Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Elif Kazancı"'
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:
Hacer Ergin, Özmert M.A. Özdemir, Abdullah Karaca, Nilay Şen Türk, Füsun Düzcan, Şeniz Ergin, Elif Kazancı, Canan Vergin, Ayşe Erbay
Publikováno v:
Pediatrics and Neonatology, Vol 56, Iss 4, Pp 271-274 (2015)
Congenital leukemia is a rare disease. The majority of cases of this disease are acute myelogenous leukemia (AML). Congenital acute lymphoblastic leukemia (ALL) is rare and most often is of B cell lineage. Rarely, some cases have been designated biph
Externí odkaz:
https://doaj.org/article/473001f3801645089bab7d7149aa5ca6
Publikováno v:
Turkish Journal of Hematology, Vol 28, Iss 01, Pp 63-67 (2011)
We report two male cases (4- and 5-years-old) of intrathecal methotrexate overdose. The two boys with acute lymphoblastic leukemia were to receive intrathecal injection of methotrexate. Instead of the prescribed 12 mg, they both received a dose of 12
Externí odkaz:
https://doaj.org/article/f2c122812da74c4b9a5dd91d7cd71fd5
Autor:
Fatih Demircioğlu, Elif Kazancı, Dildar Bahar Genç, Hakan Erdoğan, Sevil Bilir Göksügür, Mervan Bekdaş
Publikováno v:
Turkish Journal of Hematology, Vol 30, Iss 4, Pp 426-428 (2013)
Externí odkaz:
https://doaj.org/article/819e80c94b53411c9f3c32f65f558762
Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 23(2)
May-Hegglin anomaly is a hereditary thrombocytopenia associated with giant platelets and large basophilic, cytoplasmic inclusion bodies (resembling Döhle bodies) in the granulocytes. Patients may experience easy bruising, recurrent epistaxis, gingiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1f4853429c5b7339d0ff355b05695e8c
https://pubmed.ncbi.nlm.nih.gov/27265293
https://pubmed.ncbi.nlm.nih.gov/27265293
Autor:
Hüseyin, Gülen, Elif, Kazancı, Demir Gökçer, Özek, Ayşe, Erbay, Selcan, Yamacı, Safiye, Aktaş, Canan, Vergin
Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 22(3)
Calcinosis cutis, an uncommon disorder characterized by hydroxyapatite crystals of calcium phosphate deposited in the skin, has been described infrequently in childhood. Cutaneous calcification may be divided into four major categories: dystrophic, m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::679651c13aa69a71c41fc3a55fdb9629
https://pubmed.ncbi.nlm.nih.gov/27264837
https://pubmed.ncbi.nlm.nih.gov/27264837
Publikováno v:
The Journal of Tepecik Education and Research Hospital. 15:85-89
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03fc4ea3280fb341189c8f266db3c21f
https://doi.org/10.5222/terh.2005.67348
https://doi.org/10.5222/terh.2005.67348