Objective: The study aims to examine family functionality, emotion regulation difficulties, preference for loneliness, social exclusion, internalizing and externalizing disorders, and executive functions in children with Attention Deficit Hyperactivity Disorder (ADHD) and Cognitive Disengagement Syndrome (CDS) and compare with ADHD, and ADHD+ Oppositional Defiant Disorder (ODD).
Method: This study included 842 children aged 8-12 years. The subjects were categorized according to DSM-V as ADHD ( = 246), ADHD + ODD ( = 212), ADHD + CDS ( = 176), and Control group ( = 207).
This study aims to investigate the predictive and mediating relationships between emotion dysregulation, internalizing disorders, family functionality, loneliness preference, and executive functions (EF) in children with attention deficit hyperactivity disorder and cognitive disengagement syndrome (ADHD + CDS). This study included 176 children and adolescents (92 boys, 84 girls) who were diagnosed with ADHD + CDS according to the Diagnostic and Statistical Manual of Mental Disorders, the Fifth Edition criteria by a fellowship-trained child and adolescent psychiatrist, between ages 8 -12 (M = 10, SD = 1.52) with a convenience sampling method.
View Article and Find Full Text PDFThis study aimed to examine emotion dysregulation and internalizing disorders mediating the relationship between selective and sustained attention and loneliness preference in children diagnosed with attention deficit hyperactivity disorder (ADHD) and Cognitive Disengagement Syndrome (CDS). This study included 176 children and adolescents between ages 8 and 12. The solitude scale for children, Difficulties in Emotion Regulation Scale, Child Behavior Checklist, Barkley Sluggish Cognitive Tempo Scale, and CNS Vital Signs test were used.
View Article and Find Full Text PDFNeurol Neurochir Pol
March 2018
Charcot-Marie-Tooth (CMT) disease is a hereditary neurologic disease which affects the sensorial and motor fibers of the peripheral nerves. CMTX1 is an X-linked dominantly inherited subtype of CMT and is caused by mutations in gap junction beta 1 gene (GJB1). A small proportion of GJB1 mutations are associated with recurrent central nervous system findings.
View Article and Find Full Text PDFBackground: Donations in Turkey are insufficient to cover the high transfusion needs arising from large numbers of thalassemia and sickle cell anemia patients and increasing demands for blood due to advanced surgery and cancer treatment. The most acceptable means to get blood is voluntary blood donation and the blood donor system in Turkey mostly depends on a combination of voluntary and involuntary donors. The main aim of this study is to explore the motivations of Turkish voluntary blood donors toward blood donation and to determine predictors of blood donation motivation.
View Article and Find Full Text PDFA hitherto unreported duplication of the parotid duct in a 63-year-old man is reported. The ducts were found in the right cheek during cadaver dissection. The surrounding connective tissue of the ducts was removed and a photograph was taken.
View Article and Find Full Text PDFAnatomical variations of the first extensor compartment of the wrist are important during surgical operations of the wrist with de Quervain's disease. We studied 41 wrists from cadavers (16 whole cadavers and nine forearms) and the wrists of twenty-eight patients with de Quervain's disease to determine the variations of tendons and septa in the first extensor compartment. In 85.
View Article and Find Full Text PDFThis investigation was designed to extend our present knowledge of the origin of the anterior spinal a. and is based on 80 brains of human cadavers. The anterior spinal a.
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