Başkent University

About: Başkent University is a education organization based out in Ankara, Turkey. It is known for research contribution in the topics: Transplantation & Population. The organization has 4652 authors who have published 10380 publications receiving 143117 citations. The organization is also known as: Başkent Üniversitesi.

Impaired coronary flow reserve in hemodialysis patients: a transthoracic Doppler echocardiographic study.

Abstract: Background: Coronary flow reserve (CFR) reflects the functional capacity of microcirculation to adapt to blood demand during increased cardiac work. In this study, CFR of hemodialys

Epidemiology of Pediatric Burn Injuries in Southern Turkey

Abstract: The aim of this study was to identify the epidemiological features of pediatric burn injuries in southern part of Turkey. In this retrospective study, 137 hospitalized pediatric patients (85 men and 52 women) who were admitted to our burn unit during a period of 3 years were analyzed. Pediatric patients were categorized into three groups: the infants and toddlers (0-2 years), early childhood (3-6 years), and late childhood (7-15 years). Epidemiological data included age, sex, location, the cause and type, and place of burn. In the first two groups, scalding (95.1% and 86.7%, respectively) was the predominant cause of burn whereas in late childhood electric burns (51.4%) were a more common occurrence. No differences were found between the groups with respect to mean TBSA and full-thickness burns. A total of 15 (10.1%) patients died during the study period. A total of 74.4% of burn injuries occurred at home, and almost all were preventable, with 16 % of the burns occurring in the autumn; however, 42% occurred in the summer. These findings will be used as a basis for developing targeted preventive programs to protect children from burns. We also consider it is necessary to educate children and their parents about the prevention of burn injuries.

Administration of B-group vitamins reduces circulating homocysteine in polycystic ovarian syndrome patients treated with metformin: a randomized trial

Abstract: BACKGROUND: The aim of the current study was to assess the effects of B-group vitamins and folic acid administration on serum levels of homocysteine (Hcy) in patients with polycystic ovarian syndrome (PCOS) on shortterm metformin treatment. METHODS: Patients were randomly assigned to one of three treatment groups. Group 1 patients (n 5 20) received metformin (850mg twice daily); group 2 patients (n 5 20) received metformin (850mg twice daily) and B-group vitamins (vitamin B1, 250mg; vitamin B6, 250mg; vitamin B12, 1000mg twice daily); and group 3 patients (n 5 20) received metformin (850mg twice daily) and folic acid (174mg twice daily). In all groups, lipid profiles and plasma total Hcy, vitamin B12, folic acid and glucose levels were recorded at baseline and at 3 months. RESULTS: A 26.5% increase in Hcy levels was seen after 12 weeks of metformin therapy, while 21.17 and 8.33% decreases in Hcy levels were detected when B-group vitamins or folic acid plus metformin were given respectively. There were no statistically significant differences recorded in insulin sensitivity using homeostasis model assessment in the three groups. CONCLUSION: These findings suggest that B-group vitamins and folic acid administration counteract the Hcy-increasing effect seen with metformin therapy.

Effect of flowable composite lining on microleakage and internal voids in Class II composite restorations.

Abstract: PURPOSE The aim of this study was to determine the influence of four flowable composite linings on marginal microleakage and internal voids in Class II composite restorations with the margins above the cementoenamel junction (CEJ). MATERIALS AND METHODS Class II cavities were randomly divided into 8 groups (n = 10). Group 1: One Step Plus/Aelite LS Packable; group 2: One Step Plus/Aelite Flow/Aelite LS Packable; group 3: Comfort Bond/Solitaire 2; group 4: Comfort Bond/Flowline/Solitaire 2; group 5: Solobond M/Grandio; group 6: Solobond M/Grandio Flow/Grandio; group 7: Admira Bond/Admira; Group 8: Admira bond/Admira Flow/Admira. After restoration, all teeth were stored for 24 h, thermocycled (at 5 degrees C to 55 degrees C) 500 times, and soaked in 0.5% basic fuchsin dye for 24 h. After soaking, the teeth were sectioned and observed under a stereomicroscope. Gingival marginal microleakage and internal voids (at the gingival wall interface and in the cervical and the occlusal parts) were recorded. Data were analyzed with the Mann-Whitney U- and Kruskal-Wallis tests (p < 0.05). RESULTS Statistical analyses indicated that the use of flowable resin composites provided a reduction in microleakage in groups 6 and 8. Groups 2 and 4 showed fewer voids in the cervical area than without flowable composites. CONCLUSION It was concluded that none of the materials tested was able to eliminate the marginal microleakage on the cervical wall. Flowable resin composites under nanohybrid (group 6) and ormocer (group 8) composites provided a significantly different reduction in microleakage compared to restorations without flowable liners. Fewer cervia voids were observed in packable composites with flowable liner (groups 2 and 4) than without flowable liner (groups 1 and 3s).

Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene.

Abstract: Background The progressive myoclonus epilepsies (PMEs) comprise a group of clinically and genetically heterogeneous disorders characterised by myoclonus, epilepsy, and neurological deterioration. This study aimed to identify the underlying gene(s) in childhood onset PME patients with unknown molecular genetic background. Methods Homozygosity mapping was applied on genome-wide single nucleotide polymorphism data of 18 Turkish patients. The potassium channel tetramerisation domain-containing 7 ( KCTD7 ) gene, previously associated with PME in a single inbred family, was screened for mutations. The spatiotemporal expression of KCTD7 was assessed in cellular cultures and mouse brain tissue. Results Overlapping homozygosity in 8/18 patients defined a 1.5 Mb segment on 7q11.21 as the major candidate locus. Screening of the positional candidate gene KCTD7 revealed homozygous missense mutations in two of the eight cases. Screening of KCTD7 in a further 132 PME patients revealed four additional mutations (two missense, one in-frame deletion, and one frameshift-causing) in five families. Eight patients presented with myoclonus and epilepsy and one with ataxia, the mean age of onset being 19 months. Within 2 years after onset, progressive loss of mental and motor skills ensued leading to severe dementia and motor handicap. KCTD7 showed cytosolic localisation and predominant neuronal expression, with widespread expression throughout the brain. None of three polypeptides carrying patient missense mutations affected the subcellular distribution of KCTD7. Discussion These data confirm the causality of KCTD7 defects in PME, and imply that KCTD7 mutation screening should be considered in PME patients with onset around 2 years of age followed by rapid mental and motor deterioration.