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A Case of Neutrophilic Eccrine Hidradenitis

Kim JW, Kim KS, Kim CH, Oh CW

  • KMID: 2303227
  • Korean J Dermatol.
  • 2000 Aug;38(8):1121-1123.
Neutrophilic eccrine hidradenitis(NEH) is a self-limited inflammatory dermatosis primarily induced by chemotherapeutic agents. The pathogenesis and possible cause of NEH remain unknown. NEH may represent as a reaction pattern to...
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Colonic Angioectasia in an Adolescent Boy with Hoyeraal-Hreidarsson on Long-Term Anabolic Steroid Therapy

Khalaf R, Cuffari C

Androgen therapy has proven efficacy in treating patients with bone marrow failure who are not candidates for bone marrow transplantation. Herein, we report on a case of colonic angioectasia secondary...
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Dyskeratosis Congenita in a Girl

Yi JS, Kook H, Paik HJ, Kim SY, Choi IS, Kim SJ, Sohn KR, Nam HS, Hwang TJ

  • KMID: 2278307
  • Korean J Pediatr Hematol Oncol.
  • 2003 Oct;10(2):293-298.
Dyskeratosis congenita (DC) is a rare genetic disorder encompassing abnormal skin pigmentation, dystrophic nails, leukoplakia of mucous membranes and others. Bone marrow failure is the cause of early mortality. Moreover,...
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Direct and Indirect Effects of Androgens on Survival of Hematopoietic Progenitor Cells In Vitro

Kim SW, Hwang JH, Cheon JM, Park NS, Park SE, Park SJ, Yun HJ, Kim S, Jo DY

Androgens remain a common treatment for certain type of anemia, based upon its myelostimulating effects; however, it has not been established whether androgens affect apoptosis of hematopoietic progenitor cells (HPCs)....
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Reassessment of a Dup (1)(q21q32), Trp (1)(q21q32) in a Case of Myelodysplastic Syndrome by CGH (Comparative Genomic Hybridization)

Choi JR, Lee KA, Park Q, Song KS, Ko YW

  • KMID: 1532660
  • Korean J Hematol.
  • 1998 May;33(1):110-116.
Acquired partial duplication or triplication of the long arm of human chromosome 1 has been observed rarely in myelodysplastic syndrome (MDS). We describe a dup (1)(q21q32), trp (1)(q21q32) in a...
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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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A Clinical Study of Fanconi's Anemia

Cho SH, Kook H, Kim GM, Yoon WS, Cho TH, Hwang TJ

  • KMID: 2072456
  • Korean J Pediatr Hematol Oncol.
  • 1997 Apr;4(1):70-77.
BACKGROUND: Fanconi's anemia(FA) is an autosomal recessive disease characterized by aplastic anemia and congenital malformations. As up to 30% of patients have no physical stigmata, the modern diagnosis of FA...
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Aplastic Anemia Associated with Stomach

Hahn JS, Kim DY, Nam DK, Lee YS, Lee SJ, Ko YW, Cho CH

Herein is presented a case of aplastic anemia associated with adenocarcinoma of the stomach which seem- ed to be coincidental. A 52 year-old man was admitted with a 3...
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Improvement in Erythropoieis-stimulating Agent-induced Pure Red-cell Aplasia by Introduction of Darbepoetin-alpha When the Anti-erythropoietin Antibody Titer Declines Spontaneously

Lee H, Yang J, Kim H, Kwon JW, Oh KH, Joo KW, Kim YS, Ahn C, Han JS, Kim S

Anti-erythropoietin antibodies usually cross-react with all kinds of recombinant erythropoietins; therefore, erythropoiesis-stimulating agent (ESA)-induced pure red-cell aplasia (PRCA) is not rescued by different ESAs. Here, we present a case of...
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