Chronic cough in children is among the problems that lead to frequent consultations with a
doctor. In this study, we attempted to research the reasons for chronic cough by an evaluation …

Molybdenum cofactor deficiency is a rare inborn error of metabolism. The major clinical
symptoms are intractable neonatal seizures, progressive encephalopathy, facial dysmorphic …

Objectives This study aims to investigate whether there was a difference between
epinephrine (EPN) and tranexamic acid (TXA) in providing visual clarity during arthroscopic …

Objective Rapid-onset obesity with hypoventilation, hypothalamic dysfunction, and autonomic
dysregulation (ROHHAD) is a rare disorder that mimics both common obesity and genetic …

Congenital myasthenic syndromes are clinically and genetically heterogeneous disorders
of neuromuscular transmission. Most are treatable, but certain subtypes worsen with …

Guillain-Barré syndrome (GBS) and transverse myelitis may occur coexistently in the pediatric
population. This may be explained by a shared epitope between peripheral and central …

The aim of this study is to analyze the epidemiology of the clinical and genetic features of
childhood-onset limb-girdle muscular dystrophies (LGMD) in the Aegean part of Turkey. In total …

Introduction In this retrospective study, the impact of age, amputation level and the cause of
amputation were examined using the Hospital Anxiety and Depression Scale (HADS) and …

Aim We aimed to describe the prevalence and significance of white matter lesions detected
on magnetic resonance imaging ( MRI ) in children with headache. Material and Methods …

Population-based studies suggest that seizure incidence is highest during the first year of
life, and early-life seizures frequently result in the development of epilepsy and behavioral …