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pro vyhledávání: '"Burcu Köksal"'
Autor:
Burcu Köksal
Publikováno v:
Archives of Medical Science, Vol 20, Iss 2, Pp 698-703 (2024)
Introduction The purpose of this study is to investigate the relationship between attentional impulsivity levels and physiological and psychological stress responses of university students. Material and methods In the study, a correlational research
Externí odkaz:
https://doaj.org/article/53f81332bf684dee82bfa94975c44ef9
Autor:
Burcu Köksal
Publikováno v:
Turkish Journal of Agriculture: Food Science and Technology, Vol 10, Iss 3, Pp 447-451 (2022)
The main purpose of this study is to compare the perceived stress level of university students in terms of body-mass index categories and gender. 235 university students (183 female, 53 male) between the ages of 18-40 participated in the study. Parti
Externí odkaz:
https://doaj.org/article/a880eaa4f35b4b4b9d87a2cf3dd83b61
Autor:
Burcu Köksal
Publikováno v:
Acta Facultatis Medicae Naissensis. 38:351-359
The purpose of this study was to examine the practical importance of the correlation values between plasma and salivary cortisol levels using meta-analysis study. In this way, researchers focusing on cortisol levels in different individuals can use m
Publikováno v:
Acta Facultatis Medicae Naissensis. 37:34-47
Publikováno v:
Medicni perspektivi (Medical perspectives); Том 24, № 4 (2019); 51-58
Медичні перспективи; Том 24, № 4 (2019); 51-58
Medičnì Perspektivi, Vol 24, Iss 4, Pp 51-58 (2019)
Медичні перспективи; Том 24, № 4 (2019); 51-58
Medičnì Perspektivi, Vol 24, Iss 4, Pp 51-58 (2019)
Diabetes mellitus is a complicated and serious health problem involving peripheral neuropathy. This situation causes to loss of senses, tingle and pain. Diabetic peripheral neuropathy (DPN) affects 236 million people around the World. Hence there is
Autor:
Burcu Köksal
Publikováno v:
Düzce Üniversitesi Bilim ve Teknoloji Dergisi.
Autor:
Burcu Köksal
Publikováno v:
Volume: 13, Issue: 4 234-239
Türkiye Çocuk Hastalıkları Dergisi
Türkiye Çocuk Hastalıkları Dergisi
Amaç: Tekrarlayan bronşiolit/hışıltı okul öncesi dönemde sık görülmektedir. Epizodik hışıltı ve çoklu tetikleyici hışıltıfenotipleri tanımlanmıştır. Çalışmamızın amacı, epizodik hışıltı (EH) ve çoklu tetikleyici h
Autor:
Halil Duzova, Ibrahim Sahin, Güner Çiçek, Basak Kayhan, Esin Güllü, Abdullah Güllü, Burcu Köksal
Publikováno v:
The Journal of Sports Medicine and Physical Fitness. 58
Background:The objectives of this study were to verify effects of step-aerobic exercise (SAE) and jogging-walking exercise (JWE) program on myokines and adipokines levels in overweight sedentary females. Methods:Volunteer subjects (N.=25) were assign
Autor:
Burcu Köksal
Publikováno v:
Open Access Macedonian Journal of Medical Sciences, Vol 3, Iss 3, Pp 380-383 (2015)
Open Access Macedonian Journal of Medical Sciences; Vol. 3 No. 3 (2015): Sep 15 (OAMJMS); 380-383
Open Access Macedonian Journal of Medical Sciences; Vol 3, No 3 (2015): Sep 15 (OAMJMS); 380-383
Open Access Macedonian Journal of Medical Sciences
Open Access Macedonian Journal of Medical Sciences; Vol. 3 No. 3 (2015): Sep 15 (OAMJMS); 380-383
Open Access Macedonian Journal of Medical Sciences; Vol 3, No 3 (2015): Sep 15 (OAMJMS); 380-383
Open Access Macedonian Journal of Medical Sciences
BACKGROUND: In the studies focusing on diabetic organisms, Streprozotocine (STZ) is a frequently used agent to induce diabetes in rats and mice. However the current studies do not represent practical importance of their statistical findings. For show
Autor:
Yasuhito Nakagawa, Chieko Aoyama, Yukiko K. Hayashi, Satomi Mitsuhashi, Ryo Taguchi, Beril Talim, Gregory A. Cox, Hiroyuki Sugimoto, Burcu Köksal, Haluk Topaloglu, Ichizo Nishino, Ros Quinlivan, Roger B. Sher, Satoru Noguchi, Ikuya Nonaka, Mana Kurihara, Kanako Goto, Minako Karahashi, Gülsev Kale, Hiroaki Mitsuhashi, Tomoko Koumura, Aya Ohkuma, Caroline Sewry, Kazutaka Ikeda
Publikováno v:
The American Journal of Human Genetics. 88(6):845-851
Congenital muscular dystrophy is a heterogeneous group of inherited muscle diseases characterized clinically by muscle weakness and hypotonia in early infancy. A number of genes harboring causative mutations have been identified, but several cases of