- Benign convulsion with mild gastroenteritis
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Kang B, Kwon YS
- KMID: 2284104
- Korean J Pediatr.
- 2014 Jul;57(7):304-309.
- doi: 10.3345/kjp.2014.57.7.304
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... -
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- Comprehensive understanding of atrial septal defects by imaging studies for successful transcatheter closure
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Song J
- KMID: 2284103
- Korean J Pediatr.
- 2014 Jul;57(7):297-303.
- doi: 10.3345/kjp.2014.57.7.297
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... -
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- Asymptomatic maternal 3-methylcrotonylglycinuria detected by her unaffected baby's neonatal screening test
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Lee SH, Hong YH
- KMID: 2284108
- Korean J Pediatr.
- 2014 Jul;57(7):329-332.
- doi: 10.3345/kjp.2014.57.7.329
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... -
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- Prevalence of restless legs syndrome and sleep problems in Korean children and adolescents with attention deficit hyperactivity disorder: a single institution study
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Kwon S, Sohn Y, Jeong SH, Chung US, Seo H
- KMID: 2284106
- Korean J Pediatr.
- 2014 Jul;57(7):317-322.
- doi: 10.3345/kjp.2014.57.7.317
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... -
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- Atypical teratoid rhabdoid brain tumor in an infant with ring chromosome 22
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Cho EH, Park JB, Kim JK
- KMID: 2284109
- Korean J Pediatr.
- 2014 Jul;57(7):333-336.
- doi: 10.3345/kjp.2014.57.7.333
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... -
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- Prader-Willi syndrome: a single center's experience in Korea
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Kim YJ, Cheon CK
- KMID: 2284105
- Korean J Pediatr.
- 2014 Jul;57(7):310-316.
- doi: 10.3345/kjp.2014.57.7.310
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... -
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- Articulation error of children with adenoid hypertrophy
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Eom TH, Jang ES, Kim YH, Chung SY, Lee IG
- KMID: 2284107
- Korean J Pediatr.
- 2014 Jul;57(7):323-328.
- doi: 10.3345/kjp.2014.57.7.323
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... -
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