Korean Journal of Pediatrics

Title Publication Date Language Citations
B-type natriuretic peptide may have a role in the management of patent ductus arteriosus2018/01/01English
Sudden unexpected cardio-respiratory arrest after venipuncture in children2018/01/01English
Successful treatment of tubulointerstitial nephritis and uveitis with steroid and azathioprine in a 12-year-old boy2016/01/01English
Chromosome 11q13 deletion syndrome2016/01/01English
Hashimoto thyroiditis with an unusual presentation of cardiac tamponade in Noonan syndrome2016/01/01English
A novel mutation ofABCC8gene in a patient with diazoxide-unresponsive congenital hyperinsulinism2016/01/01English
Acute gastritis associated with Epstein-Barr virus infection in a child2016/01/01English
Ictal sinus pause and myoclonic seizure in a child2016/01/01English
A novel mutation ofCLCNKBin a Korean patient of mixed phenotype of Bartter-Gitelman syndrome2016/01/01English
1p36 deletion syndrome confirmed by fluorescencein situhybridization and array-comparative genomic hybridization analysis2016/01/01English
A pediatric case of idiopathic Harlequin syndrome2016/01/01English
Eosinophilic gastroenteritis in an 18-year-old male with prolonged nephrotic syndrome2016/01/01English
Interstitial deletion of 5q33.3q35.1 in a boy with severe mental retardation2016/01/01English
Endovascular stenting of tracheoinnominate fistula after tracheostomy in a 14-year-old boy2016/01/01English
Familial Mediterranean fever presenting as fever of unknown origin in Korea2016/01/01English
Esthesioneuroblastoma in a boy with 47, XYY karyotype2016/01/01English
Maternal 3-methylcrotonyl-coenzyme A carboxylase deficiency with elevated 3-hydroxyisovalerylcarnitine in breast milk2016/01/01English
Compound heterozygous mutations ofACADSgene in newborn with short chain acyl-CoA dehydrogenase deficiency: case report and literatures review2016/01/01English
Congenital miliary tuberculosis in an 18-day-old boy2016/01/01English
Paroxysmal kinesigenic dyskinesia in a patient with aPRRT2mutation and centrotemporal spike discharges on electroencephalogram: case report of a 10-year-old girl2016/01/01English
Glucose transport 1 deficiency presenting as infantile spasms with a mutation identified in exon 9 ofSLC2A12016/01/01English
A rare case of dysembryoplastic neuroepithelial tumor combined with encephalocraniocutaneous lipomatosis and intractable seizures2016/01/01English
Idiopathic midaortic syndrome with malignant hypertension in 3-year-old boy2016/01/01English
Concomitant occurrence of Turner syndrome and growth hormone deficiency2016/01/01English
Posterior reversible encephalopathy syndrome caused by presumed Takayasu arteritis2016/01/01English
Granular cell tumor of the esophagus in an adolescent2016/01/01English
A novelBTKgene mutation, c.82delC (p.Arg28 Alafs*5), in a Korean family with X-linked agammaglobulinemia2016/01/01English
A neonate with Joubert syndrome presenting with symptoms of Horner syndrome2016/01/01English
A nonsensePAX6mutation in a family with congenital aniridia2016/01/01English
Commentary on “Megalencephaly-capillary malformation-polymicrogyria syndrome: the first case report in Korea”2018/01/01English