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Volumn 4, Issue 2, 1997, Pages 75-78

Pathobiology of thalassemic erythrocytes

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLOBIN; BETA GLOBIN; HEMOGLOBIN E; HEMOGLOBIN H; HEMOGLOBIN VARIANT; SYNAPSIN II;

EID: 0030908559     PISSN: 10656251     EISSN: None     Source Type: Journal    
DOI: 10.1097/00062752-199704020-00001     Document Type: Short Survey
Times cited : (38)

References (19)
  • 1
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    • Thalassemia: A global public health problem
    • Weatherall DJ, Clegg JB: Thalassemia: a global public health problem. Nature Med 1996, 2:847-849. A brief, thoughtful look at the emerging importance of the thalassemias as worldwide health problems.
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    • Weatherall, D.J.1    Clegg, J.B.2
  • 2
    • 0029897441 scopus 로고    scopus 로고
    • Hematologic disorders in children from Southeast Asia
    • Glader BE, Look KA: Hematologic disorders in children from Southeast Asia. Pediatr Hematol 1996, 43:665-681.
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    • Glader, B.E.1    Look, K.A.2
  • 4
    • 0028264172 scopus 로고
    • Thalassemia: Pathophysiology of red cell changes
    • Schrier SL: Thalassemia: pathophysiology of red cell changes. Annu Rev Wed 1994, 45:211-218.
    • (1994) Annu Rev Wed , vol.45 , pp. 211-218
    • Schrier, S.L.1
  • 5
    • 0026704541 scopus 로고
    • Isolation, characterization, and immunoprecipitation studies of immune complexes from membranes of β-thalassemic erythrocytes
    • Yuan J, Kannan R, Shinar E, Rachmilewitz EA, Low PS: Isolation, characterization, and immunoprecipitation studies of immune complexes from membranes of β-thalassemic erythrocytes. Blood 1992, 79:3007-3013.
    • (1992) Blood , vol.79 , pp. 3007-3013
    • Yuan, J.1    Kannan, R.2    Shinar, E.3    Rachmilewitz, E.A.4    Low, P.S.5
  • 7
    • 0029097965 scopus 로고
    • Deferiprone (L1) chelates pathologic iron deposits from membranes of intact thalassemic and sickle red blood cells both in vitro and in vivo
    • Shalev O, Repka T, Goldfarb A, Grinberg L, Abrahamov A, Olivieri NF, Rachmilewitz EA, Hebbel RP: Deferiprone (L1) chelates pathologic iron deposits from membranes of intact thalassemic and sickle red blood cells both in vitro and in vivo. Blood 1995, 86:2006-2013. Chelation of iron in vivo and in vitro appears to ameliorate oxidant injury in β-thalassemic erythrocytes.
    • (1995) Blood , vol.86 , pp. 2006-2013
    • Shalev, O.1    Repka, T.2    Goldfarb, A.3    Grinberg, L.4    Abrahamov, A.5    Olivieri, N.F.6    Rachmilewitz, E.A.7    Hebbel, R.P.8
  • 11
    • 0027161045 scopus 로고
    • Phosphatidylserine in the outer leaflet of red blood cells from β-thalassemia patients may explain the chronic hypercoagulable state and thrombotic episodes
    • Borenstein-Ben Yashar V, Barenholz Y, Hy-Am E, Rachmilewitz EA, Eldor A: Phosphatidylserine in the outer leaflet of red blood cells from β-thalassemia patients may explain the chronic hypercoagulable state and thrombotic episodes. Am J Hematol 1993, 44:63-65.
    • (1993) Am J Hematol , vol.44 , pp. 63-65
    • Borenstein-Ben Yashar, V.1    Barenholz, Y.2    Hy-Am, E.3    Rachmilewitz, E.A.4    Eldor, A.5
  • 14
    • 0029816461 scopus 로고    scopus 로고
    • Interaction of hemoglobin e and pyrimidine 5' nucleotidase deficiency
    • Rees DC, Duley J, Simmonds HA, Wonke B, Thein SL, Clegg JB, Weatherall DJ: Interaction of hemoglobin E and pyrimidine 5' nucleotidase deficiency. Blood 1996, 88:2761-2767. This family study provides a clue as to why the HbE/β-thalassemia syndrome can produce such severe anemia.
    • (1996) Blood , vol.88 , pp. 2761-2767
    • Rees, D.C.1    Duley, J.2    Simmonds, H.A.3    Wonke, B.4    Thein, S.L.5    Clegg, J.B.6    Weatherall, D.J.7
  • 18
    • 0027181636 scopus 로고
    • Accelerated programmed cell death (apoptosis) in erythroid precursors of patients with severe β-thalassemia (Cooley's anemia)
    • Yuan J, Angelucci E, Lucarelli G, Aljurf M, Snyder LM, Kiefer CR, Ma L, Schrier SL: Accelerated programmed cell death (apoptosis) in erythroid precursors of patients with severe β-thalassemia (Cooley's anemia). Blood 1993, 82:374-377.
    • (1993) Blood , vol.82 , pp. 374-377
    • Yuan, J.1    Angelucci, E.2    Lucarelli, G.3    Aljurf, M.4    Snyder, L.M.5    Kiefer, C.R.6    Ma, L.7    Schrier, S.L.8
  • 19
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    • Abnormal assembly of membrane proteins in erythroid progenitors of patients with β-thalassemia major
    • Aljurf M, Ma L, Angelucci E, Lucarelli G, Snyder LM, Kiefer CR, Yuan J, Schrier SL: Abnormal assembly of membrane proteins in erythroid progenitors of patients with β-thalassemia major. Blood 1996, 87:2049-2056. Further emphasizes the importance of studies of marrow in severe β-thalassemia.
    • (1996) Blood , vol.87 , pp. 2049-2056
    • Aljurf, M.1    Ma, L.2    Angelucci, E.3    Lucarelli, G.4    Snyder, L.M.5    Kiefer, C.R.6    Yuan, J.7    Schrier, S.L.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.