Search Results - "SEWELL, W. A"

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    Is dosing of therapeutic immunoglobulins optimal? A review of a three-decade long debate in europe by Kerr, Jacqueline, Quinti, Isabella, Eibl, Martha, Chapel, Helen, Späth, Peter J, Sewell, W A Carrock, Salama, Abdulgabar, van Schaik, Ivo N, Kuijpers, Taco W, Peter, Hans-Hartmut

    Published in Frontiers in immunology (12-12-2014)
    “…The consumption of immunoglobulins (Ig) is increasing due to better recognition of antibody deficiencies, an aging population, and new indications. This review…”
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    CD200 is a useful diagnostic marker for identifying atypical chronic lymphocytic leukemia by flow cytometry by Ting, Y. S., Smith, S. A. B. C., Brown, D. A., Dodds, A. J., Fay, K. C., Ma, D. D. F., Milliken, S., Moore, J. J., Sewell, W. A.

    “…Introduction Immunophenotyping by flow cytometry is routinely employed in distinguishing between chronic lymphocytic leukemia (CLL) and mantle cell lymphoma…”
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    European consensus proposal for immunoglobulin therapies by Sewell, W. A. Carrock, Kerr, Jacqueline, Behr‐Gross, Marie‐Emmanuelle, Peter, Hans‐Hartmut

    Published in European journal of immunology (01-08-2014)
    “…The use of immunoglobulin (Ig) preparations (intravenous, IVIg, subcutaneous, SCIg) for replacement and immunomodulation therapy worldwide has tripled in the…”
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    Transitional B cell subsets in human bone marrow by Agrawal, S., Smith, S. A. B. C., Tangye, S. G., Sewell, W. A.

    Published in Clinical and experimental immunology (01-10-2013)
    “…Summary B cells originate from precursors in the bone marrow, and the first cells which migrate to the peripheral blood have been classified as ‘transitional B…”
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    Do ribosomopathies explain some cases of common variable immunodeficiency by Khan, S, Pereira, J, Darbyshire, P.J, Holding, S, Doré, P.C, Sewell, W.A.C, Huissoon, A

    Published in Clinical and experimental immunology (01-01-2011)
    “…The considerable clinical heterogeneity of patients with common variable immunodeficiency disorders (CVID) shares some similarity with bone-marrow failure…”
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    Antibody deficiency by Herriot, R, Sewell, W A C

    Published in Journal of clinical pathology (01-09-2008)
    “…Antibody deficiencies may arise as primary disorders or secondary to a variety of diseases, drugs and other environmental/iatrogenic factors. Significant…”
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    Clinical Immunology Review Series: An approach to the use of the immunology laboratory in the diagnosis of clinical allergy by Williams, P, Sewell, W.A.C, Bunn, C, Pumphrey, R, Read, G, Jolles, S

    Published in Clinical and experimental immunology (01-07-2008)
    “…In the last 10 years UK immunology laboratories have seen a dramatic increase in the number and range of allergy tests performed. The reasons for this have…”
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    Limited value of testing for intrinsic factor antibodies with negative gastric parietal cell antibodies in pernicious anaemia by Khan, S, Del-Duca, C, Fenton, E, Holding, S, Hirst, J, Doré, P C, Sewell, W A C

    Published in Journal of clinical pathology (01-05-2009)
    “…The appropriate testing strategy for diagnosing pernicious anaemia using gastric parietal cell (GPC) and/or intrinsic factor antibodies (IFA) is controversial…”
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    IgE Sequences in Individuals Living in an Area of Endemic Parasitism Show Little Mutational Evidence of Antigen Selection by Wang, Y., Jackson, K. J. L., Chen, Z., Gaëta, B. A., Siba, P. M., Pomat, W., Walpole, E., Rimmer, J., Sewell, W. A., Collins, A. M.

    Published in Scandinavian journal of immunology (01-05-2011)
    “…Patterns of somatic mutation in IgE genes from allergic individuals have been a focus of study for many years, but IgE sequences have never been reported from…”
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    Secondary systemic lupus erythematosus: An analysis of 4 cases of uncontrolled hereditary angioedema by Khan, Sujoy, Tarzi, Michael D, Doré, Philip C, Sewell, W.A.C, Longhurst, Hilary J

    Published in Clinical Immunology (01-04-2007)
    “…Abstract The association of systemic lupus erythematosus and hereditary angioedema (HAE) has formed the basis of numerous case reports and is hypothesised to…”
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    Deficiency in circulating natural killer (NK) cell subsets in common variable immunodeficiency and X‐linked agammaglobulinaemia by Aspalter, R. M., Sewell, W. A. C., Dolman, K., Farrant, J., Webster, A. D. B.

    Published in Clinical and experimental immunology (01-09-2000)
    “…Absolute and relative NK cell numbers were determined in peripheral whole blood by flow cytometry in patients with common variable immunodeficiency (CVID) (n =…”
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    Some cases of common variable immunodeficiency may be due to a mutation in the SBDS gene of Shwachman-Diamond syndrome by Khan, S, Hinks, J, Shorto, J, Schwarz, M.J, Sewell, W.A.C

    Published in Clinical and experimental immunology (01-03-2008)
    “…Known genetic defects currently account for only a small proportion of patients meeting criteria for 'probable' or 'possible' common variable immunodeficiency…”
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    The clinical significance of antinucleolar antibodies by Khan, S, Alvi, A, Holding, S, Kemp, M L, Raine, D, Doré, P C, Sewell, W A C

    Published in Journal of clinical pathology (01-03-2008)
    “…The importance of antinucleolar antibodies seen by indirect immunofluorescence on HEp-2 cells, although associated with systemic sclerosis (SSc), in unselected…”
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    A two-phase pathogenesis of graft-versus-host disease in mice by VAN LEEUWEN, L, GUIFFRE, A, ATKINSON, K, RAINER, S. P, SEWELL, W. A

    “…Activation of donor T cells is required for the development of graft-versus-host disease (GVHD), a major complication of bone marrow transplantation. We…”
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    Therapeutic strategies in common variable immunodeficiency by SEWELL, W. A, BUCKLAND, Matthew S, JOLLES, Stephen R. A

    Published in Drugs (New York, N.Y.) (01-01-2003)
    “…The treatment of common variable immunodeficiency (CVID) is currently based on the early recognition of the condition and replacement immunoglobulin combined…”
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    Immunomodulatory action of intravenous immunoglobulin by Sewell, W. A. C., Jolles, S.

    Published in Immunology (01-12-2002)
    “…Intravenous immunoglobulin (IVIg) is a blood product prepared from the serum of between 1000 and 15 000 donors per batch. It is the treatment of choice for…”
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