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A Case of Brain Stem Glioma Responded to Tamoxifen after Relapse with Chemotherapy and Radiotherapy

Choi SW, Nam SG

  • KMID: 1535342
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):353-357.
Tamoxifen is an oral triphenylethylene antiestrogen that has been used for breast cancer, but also inhibits protein kinase C(PKC) in a minority of malignant gliomas. Tamoxifen was administered orally in...
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Erythroleukemia Related to Chronic Ebstein-Barr Virus Infection

Yoon CG, Park SY, Chung WY, Lee SY, Lee YH

  • KMID: 1535341
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):346-352.
It is well known that the Ebstein-Barr virus causes not only infectious mononucleosis in the most cases, but also occasionally causes a variety of hematologic disorders such as anemia (hemolytic...
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A Case of Wiskott-Aldrich Syndrome Misdiagnosed as Chronic Idiopathic Thrombocytopenia

Choi HK, Park CY, Sohn JH

  • KMID: 1535340
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):340-345.
Wiskott-Aldrich syndrome is a rare inheritable disease. Though there are many reported cases in the world, there are only 3 reported cases in Korea. We experienced a 7 years old...
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A Case of Plasma Cell Type Giant Lymph Node Hyperplasia (Castleman's Disease)

Lee JY, Lee SY, Jung JW, Kim MK, Park KH, Soh DM

  • KMID: 1535339
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):333-339.
Castleman's disease was first described in 1956 in a group of patients with localized mediastinal lymph node enlargement characterized by hyperplasia of lymphoid follicles and marked capillary proliferation with endothelial...
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A Case Report of Idiopathic Myelofibrosis with Down Syndrome

Lim JY, Woo CW, Lee JH, Lee KC, Whang MW, Cho YJ

  • KMID: 1535338
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):328-332.
No abstract available.
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Infant with Fanconi Anemia Presenting with Myelodysplastic Syndrome

Cho TH, Kook H, Ryu NE, Kim CJ, Lee JH, Hwang TJ

  • KMID: 1535337
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):322-327.
PURPOSE: Fanconi anemia(FA) is a rare autosomal recessive disorder characterized by progressive bone marrow failure and congenital malformations. Patients with FA have aplastic anemia(> 90%), leukemia(10~15%), myelodysplasia(5%) and liver(5%) and...
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The Study on Administration of High-Dose Methotrexate in Children with Osteosarcoma

Kim EA, Im HJ, Lee H

  • KMID: 1535336
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):314-321.
PURPOSE: We investigated serum levels of MTX and accompanying organic toxicities after administration of High-Dose Methotrexate (HDMTX). METHODS: We reviewed a total of 42 courses of HDMTX administration in 6 patients...
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The Combined Therapy of Peripheral Primitive Neuroectodermal Tumor in Childhood

Jang PS, Lee JA, Choi Y, Han HJ, Choi HS, Shin HY, Ahn HS

  • KMID: 1535335
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):304-313.
PURPOSE: A review of the literature for patients with peripheral primitive neuroectodermal tumor (PPNET; peripheral neuroepithelioma) suggests that the outcome is usually poor. We performed a retrospective study to emphasize...
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Loss of Heterozygosity Studies on Chromosome 9, 22 and 17p in 12 Various Pediatric Brain Tumors

Jung HL, Lau CC

  • KMID: 1535334
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):293-303.
PURPOSE: The normal function of tumor suppressor genes is thought to be related to their ability to regulate cell proliferation and the loss of such function presumably leads to malignant...
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Adriamycin Induces Apoptosis of Human Myeloid Leukemic U937 Cells via Activation of Caspase-3 and cJun-N Terminal Kinase1(JNK1)/Stress Activated Protein Kinase(SAPK)

Choi DY, Jung BH, So HS

  • KMID: 1535333
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):285-292.
PURPOSE: Recent studies indicate that widely used chemotherapeutic agents induce apoptosis in susceptible cells. One of the effector arms in this cell death pathway is composed of cysteine proteases belonging...
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Clinical Feature of von Willebrand Disease

Lee KS, Choi EJ

  • KMID: 1535332
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):278-284.
PURPOSE: Although von Willebrand disease is the most frequent hereditary hemorrhagic disorder. Its biological characteristics make some difficulties in diagnosing this common disease, so careful individual history taking and laboratory...
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Comparison of Combined Immune Suppression, Bone Marrow Transplantation and Androgen Treatment in Childhood Severe Aplastic Anemia

Hwang MJ, Kook H, Kim CJ, Park HJ, Kim SY, Park A, Hwang TJ

  • KMID: 1535331
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):266-277.
PURPOSE: The purpose of this study is to compare treatment response and survival according to treatment modalities, such as allogeneic bone marrow transplantation (BMT), combined immunosuppression and supportive care, and...
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Chronic Childhood Idiopathic Thrombocytopenic Purpura: Long-term Follow-up

Yum DH, Im HJ, Lee H

  • KMID: 1535330
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):260-265.
PURPOSE: The purpose of this study was to evaluate the spontaneous remission rate in children with chronic ITP. METHODS: The medical records of 21 patients diagnosed with chronic ITP and followed...
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Gene Therapy of Cancer by the Inhibition of Transcription and Expression

Hwang PH, Yi HK

  • KMID: 1535329
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):250-259.
No abstract available.
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Umbilical Cord Blood Stem Cell Transplantation

Shin HY

  • KMID: 1535328
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):245-249.
No abstract available.
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Hematopoietic Stem Cell Transplantation in Inborn Error of Metabolism

Cho B

  • KMID: 1535327
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):240-244.
No abstract available.
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Neuropeptide Effects of Hematopoiesis

Park SK

  • KMID: 1535326
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):235-239.
No abstract available.
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