Diagnosis of megaloblastic anaemias von Wickramasinghe, S.N.

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DYSERYTHROPOIESIS AND CONGENITAL DYSERYTHROPOIETIC ANAEMIAS von WICKRAMASINGHE, S. N.

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Blood and bone marrow changes in malaria von Wickramasinghe, S.N., Abdalla, S.H.

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Congenital dyserythropoietic anaemias: clinical features, haematological morphology and new biochemical data von Wickramasinghe, S.N.

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Bone marrow cells from vitamin B12- and folate-deficient patients misincorporate uracil into DNA von WICKRAMASINGHE, S. N, FIDA, S

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ROLE OF MACROPHAGES IN ACETAMINOPHEN (PARACETAMOL)-INDUCED HEPATOTOXICITY von GOLDIN, R. D., RATNAYAKA, I. D., BREACH, C. S., BROWN, I. N., WICKRAMASINGHE, S. N.

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Severe congenital dyserythropoietic anaemia type I: prenatal management, transfusion support and alpha‐interferon therapy von Parez, N., Dommergues, M., Zupan, V., Chambost, H., Fieschi, J. B., Delaunay, J., Miélot, F., Cramer, E. M., Dommergues, J.‐P., Wickramasinghe, S. N., Tchernia, G.

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Demonstration of mRNA for five species of cytochrome P450 in human bone marrow, bone marrow‐derived macrophages and human haemopoietic cell lines von Hodges, Vivien M., Molloy, Gael Y., Wickramasinghe

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Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage von Blount, B.C. (University of California, Berkeley, CA.), Mack, M.M, Wehr, C.M, MacGregor, J.T, Hiatt, R.A, Wang, G, Wickramasinghe, S.N, Everson, R.B, Ames, B.N

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Congenital dyserthropoietic anaemia other than type I to III with a peculiar erythroblastic morphology von Woessner, S., Trujillo, M., Florensa, L., Mesa, M. C., Wickramasinghe, S. N.

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Determinants of iron status and bilirubin levels in congenital dyserythropoietic anaemia type I von WICKRAMASINGHE, S. N, THEIN, S. L, SRICHAIRATANAKOOL, S, PORTER, J. B

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Effects of four species of interferon‐α on cultured erythroid progenitors from congenital dyserythropoietic anaemia type I von MENIKE, D, WICKRAMASINGHE, S. N

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Apoptotic bodies in a murine model of alcoholic liver disease: Reversibility of ethanol-induced changes von Goldin, R. D., Hunt, N. C., Clark, J., Wickramasinghe, S. N.

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Hereditary sideroblastic anaemia due to a mutation in exon 10 of the erythroid 5‐aminolaevulinate synthase gene von EDGAR, A. J, WICKRAMASINGHE, S. N

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Evidence that the ubiquitin proteolytic pathway is involved in the degradation of precipitated globin chains in thalassaemia von WICKRAMASINGHE, S. N, LEE, M. J

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Changes in murine bone marrow macrophages and erythroid burst-forming cells following the intravenous injection of liposome-encapsulated dichloromethylene diphosphonate (Cl2MDP) von Giuliani, A. L., Wiener, E., Lee, M. J., Brown, I. N., Berti, G., Wickramasinghe, S. N.

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Stearate inhibition of breast cancer cell proliferation. A mechanism involving epidermal growth factor receptor and G-proteins von Wickramasinghe, NS, Jo, H, McDonald, JM, Hardy, RW

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Limited value of serum holo-transcobalamin II measurements in the differential diagnosis of macrocytosis von Wickramasinghe, S N, Ratnayaka, I D

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Correlations between holo-transcobalamin II, holo-haptocorrin, and total B12 in serum samples from healthy subjects and patients von Wickramasinghe, S N, Fida, S

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Cell-specific mitotic defect and dyserythropoiesis associated with erythroid band 3 deficiency von Zon, Leonard I, Paw, Barry H, Davidson, Alan J, Zhou, Yi, Li, Rong, Pratt, Stephen J, Lee, Charles, Trede, Nikolaus S, Brownlie, Alison, Donovan, Adriana, Liao, Eric C, Ziai, James M, Drejer, Anna H, Guo, Wen, Kim, Carol H, Gwynn, Babette, Peters, Luanne L, Chernova, Marina N, Alper, Seth L, Zapata, Agustin, Wickramasinghe, Sunitha N, Lee, Matthew J, Lux, Samuel E, Fritz, Andreas, Postlethwait, John H

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