- Flow-Assisted Differential Diagnosis of Hemolytic Anemia with Spherocytosis: A Case Report
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Won DI
- KMID: 1781638
- Korean J Lab Med.
- 2010 Aug;30(4):339-344.
- doi: 10.3343/kjlm.2010.30.4.339
In patients with hemolytic anemia associated with spherocytosis, differential diagnosis has to be made whether the hemolysis is immune-mediated or of non-immune origin. We report a case of hereditary spherocytosis... -
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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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- A Case of Transient Aplastic Crisis Induced by Human Parvovirus Bl9 in Hereditary Spherocytosis
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Shin KS, Son BR, Lee DH
- KMID: 2146194
- Korean J Clin Pathol.
- 1997 Dec;17(6):928-933.
Human parvovirus B19 is a single-strand DNA virus which causes erythema infectlosum, arthralgia, aplastic crisis in patients with red cell defect, chronic anemia in immunocompromised patients, and fetal hydrops in... -
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- Coexistence of Gilbert Syndrome and Hereditary Spherocytosis in a Child Presenting with Extreme Jaundice
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Lee JH, Moon KR
- KMID: 2315504
- Pediatr Gastroenterol Hepatol Nutr.
- 2014 Dec;17(4):266-269.
- doi: 10.5223/pghn.2014.17.4.266
Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. It is characterized by intermittent episodes of jaundice in the absence of hepatocellular disease or hemolysis. Hereditary spherocytosis is... -
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- Cryohemolysis, erythrocyte osmotic fragility, and supplementary hematimetric indices in the diagnosis of hereditary spherocytosis
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Emilse LA, Cecilia H, MarÃa TM, Eugenia MM, Alicia IB, Lazarte SS
- KMID: 2414359
- Blood Res.
- 2018 Mar;53(1):10-17.
- doi: 10.5045/br.2018.53.1.10
BACKGROUND: Hereditary spherocytosis (HS) is a chronic hemolytic anemia characterized by microspherocytes in the peripheral blood and increased erythrocyte osmotic fragility (EOF). This study evaluated the cryohemolysis test (CHT); initial... -
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- Prolonged Extreme Thrombocytosis in a Postsplenectomy Patient with Hereditary Spherocytosis
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Park YM, Park J, Jo Y, Kim SH, Shin KC, Won IS, Sym SJ, Cho EK, Shin DB, Lee JH
- KMID: 2252116
- Korean J Hematol.
- 2009 Dec;44(4):298-303.
- doi: 10.5045/kjh.2009.44.4.298
We report a case of prolonged extreme reactive thrombocytosis in a post-splenectomy patient with hereditary spherocytosis. A 29-year-old female patient presented with gall stones detected incidentally by abdominal ultrasonography. Her... -
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- The Effect of Amphotericin B on Erythrocyte Volume and Cation Content
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Park YS, Solomon S
- KMID: 687738
- Yonsei Med J.
- 1977 Dec;18(2):114-122.
- doi: 10.3349/ymj.1977.18.2.114
The effects of amphotericin B, an antifungal antibiotic, on erythrocyte volume and cation permeability were investigated by measuring the hematocrit, cell volume, cation content, fragility and osmotic behavior in rat... -
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- A Case of Moyamoya Syndrome Associated with Hereditary Spherocytosis
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Kim JS, Yoon WS, Kim GM, Kim IS, Woo YJ, Lee JH
- KMID: 1961855
- J Korean Child Neurol Soc.
- 1998 Oct;6(1):125-132.
Moyamoya is a chronic cerebrovascular disease characterized by progressive stenosis or occlusion of the terminal parts of both intermal carotid arteries with telangiectatic vascular network of collateral circulation at the... -
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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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- Influences of Heat on Function and Morphology of Peripheral Blood Cells
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Choi JW, Nahm CH, Lee JW, Kim JJ, Kim SK, Pai SH
- KMID: 2146193
- Korean J Clin Pathol.
- 1997 Dec;17(6):912-927.
BACKGROUND: Heat-treated erythrocytes have been reported to be undergone fragmentation and microspherocytes transformation in vitro. However, the changes for enzyme activity of WBCs is not well known. The purpose of... -
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- A Case of Immune Hemolytic Anemia due to Autoantibodies Against C and e Antigens in a Patient with Paroxysmal Nocturnal Hemoglobinuria and Myelodysplastic Syndrome
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Park MJ, Seo YH, Park PW, Kim KH, Park SH, Jeong JH, Lee JH, Hong JS, Ahn JY
- KMID: 1440725
- Korean J Blood Transfus.
- 2012 Apr;23(1):78-83.
Antiglobulin test-negative hemolytic anemia, thrombophilia, and marrow failure, such as aplastic anemia and myelodysplastic syndrome - refractory anemia (MDS-RA), are the primary clinical manifestations of paroxysmal nocturnal hemoglobinuria (PNH). Here,... -
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- Two Korean Cases of Hereditary Spherocytosis Caused by Mutations in SLC4A1
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Cho H, Lee JW, Chung NG, Lee SE, Jang W, Kim M, Han K, Kim Y
- KMID: 2414133
- Lab Med Online.
- 2018 Jul;8(3):114-118.
- doi: 10.3343/lmo.2018.8.3.114
Hereditary spherocytosis (HS) is caused by mutations in the SPTA1, SPTB, ANK1, SLC4A1, and EPB42 genes, all of which encode erythrocyte membrane proteins. Mutations in SLC4A1, which encodes band 3... -
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- Erythrocyte Membrane Protein Alterations by SDS-PAGE and Underlying Clinical Heterogeneity in Hereditary Spherocytosis
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Yoo ES, Choi HS, Shin HY, Ahn HS, Lee YK, Cho HI
- KMID: 1979968
- Korean J Pediatr Hematol Oncol.
- 1997 Oct;4(2):261-272.
BACKGROUND: Hereditary spherocytosis(HS) is a clinically and biochemically very heterogeneous disorder The purpose of this study is to detect erythrocyte membrane protein abnormalities by SDS-PAGE and to investigate the frequency... -
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