Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Gebeşçe, Arzu"'
Publikováno v:
In International Journal of Pediatric Otorhinolaryngology August 2012 76(8):1145-1147
Autor:
GEBEŞÇE, Arzu1 agebesce@fatih.edu.tr, USLU, Haşim2, KELEŞ, Esengül1, YILDIRIM, Aydın2, GÜRLER, Bülent2, YAZGAN, Hamza1, BAŞTÜRK, Bülent1, DEMİRDÖVEN, Mehmet1, TONBUL, Alparslan1
Publikováno v:
Turkish Journal of Medical Sciences. 2016, Vol. 46 Issue 2, p315-320. 6p.
Autor:
Gebeşçe, Arzu1 agebesce@fatih.edu.tr, Uslu, Haşim2, Keleş, Esengül1, Demirdöven, Mehmet1, Tonbul, Alparslan1, Baştürk, Bülent1, Yazgan, Hamza1
Publikováno v:
Dicle Medical Journal / Dicle Tip Dergisi. 2015, Vol. 42 Issue 2, p137-142. 6p.
Publikováno v:
Volume: 19, Issue: 2 86-87
Gaziantep Medical Journal
Gaziantep Medical Journal
We aimed to evaluate the results of 5 years of rotavirus vaccination experience and compare the effects of monovalent and pentavalent vaccines. This retrospective study included 2345 children vaccinated in a trial that was held between January 2007 a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::6ff35b8cba6713a17802c808286622de
https://dergipark.org.tr/tr/pub/gantepmj/issue/6513/86326
https://dergipark.org.tr/tr/pub/gantepmj/issue/6513/86326
Publikováno v:
Volume: 37, Issue: 1 11-15
Zeynep Kamil Tıp Bülteni
Zeynep Kamil Tıp Bülteni
Objective: In children with measles infection we aimed to assess prospectively the serum aspartat-and alanin aminotransferase levels fort he evaluation of hepatic involvement and serum amilase levels for the pancreatic involvement. Materials and Meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::3bdc2b730a2a0df966115b12c7f716b6
https://dergipark.org.tr/tr/pub/zktipb/issue/22058/236852
https://dergipark.org.tr/tr/pub/zktipb/issue/22058/236852
Publikováno v:
Epilepsi: Journal of the Turkish Epilepsi Society. 2012, Vol. 18 Issue 3, p30-32. 3p.
Publikováno v:
Case Reports in Pediatrics.
Smith-Lemli-Opitz syndrome is an autosomal recessive disease of cholesterol metabolism. It is a multiple malformation syndrome with typical dysmorphic features such as bitemporal narrowing, ptosis, epicanthus, microcephaly, micrognathia, and cardiova
Publikováno v:
ISRN Pediatrics; 2013, p1-4, 4p
Publikováno v:
ISRN Pediatrics; 2012, p1-4, 4p
Akademický článek
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