Ara
Toplam kayıt 69, listelenen: 41-50
Kanser Tanısı Alan Çocuk/Ergenlerin Onay Sürecine ve Tedaviye Katılımlarının Değerlendirilmesi
(2016)
Kanser gibi yaşamı tehdit eden hastalık durumunda hekimler arasında tıbbi gerçeğin hastaya söylenmesi eğilimi her ülkenin kendi ahlaksal, sosyal ve kültürel yapısına göre farklılık gösterebildiği gibi, ülkelerin sağlık ...
Association of Synapsin III Gene with Adult Attention Deficit Hyperactivity Disorder
(Mary Ann Liebert, Inc, 2013)
It was aimed to investigate the association of the synapsin III gene -196 G> A and -631 C>G polymorphisms that takes place in an encoding presynaptic protein, with adult attention deficit hyperactivity disorder (ADHD). One ...
8 Melatonin, quercetin and resveratrol attenuates oxidative hepatocellular injury in streptozotocin-induced diabetic rats
(Sage Publications Ltd, 2015)
In this study, effects of melatonin, quercetin and resveratrol on hepatocellular injury in streptozotocin (STZ)-induced experimental diabetes were aimed to be investigated by histological and biochemical methods. Thirty-five ...
Bağımlılığın Patofizyolojisi
(2019)
Alkol, sigara ve yasaklı maddelerin kullanımı, yol açtığı sağlık problemlerinin yanında, iş gücünde kayba ve suça eğilimde artmaya sebep olmasıyla, ortaya çıkan maddi ve manevi hasarı daha da arttırmaktadır. Bağımlılık ...
Anatomy and variations of plantaris muscle in fetuses
(Anatomical Soc India, 2015)
Introduction: We have aimed at researching into the morphometric development and variations of the plantaris muscle and its tendon throughout the fetal period and comparing them with the results of the study performed on ...
Simultaneous Repair of Isolated Bilateral Congenital External Auditory Canal Atresia: Case Report and Review of the Literature
(Mediterranean Soc Otology & Audiology, 2013)
Congenital external auditory canal(EAC) atresia describes the condition of an embryologically malformed external auditory canal. The widely accepted incidence of aural atresia is one in 10,000 to 20,000 live births. The ...
Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency
(Galenos Yayincilik, 2016)
Objective: Deficiency of steroid 5-alpha reductase type 2 (5 alpha RD2) is a rare autosomal recessive disorder caused by mutations in the SRD5A2 gene. A defect in the 5-alpha reductase enzyme, which ensures conversion of ...
Determination of Phthalates Migrating from Plastic Containers into Beverages
(Springer, 2015)
The determination of phthalates in beverages (soda, lemonade, cola, mineral water) sold in Turkish markets was carried out using gas chromatography-mass spectrometry (GC-MS). The mean phthalate concentrations were determined ...
Radiological Investigation on the Hand Development in Human Fetuses Throughout the Fetal Period and an Evaluation Performed in Terms of its Clinical Importance Hand Development
(Soc Chilena Anatomia, 2016)
It was aimed in this study that the morphometric development of the hand in human fetuses throughout the fetal period be radiologically investigated and the clinical importance of this period be evaluated. A total of 50 ...
Aminoguanidine mitigates apoptosis, testicular seminiferous tubules damage, and oxidative stress in streptozotocin-induced diabetic rats
(Churchill Livingstone, 2015)
This study aimed to investigate the effect of aminoguanidine (AG) against testicular damage streptozotocin (STZ) induced diabetes. Thirty two rats were separated into four groups: control, AG, STZ and STZ + AG. In the STZ ...