- A Case of Pinealoblastoma with Consequently Discovered Wilms Tumor
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Kwak GY, Bae SY, Lee SY, Chung SY, Kang JH, Park IS, Suh HJ, Jeong DC
- KMID: 2049214
- Clin Pediatr Hematol Oncol.
- 2006 Apr;13(1):66-71.
The co-occurrence of embryonal tumors originating in the kidney and the brain are very rare. A 2 months old girl presented with a significantly increased head circumference. She received tumor... -
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- A Case of Congenital Acute Lymphoblastic Leukemia
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Hong SP, Choe BK, Kim HS, Kim CS, Lee SL, Ha JS
- KMID: 2049213
- Clin Pediatr Hematol Oncol.
- 2006 Apr;13(1):60-65.
Congenital leukemia, which occurs before 4 weeks of life, is distinguished from that occurring in childhood. It is often associated with MLL gene rearrangement and its prognosis is poor. Chemotherapy... -
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- Central Diabetes Insipidus as a Manifestation of Langerhans Cell Histiocytosis: Report of 3 Cases with Literature Review
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Han DK, Kook H, Baek HJ, Song ES, Kang HS, Kim MJ, Kim SJ, Kim SH, Kim CJ, Hwang TJ
- KMID: 2049215
- Clin Pediatr Hematol Oncol.
- 2006 Apr;13(1):72-79.
Central diabetes insipidus (CDI) is the most common manifestation of central nervous system involvement in Langerhans cell histiocytosis (LCH). Therefore, in patients with endocrinologically proven CDI, a comprehensive diagnostic evaluation... -
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- A Case of Concurrent Acute Myelogenous Leukemia and Retroperitoneal Teratoma in an Infant
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Park SS, Park HS, Lee CH, Lee EY, Lim YT
- KMID: 2049212
- Clin Pediatr Hematol Oncol.
- 2006 Apr;13(1):55-59.
Most hematologic malignancies occurring in a patient with a malignant solid tumor are secondary leukemia developing as complications after chemotherapy or radiotherapy. On the other hand, it is very rare... -
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- Anemia of Chronic Disease in Children: Focus on Etiologic Diagnosis
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Ye GY, Kwon OG, Kim HM
- KMID: 2049209
- Clin Pediatr Hematol Oncol.
- 2006 Apr;13(1):32-38.
PURPOSE: The purpose of this study was to find out the clinical characteristics and to establish the diagnostic work-up of anemia of chronic disease (ACD) according to the underlying causes... -
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- Alteration of Lymphocyte after Cessation of Anticancer Therapy in Patients with Malignancy
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Yang SW, Jeon IS, Lee JB, Son DW
- KMID: 2049210
- Clin Pediatr Hematol Oncol.
- 2006 Apr;13(1):39-45.
PURPOSE: The immunologic function after cessation of anticancer therapy is usually compromised, thus predisposing patients to infections, sometimes fatal. The number and subtype of lymphocytes, which play the central role... -
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- Improved Survival in Neuroblastoma by Autologous Peripheral Blood Stem Cell Transplantation: A Single Institution Experience
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Kim JY, Baek HJ, Han DK, Sung JS, Nam TK, Yoon MS, Kook H, Hwang TJ
- KMID: 2049207
- Clin Pediatr Hematol Oncol.
- 2006 Apr;13(1):9-21.
PURPOSE: Neuroblastoma is the most common extracranial solid tumor of childhood, and its outcome in advanced diseases has been very poor. We evaluated the treatment outcome and prognostic factors in... -
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- Differentiation of Endothelial Progenitor Cells from Cord Blood by Ex Vivo Expansion
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Yoo ES, Gil TY, Lee SJ
- KMID: 2049211
- Clin Pediatr Hematol Oncol.
- 2006 Apr;13(1):46-54.
PURPOSE: Endothelial progenitor cells (EPCs) play a significant role in neovascularization of ischemic tissues and in re-endothelialization of injured blood vessels and hold promise for therapeutic neovascularization. The purpose of... -
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- A Clinical Characteristics and Prognosis in Children of Acute Lymphoblastic Leukemia with Hyperleukocytosis
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Park JA, Park SS, Lim YT
- KMID: 2049206
- Clin Pediatr Hematol Oncol.
- 2006 Apr;13(1):1-8.
PURPOSE: Hyperleukocytosis combined with acute lymphoblastic leukemia (ALL) is associated with early morbidity and mortality because leukostasis interferes with the blood flow by leukocytes within the microcirculation and can result... -
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- The Aplastic Crisis of Hereditary Spherocytosis Due to Parvovirus B19 Infection
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Choi HJ, Lee JH, Lee KS
- KMID: 2049208
- Clin Pediatr Hematol Oncol.
- 2006 Apr;13(1):22-31.
PURPOSE: Hereditary spherocytosis (HS) is the commonest cause of inherited hemolytic anemia in Korea. In hereditary spherocytosis patients, parvovirus B19 infection causes transient severe anemia, so called aplastic crisis. This... -
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