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The Changes of Smart Device Usage Status in Early Childhood: Comparison of 2015–2016 and 2017 Studies

So H, Lim S, Cho SY, Koh MS, Moon JH

PURPOSE: This study aimed to identify changes in smart device usage trends of young children using two studies conducted in 2015-2016 and 2017 respectively. METHODS: We compared the data of the...
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A Case of Klinefelter Syndrome with Refractory Seizure in Infant

Kim S, Kim JS, Kim DH, Lee JE, Kwon YS

Klinefelter syndrome a genetic disorder with various clinical manifestations. Neurological symptoms, such as seizures, are rarely reported with Klinefelter syndrome, and it response well to anti-epileptic drugs. A 5-month-old boy...
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Obesity Prevalence in Pediatric Headaches

Han AL, Shin CO, Cho KS, Bin JH, Jung MH, Suh BK

PURPOSE: Obesity and headache are two highly prevalent diseases both in childhood and adolescent. In this study, we assessed the prevalence of obesity in pediatric headaches patients in a single...
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Characteristics of Meningitis with or without Enterovirus

Cho WJ, Kwon YR, Cha BH

PURPOSE: Meningitis is an acute childhood infection caused by viral or bacterial infection. The purpose of the present study is to analyze the differences between enteroviral meningitis and non-enteroviral aseptic...
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Effects of Anticonvulsant Monotherapy on Bone Mineral Density in Children

Shin C, Lee NY, Han JY, Yoo IH, Eom TH, Bin JH, Kim YH, Chung SY, Lee IG

PURPOSE: The use of anticonvulsants can cause side effects such as reduction of bone mineral density, requiring attention in growing children. The aim of our study is to investigate the...
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Impact of Influenza Infection on Febrile Seizures: Clinical Implications

Jang HN, Lee EH

PURPOSE: Febrile seizures (FSs) are the most common type of seizure in the first 5 years of life and are frequently associated with viral infections. Influenza infection is associated with...
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Hemiplegic Migraine Presenting with Unilateral Facial Palsy: A case report

Yeon GM

Hemiplegic migraine (HM) is a rare subtype of migraine with aura and is accompanied by a fully reversible motor aura. HM can occur in two forms: familial or sporadic. Currently,...
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Impact of Weather on Prevalence of Febrile Seizures in Children

Woo JH, Oh SB, Yim CH, Byeon JH, Eun BL

PURPOSE: Febrile seizure (FS) is the most common type of seizure in children between 6 months to 5 years of age. A family history of febrile seizures can increase the...
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Association of Low Serum Ionized Magnesium Level with Fever-Triggered Seizures in Epileptic Children

Suh S, Kim K, Byeon JH, Eun SH, Eun BL, Kim GH

PURPOSE: Several studies have shown that magnesium plays an important role in modulating N-methyl-D-aspartate (NMDA)-related seizures by blocking NMDA ion channel receptors. Clinicians usually measure total serum magnesium levels instead...
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Convulsions with Noroviral Gastroenteritis in Children at a Single Center in Korea

Kang S, Lee HJ, Kim SH

PURPOSE: Viral gastroenteritis is a common disease in infants and children. Seizures can be associated with viral gastroenteritis as benign convulsions with mild gastroenteritis (CwG). After the development of the...
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EEG can Predict Neurologic Outcome in Children Resuscitated from Cardiac Arrest

Yang DH, Ha SG, Kim HJ

PURPOSE: Early prediction of prognosis of children resuscitated from cardiac arrest is a major challenge. We investigated the utility of electroencephalography (EEG) and laboratory studies for predicting of neurologic outcome...
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The Prognostic Factors Affecting the Occurrence of Subsequent Unprovoked Seizure in Patients Who Present with Febrile Seizure after 6 Years of Age

Lee HJ, Kim SH

PURPOSE: Few reports have described the prognostic factors affecting the occurrence of subsequent unprovoked seizure in patients who present with febrile seizure (FS) after 6 years of age. We investigated...
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Early Diagnosis of KBG Syndrome Using Diagnostic Exome Sequencing

Hong JH, Kim SH, Lee ST, Choi JR, Kang HC, Lee JS, Kim HD

KBG syndrome is a rare neurodevelopmental disorder characterized by intellectual disability, skeletal anomalies, short stature, craniofacial dysmorphism, and macrodontia. ANKRD11 gene mutation and 16q24.3 microdeletion have been reported to cause...
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Iron Deficiency Anemia: The Possible Risk Factor of Complex Febrile Seizure and Recurrence of Febrile Seizure

Lee CY, Lee NM, Yi DY, Yun SW, Lim IS, Chae SA

PURPOSE: A relationship between Febrile seizure (FS) and iron deficiency anemia (IDA) has been found in several studies. However, few studies have focused on the role of IDA in complex...
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Tuberous Sclerosis Complex with Crohn's Disease

Kim MH, Lee YJ, Kim JY, Yi YY, Kang JW

Tuberous sclerosis complex (TSC) is an autosomal dominant disorder caused by mutation of one of two genes, TSC1 (encoding hamartin, 9q34) and TSC2 (encoding tuberin, 16p13). It invades the central...
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Age-Based Characteristics of West Syndrome in Patients with Mitochondrial Disease

Choi YH, Baek MS, Na JH, Kang HC, Lee JS, Kim HD, Lee YM

PURPOSE: West syndrome is a severe form of age-specific epilepsy that typically affects infants younger than 2 years of age with mitochondrial disease. We aimed to examine age-specific characteristics of...
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Etiological Classification and Developmental Outcomes in Floppy Infants: A Single Tertiary Center Experience

Park JM, Choi YH, Lee HN, Chung HJ

PURPOSE: Floppy infants or congenital hypotonia indicates decreased muscle tone in infants secondary to abnormalities of the central or the peripheral nervous system, or both. Previous literature classified its causes...
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Transient Abnormalities on Magnetic Resonance Imaging after Absence Seizures

Yoo HW, Yoon L, Kim HY, Kwak MJ, Park KH, Bae MH, Lee Y, Nam SO, Kim YM

Magnetic resonance imaging (MRI) is recommended for patients with epileptic seizures to rule out an underlying focal lesion. However, abnormalities in idiopathic generalized epilepsy, including childhood absence epilepsy, cannot usually...
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