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Idiopathic hypercalciuria in children with hematuria

Koo KY, Lee JH, Ko CW, Koo JH

  • KMID: 1694687
  • Korean J Nephrol.
  • 1992 Oct;11(3):248-252.
No abstract available.
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The First Case of Familial Mediterranean Fever Associated with Renal Amyloidosis in Korea

Koo KY, Park SJ, Wang JY, Shin JI, Jeong HJ, Lim BJ, Lee JS

Familial Mediterranean fever (FMF) is an auto-inflammatory disease characterized by periodic episodes of fever and recurrent polyserositis. It is caused by a dysfunction of pyrin (or marenostrin) as a result...
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Postnatal changes of creatine kinase and isoenzyme activities in normal and asphyxiated newborns

Koo KY, Heo NG, Kim HM

  • KMID: 1945903
  • J Korean Pediatr Soc.
  • 1993 Sep;36(9):1219-1226.
This study was conducted to evaluate the postnatal changes of serum creatine kinase (CK) and its isoenzymes in normal and asphyxiated newborns. In normal newborns total CK, CK-MM and CK-MB...
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A Korean Patient with Kniest Syndrome associated with Lipomeningomyelocele

Min HW, Koo KY, Lee CH, Yang JY, Lee JS

Kniest syndrome (OMIM #156550) is a rare autosomal dominant disorder caused by a dysfunction of type II collagen, which is encoded by the COL2A1 gene (OMIM +120140) mapped to chromosome...
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A case of postoperative nasopharyngeal reflux associated with retropharyngeal lymphangioma in newborn infant

Koo KY, Lee JS, Lee SM, Park MS, Namgung R, Park KI, Lee C, Yoon CS, Jung WH, Choi HS

Lymphangioma is a rare benign congenital tumor of the lymphatic system, which is commonly diagnosed before 2 years of age. In the natronal report, cystic lymphangioma was usually reported as...
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Clinical experience of therapeutic effect of peritoneal drainage on intestinal perforation in preterm infants

Lee JS, Koo KY, Lee SM, Park MS, Park KI, Namgung R, Lee C, Choi SH

PURPOSE: To analyze and compare various cases in which peritoneal drainage was used as the primary treatment method in preterm infants with intestinal perforation. METHODS: Among the preterm infants of...
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Isolated Cerebellar Variant of Adrenoleukodystrophy with a de novo Adenosine Triphosphate-Binding Cassette D1 (ABCD1) Gene Mutation

Kang JW, Lee SM, Koo KY, Lee YM, Nam HS, Quan Z, Kang HC

X-linked adrenoleukodystrophy (X-ALD) shows a wide range of phenotypic expression, but clinical presentation as an isolated lesion of the cerebellar white matter and dentate nuclei has not been reported. We...
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Genetic and Epileptic Features in Rett Syndrome

Kim HJ, Kim SH, Kim HD, Lee JS, Lee YM, Koo KY, Lee JS, Kang HC

PURPOSE: Rett syndrome is a severe neurodevelopmental disorder in females. Most have mutations in the methyl-CpG-binding protein 2 (MECP2) gene (80-90%). Epilepsy is a significant commonly accompanied feature in Rett...
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Effect of severe neonatal morbidities on long term outcome in extremely low birthweight infants

Koo KY, Kim JE, Lee SM, Namgung R, Park MS, Park KI, Lee C

PURPOSE: To assess the validity of individual and combined prognostic effects of severe bronchopulmonary dysplasia (BPD), brain injury, retinopathy of prematurity (ROP), and parenteral nutrition associated cholestasis (PNAC). METHODS: We retrospectively...
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