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Journal Abstract Search

130 related items for PubMed ID: 9414642

  • 1.
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  • 2. Composition of the intra-erythroblastic precipitates in thalassaemia and congenital dyserythropoietic anaemia (CDA): identification of a new type of CDA with intra-erythroblastic precipitates not reacting with monoclonal antibodies to alpha- and beta-globin chains.
    Wickramasinghe SN, Lee MJ, Furukawa T, Eguchi M, Reid CD.
    Br J Haematol; 1996 Jun; 93(3):576-85. PubMed ID: 8652376
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  • 3. Erythroblastic inclusions in dominantly inherited beta thalassemias.
    Ho PJ, Wickramasinghe SN, Rees DC, Lee MJ, Eden A, Thein SL.
    Blood; 1997 Jan 01; 89(1):322-8. PubMed ID: 8978308
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  • 4. The fate of excess beta-globin chains within erythropoietic cells in alpha-thalassaemia 2 trait, alpha-thalassaemia 1 trait, haemoglobin H disease and haemoglobin Q-H disease: an electron microscope study.
    Wickramasinghe SN, Hughes M, Fucharoen S, Wasi P.
    Br J Haematol; 1984 Mar 01; 56(3):473-82. PubMed ID: 6320861
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  • 5. Red cell volume distribution curves and intracellular globin chain precipitation in the alpha-thalassaemic mouse, Hbath-J.
    Wickramasinghe SN, Rayfield LS, Brent L.
    Br J Exp Pathol; 1986 Feb 01; 67(1):73-83. PubMed ID: 3004553
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  • 6. Evidence that the ubiquitin proteolytic pathway is involved in the degradation of precipitated globin chains in thalassaemia.
    Wickramasinghe SN, Lee MJ.
    Br J Haematol; 1998 May 01; 101(2):245-50. PubMed ID: 9609517
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  • 7. Severe inclusion body beta-thalassaemia with haemolysis in a patient double heterozygous for beta(0)-thalassaemia and quadruplicated alpha-globin gene arrangement of the anti-4.2 type.
    Beris P, Solenthaler M, Deutsch S, Darbellay R, Tobler A, Bochaton-Pialat ML, Gabbiani G.
    Br J Haematol; 1999 Jun 01; 105(4):1074-80. PubMed ID: 10554822
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  • 8. Globin chain precipitation, deranged iron metabolism and dyserythropoiesis in some thalassaemia syndromes.
    Wickramasinghe SN, Hughes M.
    Haematologia (Budap); 1984 Jun 01; 17(1):35-55. PubMed ID: 6327469
    [Abstract] [Full Text] [Related]

  • 9. Ultrastructural studies of erythropoiesis in beta-thalassaemia trait.
    Wickramasinghe SN, Hughes M.
    Br J Haematol; 1980 Nov 01; 46(3):401-7. PubMed ID: 6255979
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  • 12. Globin chain turnover in reticulocytes from patients with beta (0) -thalassaemia/Hb E disease.
    Kalpravidh RW, Komolvanich S, Wilairat P, Fucharoen S.
    Eur J Haematol; 1995 Nov 01; 55(5):322-6. PubMed ID: 7493679
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  • 14. Studies of erythropoietic cells in heterozygotes and homozygotes for haemoglobin Constant Spring and in heterozygotes for both haemoglobin Constant Spring and alpha-thalassaemia 1 trait: extent of globin chain precipitation and cell cycle distribution.
    Wickramasinghe SN, Fucharoen S, Wasi P.
    Clin Lab Haematol; 1986 Nov 01; 8(3):187-98. PubMed ID: 3757450
    [Abstract] [Full Text] [Related]

  • 15. Beta globin messenger RNA content of bone marrow erythroblasts in heterozygous beta-thalassemia.
    Benz EJ, Pritchard J, Hillman D, Glass J, Forget BG.
    Am J Hematol; 1984 Jan 01; 16(1):33-45. PubMed ID: 6695907
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  • 18. Electron microscope and high resolution autoradiographic studies of the erythroblasts in haemoglobin H disease.
    Wickramasinghe SN, Hughes M, Hollán SR, Horányi M, Szelényi J.
    Br J Haematol; 1980 Jul 01; 45(3):401-4. PubMed ID: 6252941
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  • 19. Heterozygous beta thalassaemia of unusual severity.
    Friedman S, Ozsoylu S, Luddy R, Schwartz E.
    Br J Haematol; 1976 Jan 01; 32(1):65-77. PubMed ID: 1259927
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