Zobrazeno 1 - 10
of 58
pro vyhledávání: '"YUCA, Sevil Ari"'
Autor:
Yuca, Sevil Ari, Rendtorff, Nanna Dahl, Boulahbel, Houda, Lodahl, Marianne, Tranebjærg, Lisbeth, Cesur, Yasar, Dogan, Murat, Yilmaz, Cahide, Akgun, Cihangir, Acikgoz, Mehmet
Publikováno v:
In European Journal of Medical Genetics January 2012 55(1):37-42
Autor:
Cesur, Yasar1, Yuca, Sevil Ari2, Bektas, Selcuk3, Yilmaz, Cahide3, Temel, Hayrettin3, Dulger, Haluk4
Publikováno v:
European Journal of General Medicine. 2016, Vol. 13 Issue 1, p16-20. 5p.
Autor:
Yuca, Sevil Ari1 sevilyuca@yahoo.com, Cesur, Yasar1, Yilmaz, Cahide1, Mazicioglu, Mumtaz2, Kurtoglu, Selim2
Publikováno v:
Pakistan Journal of Medical Sciences. 2011, Vol. 27 Issue 1, p115-119. 5p. 5 Charts.
Autor:
Yuca, Sevil Ari1, Ceylan, Abdullah1, Çaksen, Hüseyin1, Kirimi, Ercan1, Yilmaz, Cahide1, Bay, Ali1
Publikováno v:
Journal of Pediatric Infectious Diseases. 2006, Vol. 1 Issue 4, p225-229. 5p. 4 Charts.
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Objective: The aim of this study was to estimate the prevalence of overweight and obesity in school children in Eastern Turkey. Methods: This study included 9048 school children aged 6−18 years. The subjects were classified as overweight and obese,
Publikováno v:
Volume: 7, Issue: 4 419-425
European Journal of General Medicine
European Journal of General Medicine
Review of the literature was performed to define the optimal treatment of patients with juvenile nasopharyngeal angiofibroma (JNA). The prognosis for this disease is extremely good if diagnosed well in time and if the tumor has not extended intracran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::52ce48516c17ca23bc6a39f26b4b7b80
https://dergipark.org.tr/tr/pub/ejgm/issue/5303/71873
https://dergipark.org.tr/tr/pub/ejgm/issue/5303/71873
Akademický článek
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Autor:
Yilmaz, Cahide, Dogan, Murat, Cesur, Yaşar, Caksen, Huseyin, Yuca, Sevil Ari, Atas, Bulent, Tuncer, Oguz
Arginine succinate lyase (ASL) deficiency is one of the most common cause of urea cycle defect and shows all characteristics of this disorders. This disease is presented with hyperammonemia, abnormally kinky hair and mental retardation. 6-years-old-g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::14a9a95ab80ee75ae2a041b86b2da547
https://avesis.yyu.edu.tr/publication/details/55bb60c7-ec83-48c1-abb7-8402165930b3/oai
https://avesis.yyu.edu.tr/publication/details/55bb60c7-ec83-48c1-abb7-8402165930b3/oai