- Diagnosis of incomplete Kawasaki disease
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Yu JJ
- KMID: 2284313
- Korean J Pediatr.
- 2012 Mar;55(3):83-87.
- doi: 10.3345/kjp.2012.55.3.83
Several authors suggested that the clinical characteristics of incomplete presentation of Kawasaki disease are similar to those of complete presentation and that the 2 forms of presentation are not separate... -
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- A case of Hashimoto's encephalopathy presenting with seizures and psychosis
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Lee MJ, Lee HS, Hwang JS, Jung DE
- KMID: 2284318
- Korean J Pediatr.
- 2012 Mar;55(3):111-113.
- doi: 10.3345/kjp.2012.55.3.111
Hashimoto's encephalopathy (HE) is a rare, poorly understood, autoimmune disease characterized by symptoms of acute or subacute encephalopathy associated with increased anti-thyroid antibody levels. Here, we report a case of... -
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- A case of partial trisomy 3p syndrome with rare clinical manifestations
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Han DH, Chang JY, Lee WI, Bae CW
- KMID: 2284317
- Korean J Pediatr.
- 2012 Mar;55(3):107-110.
- doi: 10.3345/kjp.2012.55.3.107
Partial trisomy 3p results from either unbalanced translocation or de novo duplication. Common clinical features consist of dysmorphic facial features, congenital heart defects, psychomotor and mental retardation, abnormal muscle tone,... -
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- Epidemiology of astrovirus infection in children
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Jeong HS, Jeong A, Cheon DS
- KMID: 2284312
- Korean J Pediatr.
- 2012 Mar;55(3):77-82.
- doi: 10.3345/kjp.2012.55.3.77
Human astrovirus (HAstV) is a major cause of acute diarrhea among children, resulting in outbreaks of diarrhea and occasionally hospitalization. Improved surveillance and application of sensitive molecular diagnostics have further... -
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- Hematopoietic stem cell transplantation in children with acute leukemia: similar outcomes in recipients of umbilical cord blood versus marrow or peripheral blood stem cells from related or unrelated donors
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Yi ES, Lee SH, Son MH, Kim JY, Cho EJ, Lim SJ, Cheuh HW, Yoo KH, Sung KW, Koo HH
- KMID: 2284315
- Korean J Pediatr.
- 2012 Mar;55(3):93-99.
- doi: 10.3345/kjp.2012.55.3.93
PURPOSE: This study compared outcomes in children with acute leukemia who underwent transplantations with umbilical cord blood (UCB), bone marrow, or peripheral blood stem cells from a human leukocyte antigen... -
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- Outcome of allogeneic hematopoietic stem cell transplantation for childhood acute lymphoblastic leukemia in second complete remission: a single institution study
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Lee EJ, Han JY, Lee JW, Jang PS, Chung NG, Jeong DC, Cho B, Kim HK
- KMID: 2284316
- Korean J Pediatr.
- 2012 Mar;55(3):100-106.
- doi: 10.3345/kjp.2012.55.3.100
PURPOSE: The survival rate for childhood acute lymphoblastic leukemia (ALL) has improved significantly. However, overall prognosis for the 20 to 25% of patients who relapse is poor, and allogeneic hematopoietic... -
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- A study of the relationship between clinical phenotypes and plasma iduronate-2-sulfatase enzyme activities in Hunter syndrome patients
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Lee OJ, Kim SJ, Sohn YB, Park HD, Lee SY, Kim CH, Ko AR, Yook YJ, Lee SJ, Park SW, Kim SH, Cho SY, Kwon EK, Han SJ, Jin DK
- KMID: 2284314
- Korean J Pediatr.
- 2012 Mar;55(3):88-92.
- doi: 10.3345/kjp.2012.55.3.88
PURPOSE: Mucopolysaccharidosis type II (MPS II or Hunter syndrome) is a rare lysosomal storage disorder caused by iduronate-2-sulfatase (IDS) deficiency. MPS II causes a wide phenotypic spectrum of symptoms ranging... -
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