- Myelodysplastic Syndrome with Delayed Maturation of Reticulocytes: A Report of Three Cases
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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... -
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- Pseudoreticulocytosis in a Case of Myelodysplastic Syndrome
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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... -
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- Congenital Syphilis: Hematologic Findings of Early Congenital Syphilis
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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... -
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- A Case of Coexistence with Myelodysplastic Syndrome and Paroxysmal Nocturnal Hemoglobinuria: Confirmed by Reticulocytes Survival Test and Glycosylphosphatidylinositol (GPI)-linked Protein Test
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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.... -
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- Reticulocytosis in screen-printing workers exposed to 2-butoxyethanol and 2-ethoxyethanol
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Song SH, Kang SK, Choi WJ, Kwak KM, Lee DH, Kang DY, Lee SH
- KMID: 2455032
- Ann Occup Environ Med.
- 2017 ;29(1):54.
- doi: 10.1186/s40557-017-0210-z
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... -
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- Clinical evaluation on 5 cases of lead Poisoning
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Lee JM, Lee HW, Hyun MS, Chung MK, Shim BS, Lee HW
- KMID: 2377228
- Yeungnam Univ J Med.
- 1989 Dec;6(2):29-38.
- doi: 10.12701/yujm.1989.6.2.29
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... -
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- Acquired Pure Red Cell Aplasia following Autoimmune Hemolytic Anemia in Systemic Lupus Erythematosus
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Kim MH, Choi JY, Lee SM, Ahn SW, Jung SM, Kim H, Won HS
- KMID: 2218782
- Korean J Med.
- 2016 Jun;90(6):554-558.
- doi: 10.3904/kjm.2016.90.6.554
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... -
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- Comparison Study of Reticulocyte Enumeration by H*3 RTX(TM), FACScan(TM), and Manual Counting
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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... -
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- Splenectomy in Hereditary Spherocytosis in Childhood
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Heo YS, Kim CS, Do BS, Suh BY, Hah JO
- KMID: 2352262
- Yeungnam Univ J Med.
- 1994 Jun;11(1):42-48.
- doi: 10.12701/yujm.1994.11.1.42
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... -
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- Prednisolone-responsive Malignant Osteopetrosis: a case reveiw
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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... -
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- Red Cell Depletion from the Bone Marrow Aspirates for the ABO Incompatible Transplantation by Apheresis Separations
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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... -
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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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