These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

120 related items for PubMed ID: 2081381

  • 1. Ultrastructural abnormalities and arrest of protein biosynthesis in some erythroblasts from homozygotes for haemoglobin C and double heterozygotes for haemoglobin C and beta-thalassaemia.
    Wickramasinghe SN.
    Clin Lab Haematol; 1990; 12(4):401-8. PubMed ID: 2081381
    [Abstract] [Full Text] [Related]

  • 2. Dyserythropoiesis in homozygous haemoglobin C disease.
    Wickramasinghe SN, Akinyanju OO, Hughes M.
    Clin Lab Haematol; 1982; 4(4):373-81. PubMed ID: 7166023
    [Abstract] [Full Text] [Related]

  • 3. Ultrastructure and cell cycle distribution of erythropoietic cells in heterozygotes and homozygotes for haemoglobin E.
    Wickramasinghe SN, Hughes M, Wasi P, Fucharoen S, Litwinczuk RA.
    Br J Haematol; 1984 Aug; 57(4):685-94. PubMed ID: 6743574
    [Abstract] [Full Text] [Related]

  • 4. Ineffective erythropoiesis in haemoglobin E beta -thalassaemia: an electron microscope study.
    Wickramasinghe SN, Hughes M, Wasi P, Fucharoen S, Modell B.
    Br J Haematol; 1981 Jul; 48(3):451-7. PubMed ID: 7259993
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. 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; 56(3):473-82. PubMed ID: 6320861
    [Abstract] [Full Text] [Related]

  • 8. Ultrastructural studies of erythropoiesis in beta-thalassaemia trait.
    Wickramasinghe SN, Hughes M.
    Br J Haematol; 1980 Nov; 46(3):401-7. PubMed ID: 6255979
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Haemoglobin synthesis in bone marrow of patients with beta O and beta +-thalassaemia.
    Musumeci S, Schilirò G, Romeo MA, Pizzarelli G, Fischer A, Russo G.
    Acta Haematol; 1981 Nov; 65(3):170-6. PubMed ID: 6785970
    [Abstract] [Full Text] [Related]

  • 12. Studies of erythroblast function in congenital dyserythropoietic anaemia, type I: evidence of impaired DNA, RNA, and protein synthesis and unbalanced globin chain synthesis in ultrastructurally abnormal cells.
    Wickramasinghe SN, Pippard MJ.
    J Clin Pathol; 1986 Aug; 39(8):881-90. PubMed ID: 2427549
    [Abstract] [Full Text] [Related]

  • 13. Some aspects of the biology of multinucleate and giant mononucleate erythroblasts in a patient with CDA, type III.
    Wickramasinghe SN, Goudsmit R.
    Br J Haematol; 1979 Apr; 41(4):485-95. PubMed ID: 435398
    [Abstract] [Full Text] [Related]

  • 14. [Double heterozygote HbC-beta(O) thalassemia. A new case of this combination in a Caucasian subject].
    Vives Corrons JL, Vallespí MT, Jou JM, Aguilar i Basocompte JL.
    Sangre (Barc); 1983 Apr; 28(5):656-62. PubMed ID: 6665699
    [No Abstract] [Full Text] [Related]

  • 15. Some features of bone marrow macrophages in patients with homozygous beta-thalassaemia.
    Wickramasinghe SN, Hughes M.
    Br J Haematol; 1978 Jan; 38(1):23-8. PubMed ID: 205237
    [Abstract] [Full Text] [Related]

  • 16. Hereditary haemoglobin disorders in Brazil.
    Zago MA, Costa FF.
    Trans R Soc Trop Med Hyg; 1985 Jan; 79(3):385-8. PubMed ID: 3898485
    [Abstract] [Full Text] [Related]

  • 17. Electron microscope autoradiographic studies of the erythroblasts of a case of congenital dyserythropoietic anaemia, type II.
    Wickramasinghe SN, Parry TE, Hughes M.
    Scand J Haematol; 1978 May; 20(5):429-39. PubMed ID: 663556
    [Abstract] [Full Text] [Related]

  • 18. Pregnancy in abnormal haemoglobins CC, S-thalassaemia, SF, CF, double heterozygotes.
    Hendrickse JP, Harrison KA, Watson-Williams EJ, Luzzatto L, Ajabor LN.
    J Obstet Gynaecol Br Commonw; 1972 May; 79(5):410-5. PubMed ID: 4537546
    [No Abstract] [Full Text] [Related]

  • 19. Observations on the relationship between gamma-globin chain content and globin chain precipitation in thalassaemic erythroblasts and on the composition of erythroblastic inclusions in HbE/beta-thalassaemia.
    Wickramasinghe SN, Lee MJ.
    Eur J Haematol; 1997 Nov; 59(5):305-9. PubMed ID: 9414642
    [Abstract] [Full Text] [Related]

  • 20. Evidence for posttranslational control of Hb C synthesis in an individual with Hb C trait and alpha-thalassemia.
    Liebhaber SA, Cash FE, Cornfield DB.
    Blood; 1988 Feb; 71(2):502-4. PubMed ID: 3337909
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.