Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Tuba Koçkar"'
Publikováno v:
Korean Journal of Pediatrics, Vol 61, Iss 7, Pp 217-220 (2018)
Purpose Type 1 diabetes mellitus (T1DM) is a chronic and immune-mediated disease, which is characterized by the progressive destruction of pancreatic beta cells. T1DM precipitates in genetically susceptible individuals through environmental factors.
Externí odkaz:
https://doaj.org/article/51d1e7af77404917bfb093da1339e540
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Volume: 21, Issue: 1 83-85
Çocuk Dergisi
Çocuk Dergisi
In this report, a ten-year-old boy was presented with a history of chronic diarrhea, recurrent wheezing, recurrent respiratory infections, finger clubbing, and growth retardation. Due to bronchiectasis in the chest tomography, low gaita elastase leve
Publikováno v:
Korean Journal of Pediatrics
Purpose Type 1 diabetes mellitus (T1DM) is a chronic and immune-mediated disease, which is characterized by the progressive destruction of pancreatic beta cells. T1DM precipitates in genetically susceptible individuals through environmental factors.
Autor:
Ayse Ayzit Atabek, Sevgi Pekcan, Şafak Göktaş, Sedat Oktem, Ozgur Kasapcopur, Haluk Çokuğraş, Ebru Senol, Saniye Girit, Tuba Koçkar Kizilirmak
Publikováno v:
Arch Rheumatol
Objectives: This study aims to analyze the coherence between T-SPOT tuberculosis test (T-SPOT.TB) and tuberculin skin test (TST) with different cut-off values in screening latent tuberculosis infection (LTBI) both prior to and at the sixth month of a
Autor:
Yuksel Barut, Sezen Ugan Atik, İlker Tolga Özgen, Servet Erdal Adal, Tuba Koçkar, Semra Gürsoy
Publikováno v:
İstanbul Kanuni Sultan Süleyman Tıp Dergisi.
Publikováno v:
Turk pediatri arsivi. 51(4)
AIM Galactosemia is a carbohydrate metabolism disorder with autosomal recessive inheritance. The most frequent enzyme deficiency is galactose-1-phosphate-uridylytransferase, which causes classic galactosemia. When the enzyme is absent, an infant cann