Skip Navigation
Skip to contents
Filter

ARTICLE TYPE

PUBLICATION DATE

7 results
Display

Benign convulsion with mild gastroenteritis

Kang B, Kwon YS

Benign convulsion with mild gastroenteritis (CwG) is a type of afebrile seizure that occurs in children. CwG is defined as a convulsion in a previously healthy child with no known...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Comprehensive understanding of atrial septal defects by imaging studies for successful transcatheter closure

Song J

Transcatheter closure of atrial septal defects has become a popular procedure. The availability of a preprocedural imaging study is crucial for a safe and successful closure. Both the anatomy and...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Asymptomatic maternal 3-methylcrotonylglycinuria detected by her unaffected baby's neonatal screening test

Lee SH, Hong YH

3-methylcrotonyl-coenzyme A carboxylase (3MCC) deficiency is an autosomal recessive disorder in which leucine catabolism is hampered, leading to increased urinary excretion of 3-methylcrotonylglycine. In addition, 3-hydroxyisovalerylcarnitine levels increase in the...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Prevalence of restless legs syndrome and sleep problems in Korean children and adolescents with attention deficit hyperactivity disorder: a single institution study

Kwon S, Sohn Y, Jeong SH, Chung US, Seo H

PURPOSE: Attention deficit hyperactivity disorder (ADHD) is a common disorder in school-aged children. Patients with restless legs syndrome (RLS) often present with ADHD symptoms and vice versa. This study was...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Atypical teratoid rhabdoid brain tumor in an infant with ring chromosome 22

Cho EH, Park JB, Kim JK

Reports of constitutional ring chromosome 22, r(22) are rare. Individuals with r(22) present similar features as those with the 22q13 deletion syndrome. The instability in the ring chromosome contributes to...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Prader-Willi syndrome: a single center's experience in Korea

Kim YJ, Cheon CK

PURPOSE: Prader-Willi syndrome (PWS) is a complex genetic disorder that results from the lack of paternally expressed genes in the chromosome 15q11-q13 region. This study was performed to delineate the...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Articulation error of children with adenoid hypertrophy

Eom TH, Jang ES, Kim YH, Chung SY, Lee IG

PURPOSE: Adenoid hypertrophy is a physical alteration that may affect speech, and a speech disorder can have other negative effects on a child's life. Airway obstruction leads to constricted oral...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr