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A Case of Pinealoblastoma with Consequently Discovered Wilms Tumor

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

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

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

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

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

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

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

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

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

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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