here we present a 16 year-old girl who developed bilateral knee and right ankle av
Externí odkaz:
https://doaj.org/article/45d938a97ac44a179bf074ee0b083cbf
Publikováno v:
Turkish Journal of Hematology, Vol 26, Iss 03, Pp 151-153 (2009)
Granulocytic sarcoma is an extramedullary tumor composed of leukemic blasts. Isolated granulocytic sarcoma has rarely been reported in children with leukemia undergoing allogeneic stem cell transplantation. We report a case of isolated granulocytic s
Externí odkaz:
https://doaj.org/article/304ca568ddc941eb9551d681d4494d62
Publikováno v:
Van Medical Journal. 27:17-21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::942d8b8bf9a71aae77ed6231196779e9
https://doi.org/10.5505/vtd.2020.93276
https://doi.org/10.5505/vtd.2020.93276
Autor:
Türkiz Gürsel, Yazıcıoğlu B, Perçin F, Zühre Kaya, Ülker Koçak, Güntekin Ergun S, Idil Yenicesu
Publikováno v:
Turkish Journal of Hematology, Vol 34, Iss 2, Pp 143-150 (2017)
Turkish Journal of Hematology
Turkish Journal of Hematology
High-dose methotrexate (HD-MTX) is widely used in the consolidation phase of childhood acute lymphoblastic leukemia (ALL), but the roles that polymorphisms in folate-related genes (FRGs) play in HD-MTX toxicity and prognosis in children with ALL are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e61e2397f5b7b8fd3a60686183b02e65
http://www.tjh.com.tr/jvi.aspx?pdir=tjh&plng=eng&un=TJH-92603&look4=
http://www.tjh.com.tr/jvi.aspx?pdir=tjh&plng=eng&un=TJH-92603&look4=
Autor:
Ülker Koçak, Zühre Kaya, Türkiz Gürsel, Melek Isik, Idil Yenicesu, Ebru Yılmaz Keskin, Nergiz Öner, Burcu Belen Apak, Meryem Albayrak
Publikováno v:
Transfusion and Apheresis Science. 59:102728
Albayrak, Meryem/0000-0003-2711-5150 WOS:000538124200008 PubMed: 31980335 Objective: This study aims to investigate the distribution, clinical characteristics and outcome of inherited coagulation disorders (ICD) in Turkish children. Subjects and meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a2249752696b602137d6d851e46ad55
https://doi.org/10.1016/j.transci.2020.102728
https://doi.org/10.1016/j.transci.2020.102728