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Treatment and Management of Late Complications in Hereditary Hemolytic Anemia

Chueh HW

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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Glucose-6-phosphate Dehydrogenase Deficiency

Lee JM

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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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

Park ES, Jung HL, Kim HJ, Park SS, Bae SH, Shin HY, Song SH, Koh KN, Lyu CJ, Lim YT, Han DK, Hah JO

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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RBC Enzyme Analysis

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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A new paradigm in the diagnosis of hereditary hemolytic anemia

Jung HL

No abstract available.
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Red Blood Cell Enzymopathies Causing Hereditary Hemolytic Anemia

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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A Case of Hereditary Spherocytosis with Hemolytic Anemia due to Mycoplasma pneumonia

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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A Case of Congenital Hemolytic Anemia of Unknown Cause Combined with Gilbert's Syndrome

Lim JW, Choi JH, Nam YH, Seo IS, Yoon SM, Koo MS

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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Hereditary Hemolytic Anemia in Korea: a Retrospective Study from 1997 to 2006

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

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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Hemolytic anemia in pediatrics

Hah JO

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

Hah JO

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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SDS-PAGE Analysis of Red Cell Membrane Proteins in Hereditary Hemolytic Anemia

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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Erythrocyte Band 7 Integral Protein Defect in Congenital Hemolytic Anemia: Hereditary Stomatocytosis

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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A Case of Congenital Nonspherocytic Hemolytic Anemia

Kim TS, Jeon SB, Pyun BY

  • KMID: 1676260
  • J Korean Pediatr Soc.
  • 1985 Jun;28(6):597-603.
No abstract available.
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