Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

PUBLICATION DATE

12 results
Display

Reticulocytosis in screen-printing workers exposed to 2-butoxyethanol and 2-ethoxyethanol

Song SH, Kang SK, Choi WJ, Kwak KM, Lee DH, Kang DY, Lee SH

BACKGROUND: Studies on the hematologic toxicity of ethylene glycol ethers in humans are limited. Therefore, the aim of this study was to examine the association between exposure to solvents (containing...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Acquired Pure Red Cell Aplasia following Autoimmune Hemolytic Anemia in Systemic Lupus Erythematosus

Kim MH, Choi JY, Lee SM, Ahn SW, Jung SM, Kim H, Won HS

Pure red cell aplasia (PRCA) is a rare hematological disorder characterized by severe normochromic normocytic anemia and reticulocytopenia due to erythroid progenitor depletion in an otherwise normal bone marrow. Autoimmune...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Red Cell Depletion from the Bone Marrow Aspirates for the ABO Incompatible Transplantation by Apheresis Separations

Choi KH, Sung HJ, Lee WH, Kim HO, Lyu CJ, Min YH

  • KMID: 2143333
  • Korean J Hematol.
  • 2001 Nov;36(4):318-323.
BACKGROUND: Allogeneic bone marrow transplantation across ABO incompatibility barriers may result in immune mediated hemolysis. Hemolysis may be avoided by RBC depletion from the graft. In vitro graft manipulations carry...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Pseudoreticulocytosis in a Case of Myelodysplastic Syndrome

Kang JO, Lee JS, Kim JY, Kim SH, Park CW, Park TS, Jeong YT, Chung JS, Lee EY, Cho GJ

  • KMID: 1832124
  • Korean J Hematol.
  • 2001 May;36(2):176-179.
Myelodysplastic syndrome (MDS) is a group of hematopoietic disorders characterized by ineffective hematopoiesis and peripheral cytopenia associated with dysplastic hypercellular marrow. Anemia is a frequent finding and reticulocytes are usually...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Myelodysplastic Syndrome with Delayed Maturation of Reticulocytes: A Report of Three Cases

Yang SE, Park JS, Seo EZ, Chi HS

  • KMID: 2089491
  • Korean J Clin Pathol.
  • 1998 Jun;18(2):126-129.
Anemia in myelodysplastic syndrome (MDS) is accompanied by reticulocytopenia in most patients. Reticulocytosis, when present, is generally less than appropriate to the degree of anemia and rarely exceeds 10%. In...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Coexistence with Myelodysplastic Syndrome and Paroxysmal Nocturnal Hemoglobinuria: Confirmed by Reticulocytes Survival Test and Glycosylphosphatidylinositol (GPI)-linked Protein Test

Lim JH, Kim Y, Kim DW, Jin JY, Han CW, Han K, Shim SI, Kim CC

  • KMID: 2038504
  • Korean J Hematol.
  • 1997 Nov;32(3):465-469.
A patient presenting paroxysmal nocturnal hemoglobinuria (PNH) cloned cells in the course of myelodysplastic syndrome (MDS) with reticulocytosis is described. The bone marrow biopsy demonstrated erythroid hyperplasia and moderate dysplasia....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Comparison Study of Reticulocyte Enumeration by H*3 RTX(TM), FACScan(TM), and Manual Counting

Lee JW, Choi HS, Song KE, Suh JS, Lee WK, Kim JS, Kim BW

  • KMID: 2225570
  • Korean J Clin Pathol.
  • 1997 Apr;17(2):218-229.
BACKGROUND: Reticulocyte counts provide clinically useful informations and the most widely used method for counting reticulocytes is a manual microscopic procedure. Although manual method is inexpensive and relatively simple to...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Splenectomy in Hereditary Spherocytosis in Childhood

Heo YS, Kim CS, Do BS, Suh BY, Hah JO

Among the erythrocyte membrane defects, hereditary spherocytosis is the most common. The erythrocyte membrane defect results from a deficiency of spectrin, the most important structural protein in red cell. Hereditary spherocytosis...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Clinical evaluation on 5 cases of lead Poisoning

Lee JM, Lee HW, Hyun MS, Chung MK, Shim BS, Lee HW

5 cases of lead poisoning were investigated clinically. Of the 5 patients, 4 were male and 1 was female. The causes of lead poisoning in 3 cases were ingestion of herb drug...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Congenital Syphilis: Hematologic Findings of Early Congenital Syphilis

Lee JB, Kim DK, Koh YJ

  • KMID: 1679445
  • Korean J Dermatol.
  • 1985 Dec;23(6):759-763.
A retrospective study was made of the previous medical records of 47 infants with congenital syphilis born from mothers with untreated syphilis at Severance Hospital, Yonsei University College of Medicine...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Prednisolone-responsive Malignant Osteopetrosis: a case reveiw

Bae CW, Kang HS, Min JS, Kang SC, Lee SW

  • KMID: 1699493
  • J Korean Pediatr Soc.
  • 1982 May;25(5):512-517.
The authors presented a 17 months old female with malignant osteopetrosis, who was admitted to the Pediatric Department of Kyung Hee University Hospital on May, 1981 because of epistaxis and...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2022 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr