- A new paradigm in the diagnosis of hereditary hemolytic anemia
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Jung HL
- KMID: 2172867
- Blood Res.
- 2013 Dec;48(4):237-239.
- doi: 10.5045/br.2013.48.4.237
No abstract available. -
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- A Case of Congenital Nonspherocytic Hemolytic Anemia
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Kim TS, Jeon SB, Pyun BY
- KMID: 1676260
- J Korean Pediatr Soc.
- 1985 Jun;28(6):597-603.
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- A Case of Congenital Hemolytic Anemia of Unknown Cause Combined with Gilbert's Syndrome
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Lim JW, Choi JH, Nam YH, Seo IS, Yoon SM, Koo MS
- KMID: 1485159
- Korean J Hematol.
- 2008 Mar;43(1):58-61.
- doi: 10.5045/kjh.2008.43.1.58
Congenital hemolytic anemia is mainly developed due to intrinsic defects of erythrocytes, but in some cases the cause of hemolytic anemia is unclear. Gilbert's syndrome shows mild, chronic unconjugated hyperbilirubinemia... -
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- Glucose-6-phosphate Dehydrogenase Deficiency
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Lee JM
- KMID: 2168913
- Clin Pediatr Hematol Oncol.
- 2015 Apr;22(1):1-7.
- doi: 10.15264/cpho.2015.22.1.1
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzyme disorder. There are more than 400 million people worldwide with G6PD deficiency, and its distribution is similar to that of malaria.... -
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- A Case of Hereditary Spherocytosis with Hemolytic Anemia due to Mycoplasma pneumonia
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Na HY, Shin SH, Lee KM, Kim KN
- KMID: 2278928
- Korean J Pediatr Infect Dis.
- 2009 Dec;16(2):215-219.
Mycoplasma pneumoniae is a common cause of community-acquired pneumonia in children, with a peak incidence at 5-14 years. Extrapulmonary manifestations occur in 20-25% of patients with M. pneumoniae infection. Most... -
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- Hemolytic anemia in pediatrics
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Hah JO
- KMID: 2278471
- Korean J Pediatr.
- 2007 Jun;50(6):511-518.
- doi: 10.3345/kjp.2007.50.6.511
To understand the hemolytic anemia (HA) in children, the diagnostic approach and management of hereditary and acquired HA are described. The hereditary hemolytic anemia (HHA) can be classified according to... -
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- Hereditary Hemolytic Anemia
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Hah JO
- KMID: 2064970
- J Korean Med Assoc.
- 2006 Oct;49(10):908-919.
- doi: 10.5124/jkma.2006.49.10.908
The hereditary hemolytic anemia (HHA) can be classified into three types according to the pathogenesis: RBC membrane defects, hemoglobinopathies, and RBC enzymopathies. Clinical characteristics of these three types of HHA... -
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- Erythrocyte Band 7 Integral Protein Defect in Congenital Hemolytic Anemia: Hereditary Stomatocytosis
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Sim CS, Han SJ, Lee HJ, Park WI, Lee KJ, Chung SY, Wee S, Choi EY
- KMID: 2335230
- J Korean Pediatr Soc.
- 1997 Feb;40(2):260-265.
Hereditary stomatocytosis is a rare congenital hemolytic anemia, named after mouth shaped or stomatocytic erythrocyte morphology. In this report, we present a case of a hereditary stomatocytosis in a 1... -
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- Red Blood Cell Enzymopathies Causing Hereditary Hemolytic Anemia
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Hah JO
- KMID: 1441716
- Clin Pediatr Hematol Oncol.
- 2012 Apr;19(1):1-6.
The RBC enzyme deficiencies causing hereditary hemolytic anemia (HHA) can be divided into three groups: those participating in the glycolytic (E-M) pathway; those involved with the maintenance of a high... -
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- Treatment and Management of Late Complications in Hereditary Hemolytic Anemia
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Chueh HW
- KMID: 2168902
- Clin Pediatr Hematol Oncol.
- 2016 Apr;23(1):1-7.
- doi: 10.15264/cpho.2016.23.1.1
Hereditary hemolytic anemia is a very heterogeneous disorder in which abnormalities of red blood cell structural protein, globin protein, or enzyme defect lead to shortened life span. There has been... -
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- RBC Enzyme Analysis
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Song J
- KMID: 2049286
- Clin Pediatr Hematol Oncol.
- 2013 Apr;20(1):8-12.
Among ~20 RBC enzyme deficiencies causing hereditary hemolytic anemia (HRA), deficiencies involving three RBC enzymes such as glucose-6-phosphatase, pyruvate kinase and pyrimidine 5'-nucleodiase were known to be relatively common. The... -
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- Hereditary hemolytic anemia in Korea from 2007 to 2011: A study by the Korean Hereditary Hemolytic Anemia Working Party of the Korean Society of Hematology
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Park ES, Jung HL, Kim HJ, Park SS, Bae SH, Shin HY, Song SH, Koh KN, Lyu CJ, Lim YT, Han DK, Hah JO
- KMID: 2270708
- Blood Res.
- 2013 Sep;48(3):211-216.
- doi: 10.5045/br.2013.48.3.211
BACKGROUND: The number of patients diagnosed with hereditary hemolytic anemia (HHA) has increased since the advent of novel diagnostic techniques that accurately identify this disorder. Here, we report data from... -
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- SDS-PAGE Analysis of Red Cell Membrane Proteins in Hereditary Hemolytic Anemia
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Lee YK, Cho HI, Park SS, Ra E, Chang YH, Hur M, Lee YJ, Shin HY, Ahn HS
- KMID: 1533972
- Korean J Hematol.
- 1999 Nov;34(4):559-567.
BACKGROUND: Red cell membrane is a lipid bilayer laminated by the membrane cytoskeleton at the surface of inner monolayer. A class of hemolytic anemia, such as hereditary spherocytosis (HS) or... -
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- Hereditary Hemolytic Anemia in Korea: a Retrospective Study from 1997 to 2006
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Cho HS, Hah JO, Kang IJ, Kang HJ, Kwak JY, Koo HH, Kook H, Kim BK, Kim SK, Kim ST, Kim YD, Kim JY, Kim CS, Ghim T, Kim HS, Park SG, Park SY, Park JE, Bang SM, Seo JJ, Suh CI, Sohn SK, Shin HJ, Shin HY, Ahn HS, Oh D, Yoo ES, Lyu CJ, Yoon SS, Lee KS, Lee KC, Lee KH, Lee SY, Lee YH, Lee JA, Lee JS, Lim YT, Lim JY, Im HJ, Jeong DC, Chong SY, Chung JS, Jung HL, Cho GJ, Jo DY, Jin JY, Choi EJ, Hyun MS, Hwang PH
- KMID: 2305194
- Korean J Hematol.
- 2007 Sep;42(3):197-205.
- doi: 10.5045/kjh.2007.42.3.197
BACKGROUND: The aim of this study was to investigate the prevalence, clinical and laboratory findings of hereditary hemolytic anemia (HHA) in Korea from 1997 to 2006 and to develop the... -
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