Search Results - "Eridani, S"

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    Polycythemia: from clones to clinic by Eridani, S

    Published in Haematologica (Roma) (01-11-1993)
    “…Increasing evidence for pathological erythroid clones and availability of additional diagnostic criteria suggest to reconsider the classification of…”
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    Mast cell leukaemia: evidence for bone marrow origin of the pathological clone by Dalton, R, Chan, L, Batten, E, Eridani, S

    Published in British journal of haematology (01-10-1986)
    “…A 57-year-old female patient, admitted for an acute abdominal syndrome, was found to have an extensive proliferation of mast cells both in the peripheral blood…”
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    Primary polycythaemia: positive diagnosis using the differential response of primitive and mature erythroid progenitors to erythropoietin, interleukin 3 and alpha-interferon by Dudley, J M, Westwood, N, Leonard, S, Eridani, S, Pearson, T C

    Published in British journal of haematology (01-06-1990)
    “…Forty adult subjects were studied with the aim of establishing positive diagnostic criteria in primary proliferative polycythaemia (polycythaemia vera, PPP)…”
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    In vitro sensitivity of human erythroid progenitors to hemopoietic growth factors: studies on primary and secondary polycythemia by Montagna, C, Massaro, P, Morali, F, Foa, P, Maiolo, AT, Eridani, S

    Published in Haematologica (Roma) (01-07-1994)
    “…Laboratory of Cell Culture, National Research Council, Milan, Italy. BACKGROUND. Primary proliferative polycythemia is a clonal disease characterized by…”
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    Primary thrombocythaemia: diagnostic criteria and a simple scoring system for positive diagnosis by Dudley, J M, Messinezy, M, Eridani, S, Holland, L J, Lawrie, A, Nunan, T O, Sawyer, B, Savidge, G F, Pearson, T C

    Published in British journal of haematology (01-03-1989)
    “…Forty new patients with elevated platelet counts (greater than 600 x 10(9)/l) and without palpable splenomegaly were assigned to diagnostic groups defined by…”
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    Acute biphenotypic leukaemia (myeloid and null-ALL type) supervening in a myelodysplastic syndrome by Eridani, S, Chan, L C, Halil, O, Pearson, T C

    Published in British journal of haematology (01-11-1985)
    “…An acute leukaemia was seen in a 72-year-old patient with a myelodysplastic syndrome (MDS) of 14 months duration, who had been treated only with steroids. The…”
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    Erythropoietic colonies in a serum-free system: results in primary proliferative polycythaemia and thrombocythaemia by Eridani, S, Dudley, J M, Sawyer, B M, Pearson, T C

    Published in British journal of haematology (01-12-1987)
    “…The formation of erythropoietic colonies from the peripheral blood of normal subjects, patients with primary proliferative polycythaemia (PPP) and primary…”
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    Erythroid colony formation in primary thrombocythaemia: evidence of hypersensitivity to erythropoietin by Eridani, S, Batten, E, Sawyer, B

    Published in British journal of haematology (01-01-1984)
    “…In a group of 14 patients with primary thrombocythaemia (PT) the study of erythropoietic colony formation in vitro showed the development of so-called…”
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    Patterns of in vitro BFU-E proliferation in different forms of polycythaemia and in thrombocythaemia by Eridani, S, Sawyer, B, Pearson, T C

    Published in European journal of haematology (01-04-1987)
    “…To investigate erythroid colony formation in polycythaemia of different types and in thrombocythaemia, a study was performed in 121 subjects, including 13…”
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    Gastric non-Hodgkin's lymphoma after successful treatment of Hodgkin's disease by Eridani, S, Singh, A K

    Published in Oncology (01-01-1986)
    “…A patient seen at presentation for Hodgkin's disease (HD) at stage IV B was successfully treated with MOPP. In remission he developed coeliac disease,…”
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    Pure red cell aplasia and thymoma: demonstration of persisting inhibition of erythropoiesis after thymectomy and resolution after immune suppressive treatment by Eridani, S, Whitehead, S, Sawyer, B, Dalton, R

    Published in Clinical and laboratory haematology (01-09-1986)
    “…A 61 year-old woman presented with general malaise, hair loss, pure red cell aplasia (PRCA) and thymoma: no growth of erythropoietic colonies in vitro (BFU-E)…”
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