Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Mediha Akcan"'
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
Publikováno v:
Turkish Journal of Hematology, Vol 29, Iss 2, Pp 143-149 (2012)
OBJECTIVE: The aim of this study was to document hematopoietic stem cell transplantation (HSCT) activity and trends at our treatment center. METHODS: Data collected over a 10-year period were retrospectively analyzed, concentrating primarily on types
Externí odkaz:
https://doaj.org/article/3b8810074bde4ad3ad66e0f5a9303017
Autor:
Gülcihan Ozek, Serap Aksoylar, Sema Kalkan Uçar, Ebru Canda, Mediha Akcan, Ozgür Cartı, Zuhal Onder Siviş, Yeşim Oymak, Havva Yazıcı, Bridget Bax, Fatma Derya Bulut, Merve Yoldaş Çelik, Fehime Erdem, Mahmut Çoker, Savaş Kansoy
Publikováno v:
Pediatric Blood & Cancer. 70
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4d72521d8747e331fe571fb4f764105
https://doi.org/10.1002/pbc.30334
https://doi.org/10.1002/pbc.30334
Publikováno v:
Trends in Pediatrics.
INTRODUCTION: Beta thalassemia carriers (BTC) in Turkey is observed with a frequency of 2.1%, and it is the most common cause of anemia after iron deficiency. There are few studies showing the effect of genotype on phenotype in beta thalassemia carry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19c2e23d236dad3226fa7cd967eeb7e6
https://doi.org/10.5222/tp.2021.41713
https://doi.org/10.5222/tp.2021.41713
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
Publikováno v:
Çocuk Enfeksiyon Dergisi/Journal of Pediatric Infection. 10:28-32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8381e3166864c86bf3576ce1eded0d07
https://doi.org/10.5152/ced.2015.1731
https://doi.org/10.5152/ced.2015.1731
Interleukin-1 plays an important role in the pathogenesis of systemic-onset juvenile idiopathic arthritis (SoJIA), and the use of anti-interleukin-1 therapy has been increasing. We report a case of a 14-year-old male patient with SoJIA. He was in rem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57e84e87144d2493e2b5e424b749bd46
https://europepmc.org/articles/PMC5389500/
https://europepmc.org/articles/PMC5389500/
Publikováno v:
Iranian Journal of Pediatrics
Delaying conception has increased the demand on assisted reproduction. Currently, more than 1% of children are conceived through assisted reproductive technologies (ART) worldwide and this number is likely to continue increasing (1). Like any other m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::519d31df2cd866c9475ccdf751bac5ab
http://europepmc.org/articles/PMC5045533
http://europepmc.org/articles/PMC5045533
Publikováno v:
Pediatric Transplantation. 16:779-782
Alpha-mannosidosis is a rare lysosomal storage disorder with an autosomal recessive inheritance. Deficient alpha-mannosidase activity leads to lysosomal accumulation of mannose-rich oligosaccharides. The disease characterized by mental retardation, s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1972f0a9af87000d5ad45cc46be383f
https://doi.org/10.1111/j.1399-3046.2012.01763.x
https://doi.org/10.1111/j.1399-3046.2012.01763.x