WoS Q Kategorisi "Q2" Bildiri Koleksiyonu İçin Listeleme
Toplam kayıt 16, listelenen: 1-16
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Comparison of pediatric antibiotherapy in primary care: Low vs. high prescribers
(Wiley, 2021)... -
Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism
(Nature Publishing Group, 2018)... -
En bloc resection of bladder tumours: Histopathologic features of a prospective study
(Springer, 2021)Background and Aims: The aim of the present study was to evaluate the characteristics of patients with acute liver failure (ALF) who underwent liver transplantation (LT) at 14 centers in Turkey and to determine factors ... -
Exome sequencing in a large family with Tourette Syndrome/Chronic Tic Disorder
(Nature Publishing Group, 2018)... -
The investigation of genetic etiology in familial cases with congenital hypothyroidism
(Karger, 2019)Background: Congenital hypothyroidism(CH) is the most common neonatal endocrinological disorder in the world. Although most of the CH is sporadic, some genetic defects are responsible from the etiology. The aim of this ... -
Investigation of vitamin utilization in primary care in Istanbul
(Oxford University Press, 2020)... -
A novel candidate frameshift mutation for catecholaminergic polymorphic ventricular tchycardia
(Nature Publishing Group, 2019)...