Zobrazeno 1 - 2
of 2
pro vyhledávání: '"SEREN, Pulat Lale"'
Autor:
BOZAYKUT, Abdulkadir, SEZER, Rabia Gönül, İPEK, ÖZAHİ İlke, PAKETÇİ, Cem, ÖZDE, Şükriye, SEREN, PULAT Lale
Publikováno v:
Volume: 41, Issue: 3 157-159
Zeynep Kamil Tıp Bülteni
Zeynep Kamil Tıp Bülteni
Laurence-Moon-Biedl syndrome is a rare, genetically autosomal recessive disorder, characterized by progressive retinal dystrophy, Polydactyly, obesity, hypogonadism, mental retardation, and renal dysfunction. A-3-months old boy with atypical face, de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::37321034c843fa4b48acd90476fc5c13
https://dergipark.org.tr/tr/pub/zktipb/issue/22076/237014
https://dergipark.org.tr/tr/pub/zktipb/issue/22076/237014
Autor:
SEZER, Gönül Rabia, YILDIRIM, Ali, BOZAYKUT, Abdulkadir, PAKETÇİ, Cem, İPEK, Özahi İlke, SEREN, Pulat Lale
Publikováno v:
Volume: 42, Issue: 2 59-65
Zeynep Kamil Tıp Bülteni
Zeynep Kamil Tıp Bülteni
Introduction and Aim: Fever is one ofthe most common complaints ofinfectious diseases. In this study, we aimed to determine mothers' knowledge of fever and by detecting the deficiencies, we aim to contribute to educational programs. Material and Meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::cc3a39448c12cbed5eb7488364ba354b
https://dergipark.org.tr/tr/pub/zktipb/issue/22079/237028
https://dergipark.org.tr/tr/pub/zktipb/issue/22079/237028