Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Cem Gokcen"'
Autor:
Meryem Ozlem Kutuk, Ali Evren Tufan, Fethiye Kilicaslan, Cem Gokcen, Gulen Guler Aksu, Cigdem Yektas, Hasan Kandemir, Fatma Celik, Tuba Mutluer, Ahmet Buber, Mehmet Karadag, Nurdan Coban, Seyma Coskun, Zehra Hangul, Ebru Altintas, Ufuk Acikbas, Asli Giray, Yeliz Aka, Bilkay Basturk, Ozgur Kutuk
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract The etiology of tic disorders (TDs) is not precisely known, although several lines of evidence suggest involvement of the immune system in pathogenesis. Here, we aimed to determine the expression levels of pro-inflammatory and anti-inflammat
Externí odkaz:
https://doaj.org/article/b9f73835a2c84b68a9775c2465c3b577
Autor:
Meryem Ozlem Kutuk, Ali Evren Tufan, Fethiye Kilicaslan, Pınar Vural, Cem Gokcen, Sevay Alsen Guney, Bahtim Kutuk, Gonca Ozyurt, Neslihan Inal, Tuba Mutluer, Eren Yavuz Acikalin, Fadime Hande Ozer, Esma Nur Pamuk, Seyma Celikcan Yesilmese, Mehmet Karadag, Zehra Hangul, Cilem Bilginer, Nilfer Sahin, Oznur Bilac, Hasan Kandemir, Eyup Sabri Ercan, Tugba Eseroglu Soylemez, Sadettin Burak Acikel, Gulen Guler Aksu, Pelin Dag, Fevziye Toros, Caner Mutlu, Omer Kardas, Burcu Kardas, Suleyman Kizildag, Esra Demirci, Sevgi Ozmen, Leyla Sevicin, Yuksel Sumeyra Karagoz, Umit Isik, Evrim Aktepe, Hatice Altun, Çigdem Yektas, Berna Polat Tuysuz, Ahmet Buber, Mehmet Akif Cansiz, Hakan Ogutlu, Safak Eray, Hande Ayraler Taner, Ebru Altintas, Ozgur Kutuk
Publikováno v:
Heliyon, Vol 9, Iss 10, Pp e20766- (2023)
The aim of this study is to determine the functioning of adults with autism spectrum disorders (ASDs) diagnosed in childhood and depression and burnout levels among their parents. A total of 261 adults with ASDs and their parents were recruited for t
Externí odkaz:
https://doaj.org/article/49ab186ff7fe494eb1e5cee61977ea80
Publikováno v:
Medicine Science, Vol 7, Iss 1, Pp 232-234 (2018)
Osteogenesis Imperfecta (OI) is a rare, autosomally inherited disorder of the connective tissue matrix that is characterized by bone fractures, deafness, and blue sclera. The impairment of Type 1 collagen production causes frequent fractures and incr
Externí odkaz:
https://doaj.org/article/ef25ac9bd8a14207bceb680e2a283bb7
Publikováno v:
International Journal of Medical Sciences, Vol 8, Iss 7, Pp 523-528 (2011)
Objective: The purpose of this study was to evaluate the relationship between 5,10- methylenetetrahydrofolate reductase (MTHFR) polymorphisms and Attention Deficit Hyperactivity Disorder (ADHD) in a sample of Turkish children.Study Design: MTHFR gene
Externí odkaz:
https://doaj.org/article/1b4ae71053b04e38824bb7e1ffa79dd6
Autor:
Meryem Ozlem Kutuk, Fethiye Kilicaslan, Ali Evren Tufan, Fatma Celik, Cem Gokcen, Harika Gozukara Bag, Gulay Servi, Mehtap Karali, Gamze Bahsi, Ceyhun Servi, Resat Alatli, Betul Kandemir, Neslihan Aytekin, Ozgur Kutuk
Publikováno v:
Children's Health Care. :1-17
Autor:
Onur Burak Dursun, Bahadır Turan, Yaşar Tanir, İbrahim Selçuk Esin, Cem Gokcen, Nusret Soylu, Murat Coskun, Seda Erbilgin, Hicran Dogru, İlyas Kaya, Ayşe Kutlu, Aybuke Tugce Mustan, Ali Karayagmurlu, Murat Gulsen, Ayşe Rodopman Arman
Publikováno v:
Telemedicine and e-Health
Background: This article presents the results of a comprehensive national model developed for managing maladaptive behaviors (MBs) in children with mental special needs (CMSNs) during the coronavirus disease 2019 (COVID-19) pandemic that combines tel
Autor:
Neslihan İnal, Birim Günay Kiliç, Dilek Ozgul, Cem Gokcen, Zehra Topal, Gonca Özyurt, Dogukan Koc, Mert Besenek, Canem Kavurma, Rasim Somer Diler, Ipek Percinel Yazici, Merve Cikili Uytun, Öznur Bilaç, Berna Karabina, Şafak Eray, Şermin Yalın Sapmaz, Mustafa Tuncturk, Ömer Faruk Akça, Gul Karacetin, Çağatay Ermiş, Sena Aksoy
Publikováno v:
Acta Psychiatrica Scandinavica. 145:200-208
Objective Pediatric bipolar disorder (PBD) is a serious, recurrent disorder leading to severe functional impairment. As a first mood episode, index episode could affect the long-term course of the illness. This study aimed to investigate the clinical
Publikováno v:
Clinical Psychopharmacology and Neuroscience
Objective Although attention deficit hyperactivity disorder (ADHD) is a disease with high genetic transition, our knowledge about the mechanism of the disease is limited. In this study, it was aimed to evaluate the levels of miR-132-3p and miR-942-5p
Publikováno v:
Volume: 7, Issue: 1 88-96
Middle Black Sea Journal of Health Science
Middle Black Sea Journal of Health Science
Objective: Physical and mental health are closely related. Psychiatric problems increase in the presence of a physical illness. Consultation liaison psychiatry provides a combination of medical treatment, psychiatric treatment, and psychosocial care
Publikováno v:
Dicle Medical Journal, Vol 48, Iss 1, Pp 187-196 (2021)
Objective: We aimed to determine the sociodemographic characteristics of children who are referred to the Gaziantep University Faculty of Medicine Child and Adolescent Psychiatry Clinic by the judicial authorities, to determine the causes of forensic