Search Results - "Belhani, M"

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    Epidemiological and immunochemical parameters of monoclonal plasma cell dyscrasias of 2121 cases in Algeria by Belouni, R., Allam, I., Cherguelaine, K., Berkani, L., Belaid, B., Berkouk, Y., Nekkal, S., Saidani, M., Belhani, M., Ghaffor, M., Djidjik, R.

    Published in Current research in translational medicine (01-04-2020)
    “…Plasma cell dyscrasias (PCD) are a heterogeneous group of diseases characterized by the expansion of monoclonal bone marrow plasma cells that produce a…”
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    Journal Article
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    Establishing a harmonized haemophilia registry for countries with developing health care systems by Alzoebie, A., Belhani, M., Eshghi, P., Kupesiz, A. O., Ozelo, M., Pompa, M. T., Potgieter, J., Smith, M.

    “…Summary Over recent decades tremendous progress has been made in diagnosing and treating haemophilia and, in resource‐rich countries, life expectancy of people…”
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    IgD multiple myeloma: Clinical, biological features and prognostic value of the serum free light chain assay by Djidjik, R., Lounici, Y., Chergeulaïne, K., Berkouk, Y., Mouhoub, S., Chaib, S., Belhani, M., Ghaffor, M.

    Published in Pathologie biologie (Paris) (01-09-2015)
    “…IgD multiple myeloma (MM) is a rare subtype of myeloma, it affects less than 2% of patients with MM. To evaluate the clinical and prognostic attributes of…”
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    High-dose salvage chemotherapy without bone marrow transplantation for adult patients with refractory Hodgkin's disease by Tourani, J M, Levy, R, Colonna, P, Desablens, B, Leprise, P Y, Guilhot, F, Brahimi, S, Belhani, M, Ifrah, N, Sensebe, L

    Published in Journal of clinical oncology (01-07-1992)
    “…For patients with Hodgkin's disease (HD) who do not achieve complete response (CR), who experience a relapse within the first year of CR, and for those who…”
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    Partial splenectomy in homozygous beta thalassaemia by de Montalembert, M, Girot, R, Revillon, Y, Jan, D, Adjrad, L, Ardjoun, F Z, Belhani, M, Najean, Y

    Published in Archives of disease in childhood (01-03-1990)
    “…Partial splenectomy was performed on 30 patients with homozygous beta thalassaemia to reduce blood requirements and to avoid the risk of overwhelming…”
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    Indication de la transfusion sanguine chez les SDM by Ferroudj, N., Bensadok, M., Ramaoun, M., Belhani, M., Nekkal, S.

    “…La drépanocytose est responsable de nombreux complications : les crises vaso-occlusives, l’hémolyse aiguë, le STA, l’AVC. La transfusion sanguine constitue…”
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    Indirect evaluation of a gene frequency: calculation of beta-thalassemia frequency in Algeria based on associated hemoglobin variants frequency by Bachir, D, Belhani, M, Godet, J, Nigon, V, Colonna, P

    Published in Human heredity (01-01-1984)
    “…The gene frequency (q) of beta-thalassemia (T) is more difficult to evaluate directly than the frequency of hemoglobin variants (V), Hb S and Hb C being the…”
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    Hemoglobin H disease from Algeria: genetic and molecular characterization by Tabone, P, Henni, T, Belhani, M, Colonna, P, Verdier, G, Godet, J

    Published in Acta haematologica (1981)
    “…A case of Hb H disease from Algeria was studied at the genetic and molecular level in order to delineate the pattern of alpha-thalassemia in the Mediterranean…”
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